Classifications

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  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
  • A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
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  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
  • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
  • A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
• • A—HUMAN NECESSITIES
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  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
  • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
  • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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  • A61K31/555—Heterocyclic compounds containing heavy metals, e.g. hemin, hematin, melarsoprol
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  • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
  • A61K31/7028—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages
  • A61K31/7034—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin
  • A61K31/704—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin
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  • A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
  • A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
  • A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
  • A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
  • A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
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  • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
• • A—HUMAN NECESSITIES
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  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
  • A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
• • A—HUMAN NECESSITIES
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  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
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• • A—HUMAN NECESSITIES
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  • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
  • A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
• • A—HUMAN NECESSITIES
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Definitions

• the present invention provides methods and compositions for treating cancer with hypoxia activated prodrugs administered alone and in combination with anticancer drugs that are not hypoxically activated and/or in combination with radiation therapy
• the invention relates to the fields of medicine, pharmacology, and medicinal chemistry
• HAPs hypoxia-activated prodrugs
• TH-302 and TH-281 are particularly promising therapeutic candidates TH-302, known by the chemical name (2- bromoethyl)( ⁇ [(2-bromoethyl)am ⁇ no][(2-n ⁇ tro-3-methyl ⁇ m ⁇ dazol-4- yl)methoxy]phosphoryl ⁇ )am ⁇ ne, has the structure represented below
• TH-281 which differs from TH-302 only in that it has 2-chJoroethyl groups instead of the 2-bromoethyl groups present in TH- 302
• the present invention provides a stable liquid composition
• TH-302 or another compound of Formula I (10 mg/mL to about 300 mg/mL), ethanol (70%-95%), a nonionic surfactant such as TWEEN 80 (5%-10%), and optionally one or more other agents, such as dimethylacetamide.
• the present invention provides methods for treating cancer in a patient with TH-302 or another compound of Formula I 1 which methods comprise administering to a patient in need of cancer therapy TH-302 or another compound of Formula I as a single agent (i.e., in monotherapy, where no other anticancer agents are administered during the course of therapy with TH-302 or other compound of Formula I) at a dose in the range of 240 mg/m 2 to 1 g/m 2 .
• the therapeutically effective dose is administered once per week for at least three weeks.
• the therapeutically effective dose is administered once per week for three weeks, no dose is administered during the fourth week (four weeks being one "cycle"), and this pattern of administration is followed for one or more additional cycles
• the therapeutically effective dose is administered once every three weeks, and this pattern of administration is followed for one or more additional cycles
• the dose administered once per week is 480 mg/m 2 , 575 mg/m 2 , or 670 mg/m 2 .
• the cancer is small cell lung cancer (SCLC), including but not limited to refractory SCLC, or melanoma
• SCLC small cell lung cancer
• the invention provides a method of treating cancer by administering TH-302 as a single agent, wherein said TH-302 is administered intravenously in an amount in the range of 200 mg/m 2 to 700 mg/m 2 to a patient in need of cancer therapy, e.g , treatment for a small cell lung cancer or melanoma
• the invention provides administering TH-302 monotherapy to a patient with small cell lung cancer.
• the TH-302 is administered once per week for 3 weeks followed by one week with no administration (e.g., days 1 , 8 and 15 of a 28-day cycle)
• the TH-302 is administered to a patient with small cell lung cancer once per week for 3 weeks followed by one week with no administration at a dose in the range of about 480 mg/m 2 - about 670 mg/m 2 .
• the TH-302 is administered for at least 2, at least 3, at least 4, at least 5, or at least 6 28-day cycles.
• the TH-302 is administered once every three weeks (e g , day 1 of a 21 -day cycle). In some embodiments the TH-302 is administered to a patient with small cell lung cancer once every 3 weeks at a dose in the range of about 670 mg/m 2 - less than 940 mg/m 2 . In some embodiments the TH-302 is administered for at least 2, at least 3, at least 4, at least 5, or at least 6 21 -day cycles.
• the invention provides administering TH-302 monotherapy to a patient with metastatic melanoma
• the TH-302 is administered once per week for 3 weeks followed by one week with no administration (e g , days 1 , 8 and 15 of a 28-day cycle)
• the TH-302 is administered at a dose in the range of about 480 mg/m 2 - about 670 mg/m 2 , sometimes about 575 mg/m 2 - about 670 mg/m 2
• the TH-302 is administered for at least 2, at least 3, at least 4, at least 5, or at least 6, 28-day cycles
• the present invention provides methods for treating cancer in which the patient is administered TH-302 (or another compound of Formula I) in combination with an oral and/or topical formulation of an agent to reduce or prevent mucosal and/or skin damage
• the present invention provides new methods for administering a hypoxia-activated prodrug (HAP) and a second anticancer agent that is not a HAP According to these methods, the two drugs are administered noncontemporaneously, with administration of the non-HAP drug commencing a specified time after the completion of HAP administration
• HAP hypoxia-activated prodrug
• the invention provides methods for treating cancer in which a patient in need of cancer therapy is administered TH-302 or another compound of Formula I in combination with a non-HAP anticancer agent
• the non-HAP anticancer agent is gemcitabine, docetaxel, pemetrexed, or doxorubicin
• the cancer is pancreatic cancer, prostate cancer non-SCLC (NSCLC), or sarcoma
• the cancer is pancreatic cancer and the non-HAP anticancer agent is gemcitabine
• the cancer is prostate cancer
• the non-HAP anticancer agent is docetaxel
• the cancer is NSCLC
• the non-HAP anticancer agent is docetaxel or pemetrexed in one embodiment
• the cancer is sarcoma
• the non-HAP anticancer agent is doxorubicin
• the invention provides a method of treating cancer by administering a therapeutically effective dose of
• the patient is in need of treatment for NSCLC, prostate cancer, neuroendocrine cancer, anal cancer, urachal cancer urethral cancer breast cancer, melanoma, and renal cell carcinoma and the anticancer drug that is not a hypoxia activated prodrug is docetaxel, or
• the patient is in need of treatment for bile duct cancer, ovarian cancer, esophageal cancer, pancreatic cancer, NSCLC, ampullary cancer, neuroendocrine cancer, soft tissue sarcoma, and thyroid cancer and the anticancer drug that is not a hypoxia activated prodrug is gemcitabine, or
• the patient is in need of treatment for esophageal cancer pancreatic cancer, NSCLC neuroendocrine cancer, soft tissue sarcoma, colorectal cancer, hepatocellular carcinoma (HCC), renal cancer, and parotid cancer and the anticancer drug that is not a hypoxia activated prodrug is pemetrexed
• the invention provides a method of treating cancer by administering TH-302 and a therapeutically effective dose of an anticancer drug that is not a hypoxia activated prodrug to a patient in need of cancer therapy, wherein TH-302 is administered intravenously in an amount in the range of 200 mg/m 2 to 500 mg/m 2 and administration of the anticancer drug that is not a hypoxia activated prodrug begins 30 minutes to 8 hours, optionally 2 hours to 6 hours, after administration of TH-302 is completed
• Section I provides definitions of certain terms used herein
• Section Il describes pharmaceutical formulations of TH-302, TH-281, and other compounds of Formula I provided by the invention
• Section III describes methods for treating cancer with TH-302 TH-281 , and other compounds of Formula I in single agent therapies (monotherapies) provided by the invention
• Section IV describes methods for treating cancer with a HAP and non-HAP anticancer agents in combination
• Section V describes methods for treating cancer with TH-302, TH-281, and other compounds of Formula I in combination with non-HAP anticancer agents
• Section V is followed by examples that provide illustrative embodiments of the methods and compositions provided by the invention
• “About” as used herein is used to provide flexibility to a numerical range endpoint by providing that a given value may be “a little above” or “a little below” the endpoint accounting for variations one might see in measurements taken among different instruments, samples, and sample preparations.
• “about” refers to ⁇ 20% of a quantity and includes, but is not limited to, ⁇ 15%, ⁇ 10%, and ⁇ 5% of the quantity
• Active agent refers to a compound with a desired pharmacological effect and includes all pharmaceutically acceptable forms of the active agent described
• the active agent can be in an isomeric mixture, a solid complex bound to an ion exchange resin, or the like.
• the active agent can be in a solvated form.
• Active agent also includes all pharmaceutically acceptable salts, derivatives, and analogs of the active agent being described, as well as combinations thereof.
• the pharmaceutically acceptable salts of the active agent may include, without limitation, the sodium, potassium, calcium, magnesium, ammonium, tromethamine, L-lysine, L-arginine, N-ethylglucamine, N-methylglucamine and salt forms thereof, as well as combinations thereof and the like
• Any form of the active agent may be suitable for use in the compositions of the present invention, e.g., a pharmaceutically acceptable salt of the active agent, a free acid or free base of the active agent, or a mixture thereof.
• administering or "administration of a drug to a patient (and grammatical equivalents of this phrase) refers to direct administration, which may be administration to a patient by a medical professional or may be self-administration, and/or indirect administration, which may be the act of prescribing a drug.
• direct administration which may be administration to a patient by a medical professional or may be self-administration
• indirect administration which may be the act of prescribing a drug.
• a physician who instructs a patient to self-administer a drug and/or provides a patient with a prescription for a drug is administering the drug to the patient.
• Advanced solid tumor refers to a solid tumor that has relapsed, progressed, metastasized after, and/or is refractory to, the initial or first line treatment.
• Advanced solid tumors include, but are not limited to, metastatic tumors in bone, brain, liver, lungs, lymph node, pancreas, prostate, and soft tissue (sarcoma) [0022] "Cancer” refers to leukemias, lymphomas, carcinomas, and other malignant tumors of potentially unlimited growth that can expand locally by invasion and systemically by metastasis.
• cancers include, but are not limited to, cancer of the adrenal gland, bone, brain, breast, bronchi, colon and/or rectum, gallbladder, head and neck, kidneys, larynx, liver, lung, neural tissue, pancreas, prostate, parathyroid, skin, stomach, and thyroid
• Certain other examples of cancers include, acute and chronic lymphocytic and granulocytic tumors, adenocarcinoma, adenoma, basal ceil carcinoma, cervical dysplasia and in situ carcinoma, Ewing's sarcoma, epidermoid carcinomas, giant cell tumor, glioblastoma multiforma, hairy-cell tumor, intestinal ganglioneuroma, hyperplastic corneal nerve tumor, islet cell carcinoma, Kaposi's sarcoma, leiomyoma, leukemias, lymphomas, malignant carcinoid, malignant melanomas, malignant hypercalcemia, marfanoid habitus tumor, medullary carcinoma,
• Dosage form refers to physically discrete units suitable as unitary dosages for human subjects and other mammals, each unit containing a predetermined quantity of active agent calculated to produce the desired onset tolerability and therapeutic effects, in association with one or more suitable pharmaceutical excipients such as carriers
• Excipient includes any inert substance combined with an active agent such as TH-302 to prepare a convenient dosage form and vehicle for delivering the active agent
• Formulation and composition are used interchangeably and refer to a mixture of two or more compounds, elements, or molecules In some aspects the terms “formulation” and “composition” may be used to refer to a mixture of one or more active agents with a carrier or other excipients
• a pharmaceutical formulation is suitable for administration to a human or mammal
• Hyperprohferative disease refers to a disease characterized by cellular hyperproliferation (e g , an abnormally increased rate or amount of cellular proliferation), including cancer as well as other diseases, such as those where the hyperproliferation is part of an immune reaction, as occurs in autoimmune disorders
• hyperprohferative diseases other than cancer include, but are not limited to, allergic angitis and granulomatosis (Churg-Strauss disease), asbestosis, asthma, atrophic gastritis, benign prostatic hyperplasia, bullous pemphigoid, coeliac disease, chronic bronchitis and chronic obstructive airway disease, chronic sinusitis, Crohn's disease, demyelinating neuropathies, dermatomyositis, eczema including atopic dermatitis, eustachean tube diseases giant cell arteritis, graft rejection, hypersensitivity pneumonitis, hypersensitivity vasculitis (Henoch-Schonlein
• HAP Hypoxia activated prodrug
• HAPs include prodrugs that are activated by a variety of reducing agents and reducing enzymes, including without limitation single electron transferring enzymes (such as cytochrome P450 reductases) and two electron transferring (or hydride transferring) enzymes
• HAPs are 2-n ⁇ tro ⁇ m ⁇ dazoIe triggered hypoxia-activated prodrugs
• Examples of HAPs include without limitation, TH-302, TH-281 , PR104 and AQ4N Methods of synthesizing TH-302 are described in PCT Pat App Pub Nos WO 07/002931 and WO 08/083101, incorporated herein by reference Methods of synthesizing PR104 are described in US Pat App No 2007/0032455, incorporated herein by reference Other
• “Pharmaceutically acceptable salt” refers to salts of active agents that are prepared with relatively nontoxic acids
• the compound of the present invention contains relatively basic functionalities, and acid addition salts can be obtained by contacting the neutral form of such compounds with a sufficient amount of the desired acid, either neat or in a suitable inert solvent
• pharmaceutically acceptable acid addition salts include those derived from inorganic acids like hydrochloric hydrobromic, nitric, carbonic, monohydrogencarbonic, phosphoric monohydrogenphosphoric, dihydrogen-phospho ⁇ c, sulfuric, monohydrogensulfuric hyd ⁇ odic, or phosphorous acids and the like, as well as the salts derived from relatively nontoxic organic acids like acetic, propionic, isobuty ⁇ c, malonic, benzoic succinic, suberic, fumaric, mandelic, phthahc, benzenesulfonic, p-tolylsulfonic, citric, tartaric, methanes
• Prodrug refers to a compound that, after administration, is metabolized or otherwise converted to a biologically active or more active compound (or drug) with respect to at least one property
• a prodrug, relative to the drug is modified chemically in a manner that renders it, relative to the drug, less active or inactive, but the chemical modification is such that the corresponding drug is generated by metabolic or other biological processes after the prodrug is administered
• a prodrug may have, relative to the active drug, altered metabolic stability or transport characteristics, fewer side effects or lower toxicity, or improved flavor (for example, see the reference Nogrady, 1985, Medicinal Chemistry A Biochemical Approach, Oxford University Press, New York, pages 388-392, incorporated herein by reference).
• a prodrug may be synthesized using reactants other than the corresponding drug.
• QnD or “qnd” refers to drug administration once every n days.
• QD or qd refers to once every day or once daily dosing
• Q2D or q2d refers to a dosing once every two days
• Q7D refers to a dosing once every 7 days or once a week
• Q5D refers to dosing once every 5 days.
• Reduction of a symptom or symptoms refers to decreasing the severity or frequency of the symptom(s), or elimination of the symptom(s).
• Solid tumor refers to a cancer other than leukemia.
• T 1Z2 refers to the "half-life" of a drug; i.e., the amount of time required for the concentration of a drug in, e.g., plasma, serum, or blood, to be halved.
• the t ⁇ 2 of anticancer drugs that are not hypoxically activated are provided for example, in most recent editions of the PHYSICIANS' DESK REFERENCE, Medical Economics Company, Inc., Oradell, N.J.; and Goodman & Gilman's THE PHARMACOLOGICAL BASIS OF THERAPEUTICS", McGraw-Hill, New York and/or are discussed in the medical literature.
• the t 1/2 of hypoxicaliy activated prodrugs can be found in the literature or determined using routine pharmacokinetic analysis methods.
• "Therapeutically effective amount" of a drug refers to an amount of a drug that, when administered to a patient with cancer or other hyperproliferative disease, will have the intended therapeutic effect, e.g., alleviation, amelioration, palliation or elimination of one or more manifestations of cancer or another hyperproliferative disease in the patient.
• a therapeutic effect does not necessarily occur by administration of one dose, and may occur only after administration of a series of doses. Thus, a therapeutically effective amount may be administered in one or more administrations.
• Treating" or “treatment of” a condition or patient refers to taking steps to obtain beneficial or desired results, including clinical results.
• beneficial or desired clinical results include, but are not limited to, alleviation or amelioration of one or more symptoms of cancer or other hyperproliferative disease; diminishment of extent of disease; delay or slowing of disease progression; amelioration, palliation, or stabilization of the disease state; or other beneficial results.
• Treatment of cancer may, in some cases, result in partial response or stable disease.
• a plurality of items, structural elements, compositional elements, and/or materials may be presented in a common list for convenience.
• CT Computed tomography
• TH-302 can be administered to patients in accord with the invention in any pharmaceutically acceptable formulation.
• PCT Publications WO 08/083101 and WO 07/002931 both incorporated herein by reference, disclose methods for preparing liquid pharmaceutical formulations of TH-302 and other compounds of Formula I
• WO 07/002931 discloses that TH-302 can be provided as a lyophilized powder in a vial and reconstituted in saline or 5% dextrose in water (D5W) immediately prior to administration. After reconstitution in D5W, the TH-302 formulation must be used within 8 hours.
• TH-302 can be administered as a liquid formulation in ethanol (containing up to 50 mg of TH-302 per ml)
• these prior art formulations have limitations in that they are not suitable for high concentrations of drug, and the stability (particularly with respect to keeping the active agent from precipitating) during long term storage and/or dilution of TH-302 is suboptimal.
• the present inventors discovered that the poor aqueous solubility of the nitro-heteroaryl phosphoramide class of hypoxia-activated cancer drugs, such as TH- 302, and other compounds of Formula I, can be improved by providing a nonionic surfactant for prolonged storage in an alcohol environment.
• This section describes certain preferred formulations containing ethanol and a nonionic surfactant such as TWEEN 80 ® .
• TWEEN 80 is sorbitan mono-oleate polyoxyethylene, CAS number 9005-65-6.
• these preferred parenterally administrable pharmaceutical compositions provide improved stability and reduced degradation and precipitation for TH-302, as well as for other nitro-heteroaryl phosphoramide class hypoxia-activated cancer drugs with poor solubility, including TH-281 , and other compounds of Formula I.
• these preferred formulations provide for a higher concentration of the active drug, e.g., TH-302, relative to other formulations that have been previously described. Because these liquid formulations are stable over the long term, no lyophilization of the drug is required, which eliminates the need to reconstitute a lyophilisate before use.
• the pharmaceutically acceptable formulation is suitable for parenteral administration.
• the present inventors have developed a concentrated, stable pharmaceutical composition and methods which can improve the stability of a poorly soluble nitro-heteroaryl phosphoramide class of hypoxia-activated cancer drug, such as TH-302 and other compounds of Formula I, by solubilizing and dispersing the drug within the solution for prolonged storage.
• a nonionic surfactant in these formulations is useful for preventing precipitation and degradation of hypoxia-activated cancer drugs, particularly, TH-302 and TH-281 , that may occur upon dilution with an aqueous media before administration.
• a stable TH-302 liquid formulation is provided as a mixture of a nonionic surfactant and a pharmaceutically acceptable alcohol.
• a nonionic surfactant is TWEEN 80.
• Ethanol is preferably included in an amount at least 70% of the mixture by volume. More preferably, the amount of alcohol used is at least about 70% to about 95% by volume, e.g., at least 70%, at least 80%, at least 90%, or at least about 95%.
• the TWEEN 80 or other nonionic surfactant is included in an amount of at least about 5% v/v of the mixture.
• the nonionic surfactant can be included in an amount of about 5 to 10% of the formulation by volume. The nonionic surfactant helps inhibit precipitation of TH-302 out of the solution in the carrier.
• nonionic surfactant may provide various other functions and advantages, such as acting as an antimicrobial or antibacterial agent.
• Other exemplary nontoxic, nonionic surfactants suitable for use in the present invention include, but are not limited to, polysorbates (e.g., polyoxyethylene (20) sorbitan monolaurate, polyoxyethylene (20) sorbitan monopalmitate, polyoxyethylene (20) sorbitan monostearate and polyoxyethylene (20) sorbitan monooleate); alkylated aryl polyether alcohols known as TRITON ® ; polyethylene glycol tertdodecyl throether available as NONIC ® ; fatty and amide condensate or ALROSOL ® ; aromatic polyglycol ether condensate or NEUTRONYX ® ; fatty acid alkanolamine or NINOL ® sorbitan monolaurate or SPAN ® ; polyoxyethylene sorbitan esters or TWEENs
• polysorbates
• the liquid compositions of the present invention comprise from about 10 mg/ml to about 300 mg/ml of the active agent.
• concentrations can be adjusted depending upon the particular active agent utilized and the amount of active agent desired in the final formulation.
• the amount of TH-302 included in the present liquid formulation is dictated by the intended use.
• the concentration of TH-302 will be in the range of 10 mg/ml to about 300 mg/ml or 30 mg/ml to about 300 mg/ml, more typically 50 mg/ml to 200 mg/ml, more usually 50 mg/ml to about 150 mg/ml, and even more usually 50 mg/ml to 125 mg/ml, and most usually greater than 50 mg/ml, such as about 60 mg/ml, 60 mg/ml to 100 mg/ml, 100 mg/ml to 150 mg/ml, 100 mg/ml to 200 mg/ml, or 100 mg/ml to about 300 mg/ml.
• the carrier is ethanol
• the pharmaceutical formulation includes at least 5% v/v TWEEN 80.
• the formulation comprises about 5 to 10% (v/v) TWEEN 80, 90-95% (v/v) ethanol, and about 50 mg/ml to 125 mg/ml TH-302, such as about 60 mg/ml TH-302.
• the formulation comprises about 5% TWEEN 80, about 95% ethanol, and about 60 mg/ml TH-302.
• the active agent in the formulation is TH-302, including all pharmacologically acceptable forms.
• the invention provides a liquid composition, wherein the active agent is TH-302 in its non-salt form.
• the active agent is TH-281, optionally in its non-salt form, or another compound of Formula I.
• the active agent can be provided for dissolution into the formulation of the invention in any suitable form.
• it can be in the form of a powder, pellet, or a granule (i.e., an aggregate of smaller units of active agent). Any pharmaceutical grade of TH-302 or other compound of Formula I may be used.
• the present formulation comprising a nonionic surfactant provides a long-term stability characterized by TH-302 degradation of 15% or less over a period of 31 days or less at about -2O 0 C to about 25 0 C.
• a formulation comprising a nonionic surfactant e.g., TWEEN 80
• TWEEN 80 provides a long-term stability characterized by TH-302 degradation of 5% or less over a period of 31 days or less at about -2O 0 C.
• the TH-302 liquid formulation produced according to the present invention exhibits superior stability, where stability, in this instance, is characterized by TH-302 remaining in solution, e.g., not precipitating during storage or upon thawing.
• the formulation may optionally further comprise other components described herein.
• mixtures of carriers are used.
• a second carrier in addition to ethanol
• it is generally N,N-dimethylacetamide (DMA).
• DMA N,N-dimethylacetamide
• the amide carrier is preferably included in an amount up to about 20% of the formulation by volume. Preferably the amount of amide carrier used is about 10% to about 20% by volume.
• the formulation consists of ethanol and TH-302. In some embodiments the formulation consists of ethanol, DMA and TH-302.
• compositions of the present invention can additionally include an antioxidant, preserving agents such as methyl-, ethyl-, and propyl-hydroxy- benzoates, butylated hydroxytoluene, and butylated hydroxyanisole; opacifying agents and chelating agents.
• Suitable antioxidants and chelating agents include for example, butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), propyl gallate (PG), ascorbyl palmitate, disodium EDTA (ethylenediamine tetraacetic acid; also known as disodium edentate), EDTA, tartaric acid, citric acid, citric acid monohydrate, and sodium sulfite.
• the foregoing compounds are included in the pharmaceutical formulations in amounts in the range of about 0.01% to about 5% w/w.
• the pharmaceutical formulation includes BHA, BHT, or PG used at a range of about 0.02% to about 1% and disodium EDTA, citric acid, or citric acid monohydrate used at a range of about 2% to about 5%.
• the pharmaceutical formulation includes BHA used at about 0.05% w/w.
• any suitable method can be used to mix the formulation comprising the active agent, alcohol carrier, and non-ionic surfactant.
• the active agent, alcohol carrier, and non-ionic surfactant are combined, and the mixture is administered directly to the patient, optionally after dilution.
• liquid pharmaceutical formulations of the invention can be conveniently provided in dosage forms. Methods for preparing dosage forms of other liquid formulations are known, and it will be apparent to those skilled in the art upon consideration of the instant disclosure how to prepare suitable dosage forms of the pharmaceutical formulations of the invention.
• a liquid dosage form of the present invention can be prepared according to the procedures set forth, for example, in Remington: The Science and Practice of Pharmacy, 20* n Ed., Lippincott, Williams & Wilkins (2003), and similar publications.
• the dosage form to be administered will, in any event, contain a quantity of the active agent in a therapeutically effective amount for relief of the condition being treated when administered in accordance with the teachings of this invention.
• the pharmaceutical formulations of the invention can be packaged in any packaging that facilitates stability of the drug formulation.
• the pharmaceutical formulations provided by this invention may be contained in a sterilized vessel such as syringes, vials, or ampoules of various sizes and capacities.
• the sterilized vessel may optionally contain between 1-50 ml, 1-25 ml, 1-20 ml, 1-10 ml or 1-5 ml of the formulations.
• Sterilized vessels maintain sterility of the pharmaceutical formulations, facilitate transportation and storage, and allow administration of the pharmaceutical formulations without prior sterilization step.
• the present invention also provides a kit for administering the liquid formulation comprising the active agent to a host in need thereof.
• the kit comprises the active agent (e.g., TH-302) and a carrier (e.g., ethanol), comprising the nonionic surfactant (e.g., TWEEN 80).
• the active agent e.g., TH-302
• a carrier e.g., ethanol
• the nonionic surfactant e.g., TWEEN 80
• the kit may comprise a first vessel comprising a hypoxia-activated cancer drug in a solid form; and a vessel comprising a carrier that contains a nonionic surfactant; wherein adding the carrier to the solid drug results in the formation of a pharmaceutical formulation for administering the drug.
• Mixing the solid drug and carrier may optionally form a pharmaceutical formulation that comprises TH-302 in a concentration described above, e.g., about 60 mg/ml.
• a pharmaceutical formulation that comprises TH-302 in a concentration described above, e.g., about 60 mg/ml.
• TH-302 in a concentration described above, e.g., about 60 mg/ml.
• TH-302 per ml of the carrier, optionally between 50 and 200 mg, and between 100 mg and 150 mg per ml of the carrier and nonionic surfactant may be used.
• the pharmaceutical formulations provided in vessels or kits may be in a form that is suitable for direct administration or may be in a concentrated form that requires dilution relative to what is administered to the patient.
• pharmaceutical formulations, described in this invention may be in a form that is suitable for direct administration via intravenous administration or may be in a concentrated form that is diluted prior to administration.
• about 500 to 1200 mg of TH-302 in a formulation of the invention is administered to a patient over 30-60 minutes after dilution in D5W to about 500 ml total volume.
• the compositions of the present invention are useful in therapeutic applications, e.g., for treating cancer.
• a hypoxia-activated cancer drug formulation is infused through a connector, such as a Y site connector, that has three arms, each connected to a tube.
• a connector such as a Y site connector
• BAXTER ® Y-connectors of various sizes can be used.
• a vessel containing hypoxia-activated cancer drug formulation is attached to a tube further attached to one arm of the connector.
• Infusion fluids such as 0.9% sodium chloride, or 5% dextrose, or 5% glucose, or Lactated Ringer's, are infused through a tube attached to the other arm of the Y-site connector.
• the infusion fluids and hypoxia-activated cancer drug formulations are mixed inside the Y site connector.
• the resulting mixture is infused into the patient through a tube connected to the third arm of the Y site connector.
• the advantage of this administration approach over the prior art is that the hypoxia-activated cancer drug is mixed with infusion fluids before it enters the patient's body, thus reducing the time when decomposition of therapeutic formulations may occur due to contact with water.
• the hypoxia-activated cancer drug is mixed less than 10, 5, 2 or 1 minutes before entering the patient's body.
• the hypoxia- activated cancer drug is mixed less than 8, 6, 4, 2 or 1 hours before entering the patient's body.
• pharmaceutical formulations according to the present invention provide the further advantage because the nonionic surfactant/alcohol solution can be readily mixed with water, D5W or saline, the formulations can be easily and readily further diluted just prior to administration.
• the pharmaceutical formulations can be diluted with water, saline or D5W within the 8 hour period preceding administration to a patient.
• the infusion administration is performed after determining the mg dose for a patient by multiplying the patient's body surface area by the prescribed TH-302 dose.
• the appropriate number of vials (for example, 100 mg/vial) of TH-302 are removed from a -2O 0 C freezer and left in an ambient room condition for 30-60 minutes to allow vials to warm to room temperature.
• Each 100 mg vial is reconstituted with 25 ml sterile D5W and shaken well.
• the number of ml of reconstituted TH-302 required is calculated by multiplying the desired mg dose by 0.25 (e.g., a 1000 mg dose requires 250 ml).
• TH-302 Prior to adding reconstituted TH-302 to a 500/1000 ml sterile D5VV IV bag, the equivalent volume of TH-302 to be added to the bag is removed, so that when the reconstituted drug is added to the bag the total volume is 500/1000 ml.
• Patients may be infused with hypoxia-activated cancer drug formulations for any therapeutically suitable time, e.g., about 15, 30, or 45 minutes or for 1, 2, 3, 4, 5 or more hours.
• the speed and volume of the infusion can be regulated according to the patient's needs.
• the regulation of the infusion of hypoxia-activated cancer drug formulations can be performed according to existing protocols. For illustration, Table 1 outlines exemplary dilution volumes and infusion times based on total dose administered for TH-302 (longer infusion times are permitted based on physician judgment of the time required to administer the infusion volume).
• an individual patient's surface area can be determined using routine methods known to oncologists and other medical providers.
• the pharmaceutical formulations of the invention may be co-administered with other agents. Co-administration in the context of this invention is defined to mean the administration of more than one therapeutic agent in the course of a coordinated treatment to achieve an improved clinical outcome.
• the additional agent administered may be in any conventional form and may include infusion fluids, therapeutic compounds, nutritious fluids, anti-microbial fluids, buffering and stabilizing agents.
• Therapeutic compounds include, but are not limited to, anti-neoplastic agents, alkylating agents, agents that are members of the retinoids superfamily, antibiotic agents, hormonal agents, plant-derived agents, biologic agents, interleukins, interferons, cytokines, immuno-modulating agents, and monoclonal antibodies.
• the additional agent is an anti-neoplastic drug in preferred embodiments administration of the two agents is non-contemporaneous.
• the TH-302 formulations of the present invention may be administered, or co-administered with a non-hypoxia activated anticancer agent, via local delivery. See Sections III - V, infra, and Examples.
• the formulation, dose, administration route, frequency, and such other modes of administration of various anticancer agents other than TH-302, such as docetaxel, doxorubicin, gemcitabine, and pemetrexed, administered in accordance with the present methods, are disclosed herein, available in medical literature, and/or known to one of skill in the art.
• Local delivery of the pharmaceutical formulations of this invention can be by a variety of techniques and structures that administer the pharmaceutical formulation at or near a desired site. Examples of local delivery techniques and structures are not intended to be limiting but rather as illustrative of the techniques and structures available. Examples include local delivery catheters, site-specific carriers, implants, direct injection, or direct applications.
• Local delivery by a catheter allows the administration of a sequential combination of therapeutic agents and/or compositions directly to the desired site according to the methods of the invention.
• Examples of local delivery using a balloon catheter are described in EP 383 492 A2 and U.S. Pat. No. 4,636,195. Additional examples of local, catheter-based techniques and structures are disclosed in U.S. Pat. No. 5,049,132 and U.S. Pat. No. 5,286,254.
• the catheter is placed such that the therapeutic agents can be delivered at or near the desired site. Dosages delivered through the catheter can vary, according to determinations made by one of skill, but often are in amounts effective to create a cytotoxic or cytostatic effect at the desired site.
• these total amounts are less than the total amounts for systemic administration of the pharmaceuticals of this invention, and are less than the maximum tolerated dose.
• Delivery of the pharmaceutical formulations of this invention through catheters preferably should be formulated to a viscosity that enables delivery through a small treatment catheter, and may be formulated with pharmaceutically acceptable additional ingredients (active and inactive).
• Additional ingredients active and inactive.
• Local delivery by an implant describes the placement of a matrix that contains the pharmaceutical formulations of this invention into the desired site. The implant may be deposited by surgery or other means. The implanted matrix releases the inventive combination of therapeutic agents and/or compositions by diffusion, chemical reaction, solvent activators, or other equivalent mechanisms. Examples are set forth in Langer, 1990, Science 249:1527-33.
• the implants may be in a form that releases the inventive combination of therapeutic agents and/or compositions over time; these implants are termed time-release implants.
• the material of construction for the implants will vary according to the nature of the implant and the specific use to which it will be put.
• bio-stable implants may have a rigid or semi-rigid support structure, with inventive combination of therapeutic agents and/or composition delivery taking place through a coating or a porous support structure.
• Other implants may be made of a liquid that stiffens after being implanted or may be made of a gel.
• the amounts of inventive combination of therapeutic agents and/or composition present in or on the implant may be in an amount effective to treat cell proliferation generally, or a specific proliferation indication, such as the indications discussed herein.
• the formulations of the present invention can be used to treat any type of cancer in a subject, particularly cancers containing substantial areas of hypoxic tissue.
• cancers include but are not limited to lung cancer (including small cell lung cancer and non-small cell lung cancer), breast cancer, colon cancer, head and neck cancer, ovarian cancer, pancreatic cancer, soft tissue sarcomas, and prostate cancer.
• the formulations of the invention can also be used to treat non-cancer hyperproliferative diseases
• TH-302 formulated as discussed above may be administered as monotherapy or in combination with administration of another anticancer agent(s).
• the formulation may be administered in conjunction with a therapeutic cancer treatment, including but not limited to surgery (e.g., in an adjuvant or neoadjuvant setting) or radiation.
• TH-302 can be administered as monotherapy, / ' e , alone, not in combination with any other anticancer agent, to treat cancer.
• TH-302 is administered as a monotherapy for the treatment of melanoma (including metastatic melanoma) or SCLC (including refractory SCLC)
• melanoma including metastatic melanoma
• SCLC including refractory SCLC
• TH-302 is usually administered intravenously (e g., by infusion) for monotherapy.
• a TH-302/ethanol/TWEEN 80 formulation discussed supra is diluted into D5W or saline for infusion.
• typically TH-302 is administered for one or more cycles of (a) once weekly for 3 consecutive weeks followed by a week of no TH-302 administration (e g , administered on days 1 , 8, and 15 of a 28 day cycle) referred to as a "4 week cycle", (b) once per week; (c) once every three weeks, or (d) twice every three weeks (e.g., administered on days 1 and 8 of a 21 -day cycle).
• TH-302 can be administered, for example, at a dose of 480 mg/m 2 to 670 mg/m 2 , most preferably 480 mg/m 2 to 575 mg/m 2 , preferably about 575 mg/m 2
• TH-302 can be administered once weekly at doses up to 575 mg/m 2 .
• the dose can be up to 670 mg/m 2 .
• doses up to 940 mg/m 2 or higher can be administered once every 3 weeks. Other doses may be selected based on the patient's age, health and other factors.
• the amount of TH-302 administered is about 670 mg/m 2 , 575 mg/m 2 , 560 mg/m 2 , 480 mg/m 2 , 360 mg/m 2 , 240 mg/m 2 , and 120 mg/m 2 , when the TH-302 is administered intravenously (e g , by infusion)
• TH-302 is usually administered in multiple cycles.
• TH-302 may be administered using a "4 week cycle" for from 1 to 13 cycles, from 1 to 7 cycles, or from 1 to 4 cycles.
• TH-302 may be administered at a frequency of once every week for 3 to 52, 3 to 28, 3 to 6, or 3 to 8 cycles (weeks)
• TH-302 may be administered at a frequency of once every three weeks for 3 to 52, 3 to 28, 3 to 6, or 3 to 8 weeks. It will be recognized by medical professionals that certain of these periods of TH-302 administration include one or more weeks of drug holidays during which no TH-302 is administered
• TH-302 has shown benefit in patients with metastatic melanoma
• the historical response rate in first-line metastatic melanoma is about 10%, so the results of treatment with TH-302 are quite remarkable.
• Eleven subjects with metastatic melanoma have been treated with TH-302 monotherapy at initial doses of 575 mg/m 2 to 670 mg/m 2 as part of a 3 consecutive week dosing regimen repeated every 4 weeks.
• RECIST tumor assessments have been performed for eight subjects. Three of the eight subjects assessed have had partial responses and three of eight subjects have had stable disease. Four of the eight subjects continued on-study for additional dosing cycles. Two of the three subjects with a partial response continued on-study through at least Cycle 3 and Cycle 7.
• the therapeutically effective dose of TH-302 in the methods of treating cancer is in an amount in the range of about 100 mg/m 2 - about 700 mg/m 2 , 200 mg/m 2 - about 700 mg/m 2 , about 300 mg/m 2 - about 600 mg/m 2 , about 350 mg/m 2 - about 550 mg/m 2 , about 400 mg/m 2 - about 500 mg/m 2 , about 400 mg/m 2 - about 600 mg/m 2 , about 450 mg/m 2 - about 550 mg/m 2 , about 450 mg/m 2 - about 575 mg/m 2 , about 480 mg/m 2 - about 670 mg/m 2 , and about 670 mg/m 2 - ⁇ 940 mg/m 2 .
• the present invention provides methods of treating cancer comprising administering TH-302 in an amount in the range of about 700 mg/m 2 - about 1200 mg/m 2 or about 800 mg/m 2 - about 1000 mg/m 2 , particularly when prophylaxis against toxicity is provided, for example as discussed below.
• the therapeutically effective dose of TH-302 for monotherapy is about 200 mg/m 2 - about 500 mg/m 2 .
• the invention provides administering TH-302 monotherapy to a patient with small cell lung cancer.
• the TH-302 is administered once per week for 3 weeks followed by one week with no administration (e.g., days 1, 8 and 15 of a 28-day cycle).
• the TH-302 is administered to a patient with small cell lung cancer once per week for 3 weeks followed by one week with no administration at a dose in the range of about 480 mg/m 2 - about 670 mg/m 2 .
• the TH-302 is administered for at least 2, at least 3, at least 4, at least 5, or at least 6 28-day cycles.
• the TH-302 is administered once every three weeks (e.g., day 1 of a 21 -day cycle). In some embodiments the TH-302 is administered to a patient with small cell lung cancer once every 3 weeks at a dose in the range of about 670 mg/m 2 - less than 940 mg/m 2 . In some embodiments the TH-302 is administered for at least 2, at least 3, at least 4, at least 5, or at least 6 21 -day cycles. [0082] In one aspect, the invention provides administering TH-302 monotherapy to a patient with metastatic melanoma.
• the TH-302 is administered once per week for 3 weeks followed by one week with no administration (e.g., days 1 , 8 and 15 of a 28-day cycle). In some embodiments the TH-302 is administered at a dose in the range of about 480 mg/m 2 - about 670 mg/m 2 , sometimes about 575 mg/m 2 - about 670 mg/m 2 . In some embodiments the TH-302 is administered for at least 2, at least 3, at least 4, at least 5, or at least 6, 28-day cycles.
• TH-302 has an attractive safety profile as monotherapy. It is well tolerated at relatively high doses and does not induce significant dose limiting myelosuppression.
• the dose limiting toxicities in a dose escalation study were mucositis with one grade 3 event involving the oral mucosa and one grade 3 event involving the gastrointestinal mucosa.
• TH-302 also produces a predictable skin rash that is dose proportional and reversible. The rash is typically grade 1 or grade 2 depending on the dose and increased in incidence starting at a weekly monotherapy dose of 480 mg/m 2 .
• the present invention provides methods for treating cancer in which the patient is administered TH-302 (or another compound of Formula I) in combination with an oral and/or topical formulation of a drug or other agent to prevent mucosal and/or skin damage.
• the drug or agent is administered prophylactically (prior to development of significant mucosal or skin damage).
• suitable topical agents include one or a combination of the following: topical agents containing zinc oxide, anti-fungal agents, anti-oxidants and/or anti-bacterial agents.
• Topical anti-oxidants available for use in humans include topical vitamin C, topical vitamin E, topical melatonin and combinations thereof (see Dreher and Maiback, 2001 , “Protective Effects of Topical Antioxidants in Humans” Oxidants and Antioxidants in Cutaneous Biology. Current Problems in Dermatology. Basel, Karger 29:157-164).
• Topical DMSO may be used (see US Patent 6,060,083, incorporated herein by reference).
• Other agents include, for example, vitamin K analogs (see Pat. Pub.
• topical Vitamin C topical Vitamin E topical corticosteroids, menthol cream, topical minocycline; lotions such as clindamycin 2% /hydrocortisone 1 %, glutamine solutions and melatonin.
• Systemic agents including anti-fungal agents (e.g., nystatin) and anti-bacterial agents (e.g., tetracycline) may be used.
• anti-fungal agents e.g., nystatin
• anti-bacterial agents e.g., tetracycline
• the present invention also provides methods for treating cancer by administering hypoxia activated prodrugs, including TH-302, to cancer patients, in combination with another anticancer drug, wherein the therapeutic efficacy of the combination treatment is maximized and the toxicity of the combination treatment minimized by administering the hypoxia activated prodrug ("HAP") and the other anticancer drug non-contemporaneously.
• HAP hypoxia activated prodrug
• Example 3 infra.
• Administering two drugs a certain time period apart in accordance with the present invention is referred to as “non-contemporaneous administration" of the two drugs.
• Administering two drugs together or one immediately after the other is referred to as “contemporaneous administration" of the two drugs.
• the present invention provides a method of treating cancer by administering two anticancer drugs, a hypoxia activated prodrug and an anticancer drug that is not hypoxically activated, to a patient in need of such treatment, wherein the non-HAP anticancer drug is administered at least about 30 minutes after the immediate prior administration of the hypoxia activated prodrug is stopped.
• the second drug is administered 30 minutes to 8 hours after administration of the HAP drug has stopped.
• the second drug is administered 1 to 6 hours after administration of the HAP drug has stopped (e.g., about 2 hours, about 3 hours or about 4 hours after administration of the HAP drug).
• the duration of the time between administration of TH-302 and the non-HAP drug is from 1 to 10 hours, from 2 to 6 hours, or from 3 to 5 hours.
• the non- HAP anticancer drug is administered 1 hour or longer (e.g., 1, 2, 4, or 6 hours) after administration of the HAP has stopped.
• at least a 2 hour delay is employed.
• the time of administration of the non-HAP drug is at least 30 minutes to one hour, typically at least 2 hours, sometimes at least 4 hours, and in any event no more than 24 hours after administration of the HAP.
• the delay between completion of the administration of the HAP and administration of the second agent is shorter than 8 hours; for example, the delay may be less than 6, less than 6, or less than 4, hours.
• the present invention provides a method for treating cancer in a patient comprising administering a hypoxia activated prodrug in combination with another anticancer drug in which the HAP is administered first, and the delay between completing the administration of the HAP and beginning administration of the other anticancer drug is equal to about the t 1/2 of the HAP, or equal to at least the ti /2 of the HAP, or equal to about twice the t 1/2 of the HAP, or equal to at least twice the t V2 of the HAP.
• the delay is in the range bounded by the ti /2 of the HAP and twice the t-,/ 2 of the HAP.
• the HAP is TH-302, TH-281 , or another compound of Formula I.
• the hypoxia activated prodrug is AQ4N.
• the HAP is PR104 having a structure of formula shown below:
• PR104 is a HAP for which the maximum tolerated dose (MTD) and recommended dose was determined, after a Phase I study, to be 1 ,100 mg/m 2 .
• MTD maximum tolerated dose
• Phase I studies with PR104 were initiated by administering PR104 at 200-275 mg/m 2 . See, Tchekmedyian et al., J Clin Oncol 26: 2008 (May 20 suppl.; abstr. 3575; incorporated herein by reference).
• the MTD of PR104 plus gemcitabine or docetaxel was 140 mg/m 2 for PR104 plus gemcitabine and ⁇ 200 mg/m 2 for PR104 plus docetaxel.
• the methods of the present invention allow higher doses of HAPs to be administered in such combination therapies, including HAPs such as TH-302, TH-281 , PR104, and AQ4N (see for example, PCT Pat. Pub. Nos. WO 00/064864, WO 04/087075, WO 07/002931 , and WO 08/083101, and US Pat. App. Pub. No. 2007/0032455, each of which is incorporated herein by reference).
• the hypoxia activated prodrug is selected from the group consisting of the N-oxides of the vinca alkaloids.
• Certain N-oxides of the vinca alkaloids useful in the methods of the present invention are provided in the PCT patent publication No WO 07/098091 , incorporated herein by reference
• the HAP is a compound described in any of PCT publication Nos WO 2000/064864, 2004/087075, 2005/086951 , 2005/087075, 2006/057946, 2007/002931 2008/083101 , 2008/151253, 2009/018163, and 2009/033165, PCT application No US09/044038 US patent application publication Nos 20050256191 and 20070032455, and US provisional patent application No 61/218,043, each of which is incorporated herein by reference Routes, frequency, and such other parameters of administering therapeutically effective amounts of HAPs are described in these publications as well (see also Jameson et al , J CIm
• Cancer therapy typically involves multiple cycles of drug administration, and for many cancers, multiple drugs are administered
• multiple drugs are administered
• two anticancer drugs, A and B may be administered in various administration sequences, as illustrated below i ABAAABAAABAA (repeats or "cycles" of ABAA) ,
• Ii ABAABAABAABA (cycles of ABA), iii. ABABABABABABABAB (cycles of AB); iv. ABBABBABBABBABB (cycles of ABB); and v. ABBBABBBABBBABBB (cycles of ABBB).
• any of these (and other) cycles of administration can be employed in accordance with the present methods.
• the sequence ABAAABAAABAA can represent 3 cycles in which "A" is TH-302 administered on Days 1, 8 and 15 of a 28 day cycle, and "B" is gemdtabine administered non-contemporaneously with A on Day 1 of the cycle.
• the delay between completing administration of HAP and initiation of administration of the non-HAP drug refers to the period between sequential administrations of HAP and non-HAP.
• Hyperproliferative diseases other than cancer may also be treated using the methods of the invention.
• the anticancer drug that is not hypoxically activated is selected from the group consisting of platinum alkylators (cisplatin, carboplatin, oxaliplatin, and satraplatin), docetaxel, doxorubicin, gemcitabine, paclitaxel, 5- fluorouracil, and pemetrexed.
• the anticancer drugs administered in accordance with the present invention can be administered via a variety of routes, including, without limitation IV and oral routes.
• Routes, frequency, and therapeutically effective amounts of administering anticancer drugs that are not hypoxia activated are provided, for example, in most recent editions of the PHYSICIANS' DESK REFERENCE, Medical Economics Company, Inc., Oradell, N.J.; and Goodman & Gilman's "THE PHARMACOLOGICAL BASIS OF THERAPEUTICS", McGraw-Hill, New York, Brown et al., Cancer Lett, 1978, 5::291-97 (incorporated herein by reference), Yamada et al., Cancer Lett, 2001 , 172:17-25 (incorporated herein by reference), and/or are available from the Federal Drug Administration and/or are discussed in the medical literature.
• the present invention provides a method of treating cancer and other hyperproliferative diseases, said method comprising administering a hypoxia activated prodrug and radiation therapy, to a patient in need of such treatment, wherein the HAP ⁇ e.g., TH-302) is administered from about 1 hour to about 48 hours, more typically about 1 to 24 hours before the radiation therapy is started.
• HAP treatment and radiation treatment both are administered within a 24 hour period, the HAP is administered first, and the radiation is administered at least about 30 minutes and no more than 24 hours after administration of the HAP is stopped.
• the lag between administration of the HAP and radiation treatment is 2-4 hours, such as about 2 hours or about 4 hours.
• the present invention provides methods of treating cancer by administering TH-302 in combination with a second anticancer agent (other than a HAP) to a patient in need of such treatment.
• TH-302 As is discussed below, a wide variety of solid tumors and advanced solid tumors can be treated using such combination therapy, and a wide variety of anticancer agents can be administered in combination with TH-302 for therapeutic benefit.
• clinical data show that the combination of TH-302 with gemcitabine has remarkable activity in first-line pancreatic cancer and the combinations of TH-302 with docetaxel or pemetrexed have remarkable activity in refractory non-small cell lung cancer (NSCLC).
• NSCLC non-small cell lung cancer
• the combination of TH-302 with doxorubicin is very promising in soft tissue sarcoma.
• Anticancer agents which may be used in combination with TH-302, are well know.
• the anticancer agent other than TH-302 is selected from the group consisting of docetaxel, doxorubicin, gemcitabine, and pemetrexed. See Tables 2 and 3, infra.
• the anticancer agent other than TH-302 is selected from the group consisting of platinum alkylators (dsplatin, carboplatin, oxaliplatin, and satraplatin), docetaxel, doxorubicin, gemcitabine, paclitaxel, 5-fluorouracil, and pemetrexed.
• TH-302 can be broadly combined with commonly used standard chemotherapies particularly including gemcitabine, docetaxel, pemetrexed, and doxorubicin.
• the MTD of TH-302 in each of the combinations will likely be greater than 50% of the MTD of weekly TH-302 monotherapy.
• Broad activity has been observed with RECIST responses in all four of the combinations of TH-302 with gemcitabine, docetaxel, pemetrexed, and doxorubicin. Partial responses were observed at all TH-302 dose levels including at the lowest dose of TH-302 (240 mg/m 2 ) studied in the combinations.
• the response rates are considerably higher than one would expect based on prior studies in similar trials or in similar trials of specific tumors such as pancreatic cancer, recurrent NSCLC, and soft-tissue sarcoma.
• many of the responses are durable, thus providing well-defined clinical benefit for the subjects.
• the proportion of subjects with stable disease on treatment is also notable and the measure of clinical benefit described by the sum of partial responses (28%) and stable disease (51%) is nearly 80%.
• TH-302 when administered as part of a combination treatment for cancer, TH-302 is typically administered in amounts lesser than those administered in TH-302 monotherapy.
• administration of TH-302 and a second chemotherapeutic agent is conducted in accord with the methods described in Section IV, supra. That is, the drugs are administered non-contemporaneously, with the administration of the non-HAP beginning after administration of the TH-302.
• administration of the non-HAP commences 30 min to 6 hours after completion of TH-302 administration (e.g., a delay of about 1, about 2, about 3, about 4, about 5, or about 6 hours). In some embodiments administration of the non-HAP commences about 2 hours after completion of TH-302 administration.
• TH- 302 is usually administered by IV infusion at a dose of 200 mg/m 2 - 500 mg/m 2 .
• TH-302 when administered in combination with another anticancer agent, is administered in an amount of about 120 mg/m 2 , 240 mg/m 2 , 340 mg/m 2 , 400 mg/m 2 , 480 mg/m 2 , and 560 mg/m 2 .
• the dose will depend, in part, on what chemotherapeutic agent other than TH-302 is used, as well as the patient's condition and cancer being treated.
• the MTD of TH-302 plus gemcitabine is anticipated to be 340-400 mg/m 2 ; the MTD of TH-302 plus docetaxel is 340 mg/m 2 , and the MTD of TH-302 plus pemetrexed is 480 mg/m 2 ; and the MTD of TH-302 plus doxorubicin is anticipated to be 300 mg/m 2 ; in each case when the non-HAP drug is non-contemporaneously administered at conventional doses, e.g., as described below.
• TH-302 may be administered in combination with another agent in an amount in the range of about 100 mg/m 2 - about 700 mg/m 2 , about 300 mg/m 2 - about 600 mg/m 2 , about 350 mg/m 2 - about 550 mg/m 2 , about 400 mg/m 2 - about 500 mg/m 2 , about 400 mg/m 2 - about 600 mg/m 2 , about 450 mg/m 2 - about 550 mg/m 2 , about 200 mg/m 2 - about 500 mg/m 2 , or about 200 mg/m 2 - 575 mg/m 2 .
• TH-302 may be administered according to a variety of schedules, including those described is administered for one or more 4 week cycles, as described above for TH-302 monotherapy (i.e., once per week for three weeks followed by one week without administering TH-302).
• TH-302 is administered for one or more 3 week cycles.
• TH- 302 can be administered once weekly for 2 consecutive weeks followed by a week of no TH-302 or, alternatively, can be administered once every 3 weeks.
• TH-302 is administered weekly.
• TH-302 may be administered once weekly for seven weeks followed by one week of no administration, followed by one or more 28-day cycles.
• TH-302 is usually administered intravenously, typically by infusion.
• TH-302 is formulated with ethanol and TWEEN 80 as discussed in Section II, supra (discussing administration of TH-302 for monotherapy).
• TH-302 is administered prior to administration of the second, non-HAP anticancer agent, and administration of TH-302 is stopped at least 30 minutes to one hour (or at least 2-6 hours) before administration of the second, non-HAP anticancer agent is initiated, i.e., as described in Section III, supra.
• the present invention provides methods of treating cancer comprising administering TH- 302 intravenously, in combination with another anticancer agent to a patient in need of such treatment, where the TH-302 is administered in an amount of up to about 1000 mg/m 2 .
• the dose of TH-302 used in a particular combination therapy and administration schedule is in the range bounded by the MTD for the particular schedule and combination and a dose equal to the MTD minus 100 mg/m 2 (i.e., in some embodiments the dose of TH-302 used in a particular combination therapy and administration schedule is dosed up to 100 mg/m 2 less than the MTD).
• TH-302 may be administered in combination with one (or more) additional chemotherapeutic agents as an initial or first line treatment, for treatment of refractory or metastatic cancer, and as adjuvant or neoadjuvant therapy.
• additional chemotherapeutic agents as an initial or first line treatment, for treatment of refractory or metastatic cancer, and as adjuvant or neoadjuvant therapy.
• the cancer is treated, following diagnosis, in the neoadjuvant setting (chemotherapy is administered to the patient before surgery to shrink the primary tumor and facilitate removal of the primary tumor).
• the combination therapy is administered, following diagnosis, as adjuvant treatment (chemotherapy is given after the tumor is removed and the patient is staged; if there is a high likelihood of recurrent then prophylactic chemotherapy is given to delay recurrence and improve survival).
• the combination therapy is administered for treatment of refractory or metastatic cancer (chemotherapy is given for recurrence(s) or spread of the cancer).
• Treatable cancers in accordance with the methods herein include, therefore, previously untreated cancers, a refractory cancer, and a metastatic cancer.
• the relapsed cancer, refractory cancer, or metastatic cancer treated is selected from the group consisting of lung cancer, liver cancer, prostate cancer and skin cancer.
• NSCLC NSCLC
• prostate cancer neuroendocrine cancer
• anal cancer urachal cancer, urethral cancer
• breast cancer melanoma
• renal cell carcinoma with TH- 302 and docetaxel
• esophageal cancer pancreatic cancer, NSCLC, neuroendocrine cancer, soft tissue sarcoma, colorectal cancer, hepatocellular carcinoma (HCC), renal cancer, and parotid cancer with TH-302 and pemetrexed.
• TH-302 is administered in combination with docetaxel, the cancer treated is prostate cancer, and TH-302 is administered in an amount in the range of about 200 mg/m 2 - 500 mg/m 2 , usually about 340 mg/m 2 .
• TH-302 is administered in combination with doxorubicin, the cancer treated is soft tissue sarcoma, and TH-302 is administered in an amount in the range of about 200 mg/m 2
• TH-302 is administered in combination with pemetrexed, the cancer treated is non small cell lung cancer (NSCLC), and TH-302 is administered in an amount in the range of about 200 mg/m 2 - 500 mg/m 2 , usually about 400 mg/m 2 .
• NSCLC non small cell lung cancer
• TH-302 is administered in combination with gemcitabine, the cancer treated is pancreatic cancer, and TH-302 is administered in an amount in the range of about 200 mg/m 2 - 500 mg/m 2 , usually about 340 - 400 mg/m 2 .
• TH-302 (or other compound of Formula I) can be administered at frequencies and durations described for TH-302 monotherapy above
• the TH-302 is administered at a frequency of once every week
• TH 302 is administered in multiple cycles, each cycle of administration being a 4 week cycle wherein, TH-302 is administered once weekly for 3 consecutive weeks
• TH-302 administered once weekly for 3 consecutive weeks is administered on days 1, 8, and 15, followed by a week of no drug administration, followed by a week of no TH-302 administration.
• the TH-302 is administered for a period in the range of 3 weeks - 52 weeks, 3 weeks - 28 weeks, 3 weeks - 16 weeks, and 3 weeks
• TH-302 can be administered, for example and without limitation, for 1-13, 1-7, or 1-4 cycles Certain of these periods of TH-302 administration include one or more weeks of drug holidays during which no TH-302 is administered.
• the doses of the non-TH- 302 chemotherapeutic agent are approved doses listed in their respective product labeling
• the therapeutically effective amount of an anticancer agent other than TH- 302 administered in accordance with the present methods are known to physicians and are provided, for example and without limitation, in the product descriptions found in the PHYSICIANS' DESK REFERENCE, 2003, 57th Ed., Medical Economics Company, Inc., Oradell, N.J; Goodman & Gilman's THE PHARMACOLOGICAL BASIS OF THERAPEUTICS" 2001 , 10 th Edition, McGraw-Hill, New York; and/or are available from the Federal Drug Administration and/or are discussed in the medical literature.
• Illustrative dosing amounts and schedules for various cancers in accordance with the methods of the invention are described herein.
• Gemcitabine may be administered IV at 1 ,000 mg/m 2 IV over 30 minutes.
• gemcitabine may be administered IV at 1 ,000 mg/m 2 IV over 30 minutes on Days 1 , 8, and 15 of each 28-day cycle and TH-302 may be administered on Days 1 , 8, and 15 of each 28-day cycle.
• gemcitabine and TH-302 are administered once weekly for seven weeks followed by one week of no administration, followed by one or more 28-day cycles in which TH-302 and gemcitabine are administered on Days 1 , 8, and 15 of each 28-day cycle.
• Docetaxel may be administered IV at 75 mg/m 2 over 60 minutes.
• docetaxel may be administered IV at 75 mg/m 2 over 60 minutes on Day 1 of each 21-day cycle and TH-302 may be administered on Days 1 and 8 of each 21- day cycle.
• Pemetrexed may be administered IV at 500 mg/m 2 over 10 minutes.
• pemetrexed may be administered IV at 500 mg/m 2 over 10 minutes on Day 1 of each 21 -day cycle and TH-302 may be administered on Days 1 and 8 of each 21 -day cycle.
• Doxorubicin may administered as bolus injection at 75 mg/m 2 on Day 1 of a 21 -day cycle and TH-302 may be administered on Days 1 and 8 of each 21 -day cycle.
• the present invention provides methods for treating subjects with NSCLC of squamous cell histology by administering TH-302 in combination with pemetrexed, docetaxel, gemcitabine, a platinum-containing drug, or doxorubicin.
• TH-302 may be administered to patients with lung cancer, including SCLC, NSCLC, and NSCLC of squamous cell histology in combination with other anticancer agents.
• NSCLC of squamous cell histology is particularly refractory to chemotherapy.
• the pemetrexed-approved indications in NSCLC exclude subjects with NSCLC of squamous cell histology.
• the one patient with NSCLC of squamous cell histology treated with pemetrexed in combination with TH-302 continued on-study at Cycle 5 with stable disease.
• the present invention provides a method of treating a patient diagnosed with lung cancer (e.g., NSCLC) comprising administering a therapeutically effective dose of TH-302 in combination with a therapeutically effective dose of docetaxel.
• a patient diagnosed with lung cancer e.g., NSCLC
• administration of TH-302 and docetaxel showed antitumor activity in human patients.
• administration of a single dose of TH-302 and a single dose of docetaxel inhibited tumor growth in an H460 ectopic lung cancer model.
• Therapeutically effective doses of docetaxel may be determined by medical professionals by reference to materials available from the FDA and/or the medical literature.
• An exemplary dose for illustration and not limitation, is 75 mg/m 2 administered as a one-hour intravenous infusion.
• Illustrative therapeutically effective doses of TH-302 are described above. Other doses may be used as deemed appropriate by medical professionals and/or approved by the FDA.
• administration of docetaxel is preceded by administration of TH-302, with the gap between the end of TH-302 administration and the beginning of docetaxel administration being at least 30 minutes to one hour, typically at least 2 hours, and in any event no more than 24 hours.
• the duration of the time between TH-302 and docetaxel administrations is from 1 to 10 hours, from 2 to 6 hours, or from 3 to 5 hours.
• the gap between the end of TH-302 administration and the beginning of docetaxel administration is about 2 hours.
• the present invention also provides a method for treating a patient diagnosed with lung cancer, including NSCLC, comprising administering a therapeutically effective dose of TH-302 in combination with administering a therapeutically effective dose of pemetrexed.
• a method for treating a patient diagnosed with lung cancer including NSCLC, comprising administering a therapeutically effective dose of TH-302 in combination with administering a therapeutically effective dose of pemetrexed.
• administration of TH-302 and pemetrexed showed antitumor activity in human patients.
• infra administration of TH-302 and pemetrexed dramatically inhibited tumor growth in a NSCLC model.
• Therapeutically effective doses of pemetrexed may be determined by medical professionals by reference to materials available from the FDA and/or the medical literature.
• An exemplary dose for illustration and not limitation, is 500 mg/m 2 administered IV over 10 minutes once every three weeks.
• Illustrative therapeutically effective doses of TH-302 are described above. Other doses may be used as deemed appropriate by medical professionals and/or approved by the FDA.
• administration of pemetrexed is preceded by administration of TH-302, with the gap between the end of TH-302 administration and the beginning of pemetrexed administration being at least one hour and not more than 24 hours.
• the duration of the time between TH-302 and pemetrexed administrations is from 1 to 10 hours, from 2 to 6 hours, or from 3 to 5 hours. In some embodiments the gap between the end of TH-302 administration and the beginning of pemetrexed administration is about 2 hours.
• the present invention also provides a method for treating a patient diagnosed with lung cancer (including NSCLC) comprising administering a therapeutically effective dose of TH-302 in combination with administering a therapeutically effective dose of a platin (e.g., such as cisplatin or carboplatin).
• a platin e.g., such as cisplatin or carboplatin.
• administration of TH-302 and cisplatin inhibited tumor growth in two lung cancer models, one using H460 cells and one using Calu-6 cells.
• administration of TH-302 and carboplatin inhibited tumor growth in an H460 lung cancer model.
• Therapeutically effective doses of cisplatin and carboplatin may be determined by medical professionals by reference to materials available from the FDA and/or the medical literature.
• An exemplary dose of cisplatin, for illustration and not limitation, is 100 mg/m 2 once every four weeks.
• Therapeutically effective doses of carboplatin may be determined by medical professionals using the Calvert formula (Calvert et al., 1989, J. CHn. Oncol. 7:1748-56).
• Illustrative therapeutically effective doses of TH-302 are described above for illustration. Other doses may be used as deemed appropriate by medical professionals and/or approved by the FDA.
• administration of the platinum-containing drug is preceded by administration of TH-302, with the gap between the end of TH-302 administration and the beginning of platinum-containing drug administration being at least 30 minutes to one hour, typically at least 2 hours, and in any event no more than 24 hours.
• duration of the time between TH-302 and platinum-containing drug administrations is from 1 to 10 hours, from 2 to 6 hours, or from 3 to 5 hours.
• the gap between the end of TH-302 administration and the beginning of administration of a platinum-containing drug is about 2 hours.
• the present invention also provides a method for treating a patient diagnosed with lung cancer comprising administering a therapeutically effective dose of TH-302 in combination with administering a therapeutically effective dose of doxorubicin.
• a method for treating a patient diagnosed with lung cancer comprising administering a therapeutically effective dose of TH-302 in combination with administering a therapeutically effective dose of doxorubicin.
• administration of TH-302 and doxorubicin showed antitumor activity in human patients.
• infra administration of TH-302 and doxorubicin inhibited tumor growth in a Calu-6 lung cancer model.
• Therapeutically effective doses of doxorubicin may be determined by medical professionals by reference to materials available from the FDA and/or the medical literature.
• An exemplary dose is 40 to 75 mg/m 2 given as a single intravenous injection every 21 to 28 days.
• Therapeutically effective doses of TH-302 are described above. Other doses may be used as deemed appropriate by medical professionals and/or approved by the FDA.
• administration of doxorubicin is preceded by administration of TH-302, with the gap between the end of TH-302 administration and the beginning of doxorubicin administration being at least 30 minutes to one hour, typically at least 2 hours, and in any event no more than 24 hours.
• the duration of the time between TH-302 and doxorubicin administration is from 1 to 10 hours, from 2 to 6 hours, or from 3 to 5 hours.
• the gap between the end of TH-302 administration and the beginning of doxorubicin administration is about 2 hours.
• the present invention also provides a method for treating a patient diagnosed with lung cancer comprising administering a therapeutically effective dose of TH-302 in combination with administering a therapeutically effective dose of gemcitabine.
• a therapeutically effective dose of TH-302 in combination with administering a therapeutically effective dose of gemcitabine.
• administration of TH-302 and gemcitabine had beneficial effect in patients with, e.g., pancreatic cancer.
• Therapeutically effective doses of gemcitabine may be determined by medical professionals by reference to materials available from the FDA and/or the medical literature. An exemplary dose is 1000 mg/m 2 given i.v. over 30 minutes on days 1 , 8 and 15 of a 28 day cycle. Therapeutically effective doses of TH-302 are described above. Other doses may be used as deemed appropriate by medical professionals and/or approved by the FDA.
• administration of doxorubicin is preceded by administration of TH-302, with the gap between the end of TH-302 administration and the beginning of gemcitabine administration being at least 30 minutes to one hour, typically at least 2 hours, and in any event no more than 24 hours.
• the duration of the time between TH-302 and gemcitabine administrations is from 1 to 10 hours, from 2 to 6 hours, or from 3 to 5 hours.
• the gap between the end of TH-302 administration and the beginning of gemcitabine administration is about 2 hours.
• the present invention provides a method for treating a patient diagnosed with prostate cancer comprising administering a therapeutically effective dose of TH- 302 in combination with administering a therapeutically effective dose of a taxane such as docetaxel or paclitaxel.
• a taxane such as docetaxel or paclitaxel.
• Therapeutically effective doses of taxanes may be determined by medical professionals by reference to materials available from the FDA and/or the medical literature. For illustration and not limitation, an exemplary dose is 75-100 mg/m 2 given as an intravenous infusion once every 21 days for docetaxel and 175 mg/m 2 given as an intravenous infusion every 21 days for paclitaxel. Illustrative therapeutically effective doses of TH-302 are described above. Other doses may be used as deemed appropriate by medical professionals and/or approved by the FDA. [0140] Two human subjects with castrate resistant prostate cancer have been treated with the combination of TH-302 plus docetaxel. RECIST tumor assessments have been performed for both subjects and both subjects had stable disease.
• administration of paclitaxel or docetaxel is preceded by administration of TH-302, with the gap between the end of TH-302 administration and the beginning of paclitaxel or docetaxel administration being at least 30 minutes to one hour, typically at least 2 hours, and in any event no more than 24 hours.
• the duration of the time between TH-302 and paclitaxel or docetaxel administrations is from 1 to 10 hours, from 2 to 6 hours, or from 3 to 5 hours.
• the gap between the end of TH-302 administration and the beginning of paclitaxel or docetaxel administration is about 2 hours.
• the present invention provides a method for treating a patient diagnosed with pancreatic cancer comprising administering a therapeutically effective dose of TH-302 in combination with administering a therapeutically effective dose of gemcitabine.
• Administration of TH-302 and gemcitabine provided benefit to patients with first-line pancreatic cancer (see Example 4, infra).
• administration of TH-302 and gemcitabine dramatically inhibited tumor growth in a pancreatic cancer model (see Example 6, infra). While the maximum tolerated dose for TH-302 in combination with gemcitabine has not been established, it is anticipated to be at least 340 mg/m2. This dose is effective for treating subjects with first-line pancreatic cancer.
• Therapeutically effective doses of gemcitabine may be determined by medical professionals by reference to materials available from the FDA and/or the medical literature.
• An exemplary dose for illustration and not limitation, is 1 ,000 mg/m 2 administered IV over 30 minutes once per week.
• Illustrative therapeutically effective doses of TH-302 are described above. Other doses may be used as deemed appropriate by medical professionals and/or approved by the FDA.
• administration of gemcitabine is preceded by administration of TH-302, with the gap between the end of TH-302 administration and the beginning of gemcitabine administration being at least 30 minutes to one hour, typically at least 2 hours, and in any event no more than 24 hours.
• the duration of the time between TH-302 and gemcitabine administrations is from 1 to 10 hours, from 2 to 6 hours, or from 3 to 5 hours. In some embodiments the gap between the end of TH-302 administration and the beginning of gemcitabine administration is about 2 hours.
• the present invention provides a method for treating a patient diagnosed with a soft tissue sarcoma comprising administering a therapeutically effective dose of TH-302 in combination with administering a therapeutically effective dose of doxorubicin.
• Administration of TH-302 and doxorubicin provided benefit to patients with soft tissue sarcomas (see Example 5, infra).
• administration of TH-302 and doxorubicin inhibited tumor growth in a sarcoma model (see Example 6, infra).
• Therapeutically effective doses of doxorubicin may be determined by medical professionals by reference to materials available from the FDA and/or the medical literature.
• An exemplary dose for illustration and not limitation, is 40 to 60 mg/m 2 given as a single intravenous injection every 21 to 28 days.
• Illustrative therapeutically effective doses of TH-302 are described above.
• the maximum tolerated dose for the TH-302 in combination with a doxorubicin regimen has not been established, but subjects can be treated, in accordance with the methods of the invention at a TH-302 dose of at least 240 mg/m 2 in combination with the approved doxorubicin dose of 75 mg/m 2 .
• Other doses may be used as deemed appropriate by medical professionals and/or approved by the FDA.
• administration of doxorubicin is preceded by administration of TH-302, with the gap between the end of TH-302 administration and the beginning of doxorubicin administration being at least 30 minutes to one hour, typically at least 2 hours, and in any event no more than 24 hours.
• the duration of the time between TH-302 and doxorubicin administration is from 1 to 10 hours, from 2 to 6 hours, or from 3 to 5 hours.
• the gap between the end of TH-302 administration and the beginning of doxorubicin administration is about 2 hours.
• the present invention provides a method for treating a patient diagnosed with colon cancer comprising administering a therapeutically effective dose of TH- 302 in combination with administering a therapeutically effective dose of cisplatin.
• a therapeutically effective dose of TH- 302 in combination with administering a therapeutically effective dose of cisplatin.
• administration of TH-302 and cisplatin inhibited tumor growth in a HT-29 colon cancer model.
• the invention provides a patient diagnosed with colon cancer comprising administering a therapeutically effective dose of TH-302 and administering a therapeutically effective dose of 5-fluorouracil (5FU).
• TH-302 and 5FU inhibited tumor growth in an HT- 29 colon cancer model.
• Therapeutically effective doses of cisplatin may be determined by medical professionals by reference to materials available from the FDA and/or the medical literature.
• An exemplary dose for illustration and not limitation, is 100 mg/m 2 once every 3 to 4 weeks.
• Therapeutically effective doses of 5FU may be determined by medical professionals by reference to materials available from the FDA and/or the medical literature.
• An exemplary dose for illustration and not limitation, is 150 mg/m 2 daily.
• Illustrative therapeutically effective doses of TH-302 are described above. Other doses may be used as deemed appropriate by medical professionals and/or approved by the FDA.
• administration of 5FU or CDDP is preceded by administration of TH-302, with the gap between the end of TH-302 administration and the beginning of 5FU or CDDP administration being at least 30 minutes to one hour, typically at least 2 hours, and in any event no more than 24 hours.
• the duration of the time between TH-302 administration and administration of 5FU or CDDP is from 1 to 10 hours, from 2 to 6 hours, or from 3 to 5 hours.
• the gap between the end of TH-302 administration and the beginning of 5FU or CDDP administration is about 2 hours.
• the methods of the invention also include combination therapies with other compounds of Formula I, including, without limitation, TH-281.
• the therapeutically effective dose may vary depending on which compound of Formula I is selected, the dose will typically be an amount in the range of about 200 mg/m 2 - about 700 mg/m 2 , about 300 mg/m 2 - about 600 mg/m 2 , about 350 mg/m 2 - about 550 mg/m 2 , about 400 mg/m 2 - about 500 mg/m 2 , about 400 mg/m 2 - about 600 mg/m 2 , and about 450 mg/m 2 - about 550 mg/m 2 .
• the dose administered is about 560 mg/m 2 , 480 mg/m 2 , 400 mg/m 2 , 340 mg/m 2 , 240 mg/m 2 , or 120 mg/m 2 . In other embodiments, the dose administered is in an amount in the range of about 700 mg/m 2 - about 1200 mg/m 2 or about 800 mg/m 2 - about 1000 mg/m 2 .
• Example 1 describes formulations of the invention.
• Example 2 describes TH-302 monotherapy.
• Example 3 demonstrates the advantages of administering a HAP prior to administering another anti-cancer agent and incorporating a delay period between administrations.
• Examples 4 and 5 demonstrate the efficacy of TH-302 combination therapies in treating human cancers in human patients. In human trials lyophilized TH-302 was resuspended in D5W for administration to patients.
• Example 6 demonstrates the efficacy of TH-302 combination therapies in treating human cancers in animal models.
• Example 1 Pharmaceutical Formulations of TH-302
• This example describes pharmaceutical formulations of TH-302 as well as the results of experimentation demonstrating the advantages of certain formulations As discussed below a formulation containing TH-302, ethanol and TWEEN 80 provided advantages over other formulations including higher solubility of TH-302, allowing for a more concentrated solution, greater stability on storage and the absence of precipitation when the concentrated formulation is diluted into D5W or saline
• the materials and reagents were TH-302, prepared under GMP by Syngene, anhydrous 200 proof Sigma-Ald ⁇ ch Cat No 459836-2L ethyl alcohol, HPLC grade or equivalent acetonitrile and water, benzyl alcohol Sigma-Ald ⁇ ch Cat No 108006-100 ml, N,N-d ⁇ methylacetam ⁇ de (DMA) Sigma-Aldrich Cat No 185884-50OmI, and 2 ml Vial Labfile AMB Wheaton Cat No W224681
• TH-302 formulations were subjected to different conditions to produce partial degradation
• the test solutions and standards were individually stressed under the same conditions
• Test solutions for evaluation were prepared according to the procedures described below
• a following series of comparative formulations (1 2A and 2B) were prepared to evaluate the stability of TH-302 using various combinations of the indicated solvents (ethanol (EtOH) and in DMA/EtOH/Benzyl alcohol) without a nonionic surfactant. These formulations were studied in accelerated stability conditions at various temperatures (4 0 C, 2O 0 C 1 and 37 0 C) for up to 154 days.
• Formulation 1 was prepared as follows. A 50 mg/ml solution of TH-302 in EtOH was prepared. 2.5 g of TH-302 were weighed out and transferred into a volumetric flask (50 ml). 46 ml of EtOH were added and the mixture was stirred at room temperature for 1.5 hours.
• the solution was diluted to 50 ml by the addition of ethanol.
• the solution was transferred into 2-ml vials with 1 ml of solution in each vial.
• the concentration was 50 mg/ml.
• the vials were stored at different temperatures (4°C (refrigerator); 2O 0 C (bench); 37 0 C (water bath)) for the various times shown below. Samples were taken on days 28, 65, 106 and 154 for LC analysis.
• 50 ⁇ l_ was aliquoted from the 50 mg/ml TH 302 solutions, added to volumetric flasks (50 ml), and diluted with water to the 50 ml volume and mixed well. The concentration was 50 ⁇ g/ml.
• Formulation 2A was prepared as follows. 1.2 g of TH-302 was weighed out and transferred into a solution of benzyl alcohol (600 mg) and DMA (1200 mg) in a volumetric flask (10 ml). The mixture became a clear solution after agitating for 5 min. The solution was diluted to 10 ml by the addition of ethanol. The solution was transferred into 2 ml vials with 0.2 ml solution in each vial. The TH-302 concentration was 120 mg/ml. The vials were stored at different temperatures (4 0 C (refrigerator); 2O 0 C (bench); 37 0 C (water bath)) for the various times shown below.
• Formulation 2A that was at 4 0 C was warmed to room temperature (RT) and kept at this temperature for 30 min.
• Formulation 2A at 37 0 C was cooled down to RT kept at this temperature for 30 min.
• 20 ⁇ L of the 120 mg/ml TH 302 solutions from each vial stored at different temperatures (4 0 C; 2O 0 C; 37 0 C) was transferred into a corresponding volumetric flask (50 ml). The solutions were then diluted with water to the 50 ml volume and mixed well. The final concentration of TH-302 was 48 ⁇ g/ml.
• Formulation 2B was prepared using the same procedure as for preparing solution 2A, except the amount of DMA was reduced to 1000 mg.
• TH-302 is stable in DMA/EtOH/Benzyl alcohol (120 mg/ml) at 4 0 C and room temperature (RT) for at least 10 weeks (67 days). Crystals of TH-302 were observed in 4°C samples and dissolved upon warming to RT for 30 min. Two impurities (for a total of about 3%) were observed after TH-302 was incubated at 37 0 C for 4 weeks in DMA/EtOH/Benzyl alcohol. One of the impurities (0.25%) was observed at RT after 10 weeks. The other impurity was the monochloro compound, which was present at time zero and did not notably increase. No difference between formulations 2A and 2B was observed.
• TH-302 is has similar stability in EtOH and in DMA/EtOH/Benzyl alcohol.
• This study evaluated the stability of a 200 mg/ml TH-302 solution in PEG 400 without a nonionic surfactant (Formulation 3) for 4 weeks at 37 0 C.
• Formulation 3 was made with 2 g of TH-302, which was transferred into PEG-400 (10 ml). The mixture became a clear solution after agitating at 4O 0 C for 15 min. The solution was transferred into 2 ml vials with 0.2 ml solution in each vial. The concentration of TH- 302 was 200 mg/ml.
• the vials were stored at different temperatures (2-8 0 C (refrigerator, i.e., 4 0 C); 37 0 C (water bath)) for the various times shown below.
• This stock solution was cooled down to RT and kept at this temperature for 30 min.
• 20 ⁇ L of the 200 mg/ml TH 302 solutions were transferred into a volumetric flask (50 ml).
• the solutions were then diluted with water to the 50 ml volume and mixed well.
• the final concentration of TH-302 was 80 ⁇ g/ml. 19 ml of water was injected into this solution in a 100 ml vial and a dark brown clear solution was obtained.
• Another comparative of Formulation 4 an aqueous solution of lyophilized TH-302 without a nonionic surfactant was conducted. The following procedure was used to prepare Formulation 4. 19 ml of water were injected into the TH-302 in a 100 ml vial and a dark brown clear solution was obtained. 50 ⁇ L of the resulting solution was transferred into a volumetric flask (5 ml) and diluted with water to 5 ml. The final concentration of TH-302 was 50 ⁇ g/ml.
• One formulation of TH-302 that has been used in human clinical trials is a lyophilized powder that is stored at -2O 0 C and reconstituted just prior to patient administration (reconstituted lyophilized product).
• HPLC analysis was used to analyze the relative stability of Formulations 1-4 at 37 0 C after 28 days. The results are shown in the following table.
• TH-302 Based on the stability data at 37 0 C on day 28, TH-302 has the following stability order in the various formulations: Ethanol > Ethanol/Benzyl alcohol/DMA > PEG-400 » reconstituted lyophilized product.
• Formulations of TH-302 in pure DMA proved to be problematic when the drug solution was reconstituted in saline or D5W.
• Formulations of TH-302 in DMA/PEG-400 proved to be problematic when the drug solution was reconstituted in saline or D5W.
• Vehicle A was prepared as follows: Into a 20 ml vial was added a mixture of EtOH (4 ml), DMA (0.75 mi) and TWEEN 80 (0.25 ml). The mixture was then well mixed by stirring for 5 min.
• Vehicle B was prepared as follows: Into a 20 ml vial was added a mixture of EtOH (3.75 ml), DMA (1.0 ml) and TWEEN 80 (0.25 ml). The mixture was then well mixed by stirring for 5 min.
• Vehicle C was prepared as follows: Into a 20 ml vial was added a mixture of EtOH (3.5 ml), DMA (1.25 ml) and TWEEN 80 (0.25 ml). The mixture was then well mixed by stirring for 5 min.
• Vehicle D was prepared as follows: Into a 20 ml vial was added a mixture of EtOH (4.25 ml), DMA (0.25 ml). The mixture was then well mixed by stirring for 5 min.
• 100 mg/ml solutions were prepared as follows: 50 mg of TH-302 was allowed to dissolve in 0.5 ml of vehicle A, B, C 1 D in a corresponding 2 ml vial. The mixture in each vial was stirred for 5 min and a clear solution was obtained from all the vehicles.
• 150 mg/ml solutions were prepared as follows: 75 mg of TH-302 was allowed to dissolve in 0.5 ml of vehicle A, B, C, D in a corresponding 2 ml vial. The mixture in each vial was stirred for 5 min and a clear solution was obtained from all the vehicles. 200 mg/ml solutions were prepared as follows: 100 mg of TH-302 was allowed to dissolve in 0.5 ml of vehicle A, B, C, D in a corresponding 2 ml vial. The mixture in each vial was stirred for 10 min and a clear solution was obtained from all the vehicles.
• TH-302 in the six formulations is significantly more stable than in the reconstituted lyophilized drug product formulation (DP; lyophilized TH-302 reconstituted in D5W), when the solutions were stored at 25 0 C.
• DP lyophilized TH-302 reconstituted in D5W
• Three out of the 6 formulations showed only minimum degradation of TH-302 over 31 days when compared with TH-302 in the DP formulation under the similar conditions, which showed over 18% degradation.
• TWEEN 80 allowed for a more concentrated formulation of TH-302 and was shown to stabilize TH-302 better than the other formulations at similar concentrations.
• TH-302 has good solubility in these formulations (up to 300 mg/ml) depending on the ratio of DMA/Ethanol/TWEEN 80. While increasing the concentration of DMA in the vehicle enhances the solubility of TH-302 in the liquid formulation, may affect the chemical stability of TH-302 in the formulation. TWEEN 80 prevented TH-302 precipitation when the drug solution was reconstituted in saline or D5W. Based on these results, a combination of nonionic surfactant, ethanol, and optionally DMA provides a concentrated formulation of TH-302 with suitable stability for long-term storage.
• EXAMPLE 2 Treatment of Lung Cancer and Melanoma in Human Patients Using TH- 302 Monotherapy
• a Phase 1 clinical trial was conducted with TH-302. The starting dose was 7.5 mg/m 2 IV over 30-60 min administered once weekly for 3 weeks of a 4 week cycle. A modified accelerated titration design was used. Two of five patients dosed at 670 mg/m 2 exhibited dose limiting toxicity (DLT): herpes simplex perianal/rectal ulcers and dehydration due to mucositis. Six patients were enrolled at an intermediate dose of 575 mg/m 2 , and this dose was established as the MTD for this administration schedule, as five of the six patients did not exhibit a DLT at this dose. [0183] There was evidence of anticancer activity even at the lowest dose, with one NSCLC patient exhibiting stable disease (SD) for 7.3 months. Two patients, one with SCLC treated at 480 mg/m 2 and another with melanoma treated at 670 mg/m 2 , had unconfirmed partial responses, as described in more detail below; 16 patients had stable disease.
• SD stable disease
• TH-302 is co-administered with an agent that prevents or ameliorates skin and/or mucosal toxicity.
• AEs TH-302-related adverse events
• TH-302 was diluted with D5W and administered to the patient at an amount of 480 mg/m 2 , according to the following 4 week dosing cycle: TH-302 was administered once every week for 3 weeks, on days 1 , 8, and 15, followed by a week of no TH-302 administration. The patient was administered 2 cycles (i.e. 6 doses) of TH-302, and the lung and liver cancers assessed by a computed tomography (or CT) scan.
• CT computed tomography
• the CT scan demonstrated that the cancer in lung and liver had reduced in area by over 50% (44% decrease in sum of the longest diameters [SLD] of target lesions). LDH had decreased 72%, and liver function tests had normalized.
• the Cycle 2 tumor assessment also showed a large empyema that required surgical intervention, and a 22-day delay of Cycle 3 dosing. Confirmation CT scan one month after the Cycle 2 scan showed progressive disease.
• TH-302 was administered to the patient at an amount of 670 mg/m 2 using a 4 week (28 day) dosing cycle: TH-302 was administered once every week for 3 weeks, on days 1 , 8, and 15, followed by a week of no TH-302 administration. The patient was administered 2 cycles of TH-302 and assessed by a CT scan. The CT scan demonstrated that the cancer in lung and liver had reduced in area by over 50% (53% decrease in SLD of target lesions).
• Enrollment in the study was expanded at the MTD in patients with metastatic melanoma.
• TH-302 was administered intravenously over 30-60 minutes on Days 1 , 8 and 15 of a 28-day cycle.
• Eligible patients had ECOG ⁇ 1 , at least one target lesion by RECIST, and acceptable hematologic, liver, and renal function. Patients with symptomatic brain metastases were excluded unless previously treated and well controlled for at least 3 months.
• Nine patients with metastatic melanoma have been treated in the study. The median age was 70 (range 23-78) with 5 females and 4 males and ECOG 0/1 in 4/5 patients.
• Four patients had an elevated baseline LDH. Metastatic sites included liver in 7 patients and lung in 6 patients.
• EXAMPLE 3 Effect of Administration Schedule for HAP and Non-HAP Chemotherapeutic Agents in Combination Therapy
• Randomization and dosing was initiated when tumors reached a certain size (100 - 150 mm 3 ).
• API grade of TH-302 was used in all experiments while docetaxel, gemcitabine, cisplatin, pemetrexed, and doxorubicin were purchased from commercial sources.
• TH-302/docetaxel dosing regimens in the H460 tumor growth (NSCLC) model was examined.
• the H460 cells were prepared in 30% Matrigel and 70% RPMI1640. Mice were anesthetized by isoflurane and were implanted subcutaneously with 1 x 10 6 cells (in 200 ⁇ l) at the flank position. We selected 110 mice bearing similar size tumors (-100 mm 3 ) for the study. Mice bearing similar tumor size were randomly assigned into different groups. Treatment started on day 1 (7 days after tumor implantation) except as noted.
• TH-302 was administered intraperitoneally (IP) at 150 mg/kg, and docetaxel was administered intravenously (IV) at 10 mg/kg.
• IP intraperitoneally
• IV intravenously
• TGD tumor growth delay
• TGI tumor growth inhibition
• results showed that, in general, TH-302 given before docetaxel produced a superior antitumor response, and administration of TH-3024 hours before the chemotherapeutic was better than the other time intervals tested, e.g. 24 or 48 hours before, or simultaneously.
• the cells implanted were PC-3 human prostate cancer cells and 3 x 10 6 cells were implanted and mice were randomized into separate groups when their tumors reached ⁇ 150mm 3 TH-302 first provided the best results.
• the results for the 2, 4, and 24 hour delay tests are included in Table 19, below.
• TH-302 Administering the non-HAP drug (cisplatin) drug 2 hours after the administration of the HAP drug (TH-302) demonstrated the best treatment efficacy, when compared to contemporaneous administration or when the cisplatin was administered before the HAP drug with a 2 hour.
• TH-302 administered contemporaneously with docetaxol in the PC-3 prostate cancer model showed toxic side effects in the mice, and 6 out of 10 mice tested with this administration schedule were sacrificed due to >20% body weight loss.
• TH-302 was administered to CD1 mice, and gemcitabine was then administered 0, 2, 4, 8, 16, or 24 h after stopping the administration of TH-302.
• the safety of the combination administration was measured by its effect on in blood cell counts (white blood cells or WBC, neutrophil, lymphocytes, monocyte, red blood cells or RBC, and hemoglobin or Hb) 2 days after the administration of TH-302 (the higher the blood cell count, the safer being the administration of the drugs in combination). Both drugs were administered intraperitoneal ⁇ ; TH-302 was administered at a dose of 75 mg/kg, and gemcitabine was administered at 300 mg/kg.
• the results demonstrated that non- contemporaneous administration of TH-302 and gemcitabine, for example, when gemcitabine was administered 2 h or 4 h after the administration of TH-302, was less toxic than administering them together.
• EXAMPLE 4 Combination Therapy with TH-302 and Gemcitabine, Docetaxel, or Pemetrexed
• This Example demonstrates the non-contemporaneous administration of an anticancer agent other than TH-302 in combination with TH-302 for the treatment of cancer.
• a Phase 1/2, 3-arm, multicenter, dose-escalation study was conducted using a classic dose escalation design to demonstrate the efficacy and determine the safety of TH-302 when administered in combination with gemcitabine, docetaxel, or pemetrexed.
• the initial dose of TH-302 was 240 mg/m 2 TH-302 was administered by intravenous (IV) infusion over 30 minutes on Days 1 , 8, and 15 of a 28-day (4 week) cycle (Arm A) or Days 1 and 8 of a 21 -day (3 week) cycle (Arms B & C) as noted below.
• IV intravenous
• Gemcitabine docetaxel or pemetrexed was administered 2 h after the TH-302 infusion was completed The starting doses of gemcitabine, docetaxel or pemetrexed remained fixed according to approved doses listed in their respective product labeling
• the treatment regimen, dose, schedule and cycle length of these drugs were as follows
• Treatment Arm A Gemcitabine was administered IV at 1 ,000 mg/m 2 IV over 30 minutes on Days 1 , 8, and 15 of each 28-day cycle.
• TH-302 was administered as above on Days 1 , 8, and 15 of each 28-day cycle.
• Treatment Arm B Docetaxel was administered IV at 75 mg/m 2 over 60 minutes on Day 1 of each 21-day cycle.
• TH-302 was administered as above on Days 1 and 8 of each 21 -day cycle.
• Treatment Arm C Pemetrexed was administered IV at 500 mg/m 2 over 10 minutes on Day 1 of each 21 -day cycle TH-302 was administered as above on Days 1 and 8 of each 21 -day cycle.
• MTD maximum tolerated dose
• CT scans were done every 2 cycles.
• the objectives of the study were to determine the MTD and DLT of TH-302 and to evaluate the safety, pharmacokinetics (PK) and preliminary efficacy of TH-302 in combination with gemcitabine (G), docetaxel (D), or pemetrexed (P) in advanced solid tumors.
• Seventy-two patients have been enrolled and have sufficient follow-up to be included in the dose escalation summary.
• Fifty patients were enrolled with sufficient tumor assessment follow-up. Patients were enrolled at 7 US sites from August 2008 to August 2009 and received study drug. Study drug exposure and DLTs are summarized below.
• the MTD of TH-302 plus gemcitabine is anticipated to be 340-400 mg/m 2 ; the MTD of TH-302 plus docetaxel is 340 mg/m 2 and the MTD of TH-302 plus pemetrexed is 480 mg/m 2 .
• the primary dose limiting toxicities have been hematologic. While the contribution of TH-302 to the hematologic toxicity is hard to determine when TH-302 is combined with a myelosuppressive chemotherapy, greater hematologic toxicity than would be expected with single agent chemotherapy is evident in the gemcitabine and pemetrexed arms. Skin and mucosal toxicity are common at doses above 240 mg/m 2 .
• TH-302 The mechanism is unknown but may be due to activation of TH-302 in areas of epithelium that are normally hypoxic.
• TH-302 to standard chemotherapies does not appear to enhance the toxicity in other body systems. Higher response rates than would be expected with single agent chemotherapy are evident.
• TH-302 was administered intravenously for 30 to 60 minutes on days 1 , 8 and 15 of a 28 day cycle.
• Gemcitabine is dosed according to its package insert on days 1 , 8 and 15 of a 28 day cycle.
• the TH-302 maximum tolerated dose (MTD) has not been established with the dose cohort currently being expanded at 340 mg/m 2 .
• Two dose limiting toxicities were reported at each of two higher TH-302 doses levels. Fifteen patients have had tumor assessments, 6 of whom had a PR in the following cancers: pancreatic (2), ovarian, esophageal, squamous non-small cell lung cancer (NSCLC) and thyroid and 7 patients with SD.
• NSCLC non-small cell lung cancer
• CA 19-9 responses defined as a greater than 50% decrease from the baseline CA19-9, have been shown to predict for a better prognosis.
• Two of the four subjects had an elevated CA19-9 prior to the combination therapy. Both of these subjects had CA19-9 responses with CA19-9 decreases of 78% and 98%.
• TH-302 was administered intravenously on days 1 and 8 of a 21 day cycle. Docetaxel was dosed according to its package insert on day 1 of the 21 day cycle.
• the TH-302 MTD has been established at 340 mg/m 2 and the dose expansion has been initiated at this dose in patients with castrate resistant prostate cancer and in patients with second-line NSCLC. Eleven patients have had tumor assessments, 2 of whom achieved PRs in NSCLC and anal cancer and 6 patients with SD.
• TH-302 was administered intravenously on days 1 and 8 of a 21 day cycle. Pemetrexed was dosed according to its package insert on Day 1 of the 21 day cycle.
• the TH-302 MTD has been established at 480 mg/m 2 and the dose expansion has been initiated at a TH-302 dose of 400 mg/m 2 in patients with second-line non-squamous NSCLC.
• Nineteen patients have had tumor assessments, 4 of whom achieved PRs in NSCLC (2) and transitional cell carcinoma (2) and 9 patients with SD.
• EXAMPLE 5 Combination Therapy with TH-302 and Doxorubicin [0214]
• a Phase 1/2, multicenter, dose-escalation study of patients with soft tissue sarcoma using a classic dose escalation design was conducted to demonstrate the efficacy and safety of TH-302 when administered in combination with doxorubicin in accordance with the present invention.
• the dose of TH-302 was escalated in cohorts of 3-6 subjects.
• the initial dose of TH-302 was 240 mg/m 2 , a dose with no Cycle 1 grade 2 or greater toxicity (excluding fatigue, nausea, vomiting, alopecia, and diarrhea) in the single agent Phase 1 study.
• a Dose Level minus 1 was built into the study.
• a subject experienced a DLT 3 additional subjects were enrolled at that dose level for a total of 6 subjects in that cohort. If no additional DLTs were observed, dose escalation resumed. However, if 2 or more of 6 subjects within a cohort experience a DLT, that dose will be considered to exceed the MTD. The MTD will then be defined at the next lower dose level whereby 6 subjects are treated and ⁇ 1 subject experiences a DLT.
• the maximum dose of TH-302 is the single agent MTD or the highest dose tested in that study if the MTD was not reached. MTD is based on toxicities occurring during the first cycle.
• TH-302 was administered by IV infusion over 30-60 minutes on Days 1 and 8 of a 21 day cycle.
• the dose of doxorubicin remained fixed: 75 mg/m 2 administered by bolus injection starting on Day 1 of a 21 -day cycle (if serum bilirubin is above the ULN but ⁇ 1.5 xULN, the dose was reduced to 56 mg/m 2 ).
• Doxorubicin was administered starting two hours after completion of TH-302 infusion on Day 1 of each cycle.
• GCSF granulocyte-stimulating factor
• RECIST tumor assessments have been performed for seven subjects. Three of seven subjects had partial responses and another three of these same seven subjects have had stable disease. The historical response rate in first-line soft tissue sarcoma is between 15% and 25%. Two of the seven subjects continue on- study and are receiving Cycle 4 or Cycle 11. All three subjects with partial responses continued on-study to receive TH-302 alone after completing the doxorubicin component of the study.
• EXAMPLE 6 Combination Therapies With TH-302 in Cancer Models
• This example demonstrates that the methods of the invention for combination therapy of cancer with HAP and non-HAP anticancer agents have anticancer activity superior to either agent by itself.
• ectopic, orthotopic and metastatic models were employed in nude mice.
• Anti-tumor activity was evaluated by tumor growth inhibition (TGI) and tumor growth delay (TGD).
• TGI tumor growth inhibition
• TTD tumor growth delay
• TH-302 was tested as monotherapy and in combination with Taxol (paclitaxel) in animals bearing highly invasive and metastatic orthotopic prostate cancer PC-3 cells. Animals were randomized into 6 groups of 8 mice each and then treated either with vehicle; Taxol (12 mg/kg, IV, twice a week for 4 consecutive weeks); TH-302 (30 or 50 mg/kg, IP, once a day for 5 days a week for 2 consecutive weeks); or Taxol in combination with TH-302 (using the same single agent regimens). The study demonstrated significant response rates with the combination therapy, at either dose of TH-302, in which disease progression is tracked by tumor volume. Taxol alone and TH-302 alone at either the 30 or 50 mg/kg dose significantly inhibited primary tumor growth during the treatment period.
• Taxol paclitaxel

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