Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
  • A61K31/5375—1,4-Oxazines, e.g. morpholine
  • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/63—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide
  • A61K31/635—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide having a heterocyclic ring, e.g. sulfadiazine
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
  • 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
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
  • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
  • A61P35/02—Antineoplastic agents specific for leukemia
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
  • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Definitions

• AML acute myeloid leukemia
• MDS myelodysplastic syndrome
• the polo-like kinase (PLK) family of serine/threonine kinases comprises at least four known members: PLK1, PLK2 (also known as Snk), PLK3 (also known as Fnk or Prk) and PLK4 (also known as Sak).
• Agents which inhibit PLK4 have the potential to treat cancer.
• PLK1, PLK2 also known as Snk
• PLK3 also known as Fnk or Prk
• PLK4 also known as Sak
• Agents which inhibit PLK4 have the potential to treat cancer.
• a number of potent PLK4 inhibitors are disclosed in U.S. Patent Nos. 8,263,596, 8,481,525, and 8,481,533 (the entire teachings of which are incorporated herein by reference). The structure of one inhibitor disclosed in these patents is shown below as Compound (I).
• AML Acute myeloid leukemia
• EPN European Leukemia Net
• MDS Myelodysplastic Syndromes
• AML acute myeloid leukemia
• Chronic myeloid leukemia is also known as chronic myelogenous leukemia. It is a type of cancer that starts in certain blood-forming cells of the bone marrow.
• CML chronic myelogenous leukemia
• a genetic change takes place in an early (immature) version of myeloid cells — the cells that make red blood cells, platelets, and most types of white blood cells (except lymphocytes).
• BCR-ABL This change forms an abnormal gene called BCR-ABL, which turns the cell into a CML cell.
• the leukemia cells grow and divide, building up in the bone marrow and spilling over into the blood. In time, the cells can also settle in other parts of the body, including the spleen.
• CML is a fairly slow growing leukemia, but it can change into a fast - growing acute leukemia that's hard to treat.
• Compound (I) has potent anticancer activity against acute myeloid leukemia, acute lymphoblastic leukemia (ALL), chronic myeloid leukemia (CLL), non-Hodgkin’s lymphoma (NHL), Burkitt lymphoma, or diffuse large B- cell lymphoma (DLBCL), or myelodysplastic syndrome. Additionally, it has now been found that Compound (I) has additive/synergistic activity towards multiple complex karyotype (CK) AML cell lines in vitro in combination with standard of care agents Venetoclax (Bcl2 inhibitor) and 5-Azacytidine (also known as azacitidine).
• ALL acute lymphoblastic leukemia
• CLL chronic myeloid leukemia
• NHL non-Hodgkin’s lymphoma
• NHL non-Hodgkin’s lymphoma
• Burkitt lymphoma Burkitt lymphoma
• DLBCL diffuse large B- cell lymphoma
• Compound (I) positively affected the outcome of a patient with CK AML. Based on these discoveries, methods of treating AML, CLL, NHL, Burkitt lymphoma, DLBCL, or MDS (including complex karyotype of each disease) with Compound (I) are disclosed herein.
• the present disclosure provides a method of treating a subject with acute myeloid leukemia, chronic myeloid leukemia, non-Hodgkin’s lymphoma, Burkitt lymphoma, or diffuse large B-cell lymphoma, or myelodysplastic syndrome, comprising administering an effective amount of Compound (I): or a pharmaceutically acceptable salt thereof.
• the present disclosure provides the use of Compound (I) or a pharmaceutically acceptable salt thereof for the manufacture of a medicament for treating a subject with acute myeloid leukemia, chronic myeloid leukemia, non-Hodgkin’s lymphoma, Burkitt lymphoma, or diffuse large B-cell lymphoma, or myelodysplastic syndrome.
• the present disclosure provides Compound (I) or a pharmaceutically acceptable salt thereof for treating a subject with acute myeloid leukemia, chronic myeloid leukemia, non-Hodgkin’s lymphoma, Burkitt lymphoma, or diffuse large B- cell lymphoma, or myelodysplastic syndrome.
• FIG. 1 shows Compound (I) treatment of cancer cells causes aberrant mitoses leading to death or arrest.
• FIG. 2 shows tumor volume (MOLT-4) in SCID mice vs treatment day.
• FIG. 3 shows the body weight (SCID mice) vs treatment day.
• FIG. 4 shows tumor volume (MV4-11) in SCID mice vs treatment day.
• FIG. 5 shows the body weight (SCID mice) vs treatment day.
• Compound (I) refers to a compound having a chemical name (li?,2 ⁇ S)-2-(3-((£)-4-(((2 ⁇ S',6i?)-2,6-dimethylmorpholino)methyl)styryl)-li/-indazol-6-yl)-5'- methoxyspiro [cyclopropane- l,3'-indolin]-2'-one, which has the following structure:
• Compound (I) was developed as a PLK 4 inhibitor and is disclosed in WO2011/123946.
• the preparation of Compound (I) is described in Example A185 of WO2011/123946, the entire teachings of which are incorporated herein by reference.
• Suitable pharmaceutically acceptable acid addition salts of the compounds of the invention include salts of inorganic acids (such as hydrochloric acid, hydrobromic, phosphoric, metaphosphoric, nitric, and sulfuric acids) and of organic acids (such as, acetic acid, benzenesulfonic, benzoic, citric, ethanesulfonic, fumaric, gluconic, glycolic, isethionic, lactic, lactobionic, maleic, malic, methanesulfonic, succinic, p- toluenesulfonic, and tartaric acids).
• inorganic acids such as hydrochloric acid, hydrobromic, phosphoric, metaphosphoric, nitric, and sulfuric acids
• organic acids such as, acetic acid, benzenesulfonic, benzoic, citric, ethanesulfonic, fumaric, gluconic, glycolic, isethionic, lactic, lactobionic, maleic,
• Compounds of the invention with acidic groups such as carboxylic acids can form pharmaceutically acceptable salts with pharmaceutically acceptable base(s).
• suitable pharmaceutically acceptable basic salts include ammonium salts, alkali metal salts (such as sodium and potassium salts) and alkaline earth metal salts (such as magnesium and calcium salts).
• Compounds with a quaternary ammonium group also contain a counteranion such as chloride, bromide, iodide, acetate, perchlorate and the like.
• salts include hydrochlorides, hydrobromides, sulfates, methanesulfonates, nitrates, maleates (between Compound (I) and maleic acid is 1:1 or 2:1), acetates, citrates, fumarates (molar ratio of between Compound (I) and fumaric acid is 1:1 or 2:1), tartrates [e.g. (+)-tartrates, (-)-tartrates or mixtures thereof including racemic mixtures], succinates, benzoates and salts with amino acids such as glutamic acid.
• the present disclosure provides Compound (I) as a fumarate salt.
• the molar ratio between Compound (I) and fumaric acid is 1 : 1.
• crystal forms of Compound (I) or the corresponding pharmaceutically acceptable salt are also included in the present disclosure.
• the crystal forms and their preparation methods are disclosed in WO2015/054793 and WO2020/215155, the entire teachings of which are incorporated herein by reference.
• Stereoisomers are compounds which differ only in their spatial arrangement.
• the stereoiso meric purity of the compounds used in the disclosed methods are at least 60%, 70%, 80%, 90%, 99% or 99.9% by weight.
• the stereoisomeric purity in this case is determined by dividing the total weight in the mixture of the stereoisomers encompassed by the name or structure by the total weight in the mixture of all of the stereoisomers.
• an effective amount means an amount when administered to the subject which results in beneficial or desired results, including clinical results, e.g., inhibits, suppresses or reduces the cancer (e.g., as determined by clinical symptoms or the amount of cancer cells) in a subject as compared to a control.
• “treating a subject with a cancer” includes achieving, partially or substantially, one or more of the following: arresting the growth or spread of a cancer, reducing the extent of a cancer (e.g., reducing size of a tumor or reducing the number of affected sites), inhibiting the growth rate of a cancer, and ameliorating or improving a clinical symptom or indicator associated with a cancer (such as tissue or serum components).
• an effective amount of a compound of the invention varies depending upon various factors, such as the given drug or compound, the pharmaceutical formulation, the route of administration, the type of disease or disorder, the identity of the subject or host being treated, and the like, but can nevertheless be routinely determined by one skilled in the art.
• An effective amount of a compound of the present invention may be readily determined by one of ordinary skill by routine methods known in the art.
• an effective amount of a compound of the invention ranges from about 0.01 to about 1000 mg/kg body weight, alternatively about 0.05 to about 500 mg/kg body weight, alternatively about 0.1 to about 100 mg/kg body weight, alternatively about 0.1 to about 15 mg/kg body weight, alternatively about 1 to about 5 mg/kg body weight, and in another alternative, from about 2 to about 3 mg/kg body weight.
• the skilled artisan will appreciate that certain factors may influence the dosage required to effectively treat a subject suffering from cancer and these factors include, but are not limited to, the severity of the disease or disorder, previous treatments, the general health and/or age of the subject and other diseases present.
• the term “treat,” “treating,” or “treatment,” when used in connection with a disorder or condition includes any effect, e.g., lessening, reducing, modulating, ameliorating, and/or eliminating, that results in the improvement of the disorder or condition. Improvements in or lessening the severity of any symptom of the disorder or condition can be readily assessed according to standard methods and techniques known in the art.
• the term “refractory” means a cancer that does not respond to treatment.
• the cancer may be resistant at the beginning of treatment or it may become resistant during treatment.
• complex karyotype is defined by the presence of >3 chromosomal aberrations (structural and/or numerical) identified by using chromosome banding analysis (CBA).
• AML is the most common type of acute leukemia. It occurs when the bone marrow begins to make blasts, cells that have not yet completely matured. These blasts normally develop into white blood cells. However, in AML, these cells do not develop and are unable to ward off infections.
• the bone marrow may also make abnormal red blood cells and platelets.
• the number of these abnormal cells increases rapidly, and the abnormal (leukemia) cells begin to crowd out the normal white blood cells, red blood cells and platelets that the body needs.
• AML AML
• AML AML
• leukemia AML
• eight different subtypes which are based on the cell that the leukemia developed from The types of acute myelogenous leukemia include:
• Complex karyotype acute myeloid leukemia is acute myeloid leukemia characterized by at least three chromosome abnormalities. Abnormalities found in complex karyotype acute myeloid leukemia include in loss of material from the 5q, 7q and/or 17p chromosome arms and is referred to herein as “typical CK”.
• atypical CK TP53, PHF6, FLT3-TKD, MED 12 , NPM1, DNMT3A, NF1, NR AS, IDH2, RUNX1, NPM1, SRSF2, ZRSR2, ASXLland FLT3-ITD mutations are associated with atypical CK. Treatment of both is contemplated by the disclosed methods. Also included with the disclosed methods are patients with some or all of the mutations associated with typical and atypical CK.
• AML to be treated is relapsed or refractory. In some embodiments, AML to be treated is complex karyotype acute myeloid leukemia.
• the myelodysplastic syndrome to be treated is relapsed or refractory. In some embodiments, myelodysplastic syndrome to be treated is complex karyotype myelodysplastic syndrome.
• the acute lymphoblastic leukemia to be treated is relapsed or refractory.
• ALL to be treated is complex karyotype acute lymphoblastic leukemia.
• the acute lymphoblastic leukemia to be treated is T-cell acute lymphoblastic leukemia. In some embodiments, the acute lymphoblastic leukemia to be treated is B-cell acute lymphoblastic leukemia.
• the chronic myeloid leukemia to be treated is relapsed or refractory.
• CML to be treated is complex karyotype acute lymphoblastic leukemia.
• the non-Hodgkin’s lymphoma to be treated is relapsed or refractory. In some embodiments, non-Hodgkin’s lymphoma to be treated is complex karyotype non-Hodgkin’s lymphoma.
• the Burkitt lymphoma to be treated is relapsed or refractory. In some embodiments, Burkitt lymphoma to be treated is complex karyotype Burkitt lymphoma.
• the diffuse large B-cell lymphoma to be treated is relapsed or refractory. In some embodiments, diffuse large B-cell lymphoma to be treated is complex karyotype diffuse large B-cell lymphoma.
• the diffuse large B-cell lymphoma to be treated is germinal center B cell-like. In some embodiments, the diffuse large B-cell lymphoma to be treated is activated B cell-like.
• the present teachings provide methods of treating a subject with acute myeloid leukemia, chronic myeloid leukemia, non-Hodgkin’s lymphoma, Burkitt lymphoma, or diffuse large B-cell lymphoma, or myelodysplastic syndrome comprising administering to the subject an effective amount of Compound (I) in combination with an additional therapeutic agent.
• the additional therapeutic agent is an anti-cancer drug.
• an “anti-cancer drug” is a compound, which when administered in an effective amount to a subject with cancer, can achieve, partially or substantially, one or more of the following: arresting the growth, reducing the extent of a cancer (e.g., reducing size of a tumor), inhibiting the growth rate of a cancer, and ameliorating or improving a clinical symptom or indicator associated with a cancer (such as tissue or serum components) or increasing longevity of the subject.
• the anti-cancer agent suitable for use in the methods described herein include any anti-cancer agents that have been approved for the treatment of cancer.
• the anti-cancer agent includes, but is not limited to, a targeted antibody, an angiogenisis inhibitor, an alkylating agent, an antimetabolite, a vinca alkaloid, a taxane, a podophyllotoxin, a topoisomerase inhibitor, a hormonal antineoplastic agent and other antineoplastic agents.
• the anti-cancer agents that can be used in methods described herein include, but are not limited to, paclitaxel, docetaxel, 5-fluorouracil, trastuzumab, lapatinib, bevacizumab, letrozole, goserelin, tamoxifen, cetuximab, panitumumab, gemcitabine, capecitabine, irinotecan, oxaliplatin, carboplatin, cisplatin, doxorubicin, epirubicin, cyclophosphamide, methotrexate, vinblastine, vincristine, melphalan, cytarabine, etoposide, daunorubicin, bleomycin, mitomycin and adriamycin and a combination thereof.
• anti-cancer drug is Venetoclax.
• anti cancer drug is 5-Azacytidine.
• Compound (I) and the additional therapeutic agent are administered concurrently or sequentially.
• Compound (I) and/or pharmaceutically acceptable salts thereof described herein are useful as an active pharmaceutical ingredients (API) as well as materials for preparing pharmaceutical compositions that incorporate one or more pharmaceutically acceptable excipients and is suitable for administration to human subjects.
• the disclosure provides a pharmaceutical composition
• a pharmaceutical composition comprising Compound (I) and/or a pharmaceutically acceptable salt thereof and at least one additional pharmaceutically acceptable excipient.
• pharmaceutically acceptable excipient refers to a pharmaceutically acceptable material, composition, and/or vehicle, such as a liquid or solid fdler, diluent, excipient, solvent, or encapsulating material. Each excipient must be “pharmaceutically acceptable” in the sense of being compatible with the subject composition and its components and not injurious to the patient.
• Some non-limiting examples of materials which may serve as pharmaceutically acceptable excipients include: (1) sugars, such as lactose, glucose, and sucrose; (2) starches, such as com starch and potato starch; (3) cellulose and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose, and cellulose acetate; (4) powdered tragacanth;
• oils such as peanut oil, cottonseed oil, safflower oil, sesame oil, olive oil, com oil, and soybean oil
• glycols such as propylene glycol
• polyols such as glycerin, sorbitol, mannitol, and polyethylene glycol
• esters such as ethyl oleate and ethyl laurate
• Remington The Science and Practice of Pharmacy, 21st edition, 2005, ed. D.B. Troy, Lippincott Williams & Wilkins, Philadelphia, and Encyclopedia of Pharmaceutical Technology, eds. J. Swarbrick and J. C. Boylan, 1988-1999, Marcel Dekker, New York, the contents of each of which is incorporated by reference herein, also disclose additional non- limiting examples of pharmaceutically acceptable excipients, as well as known techniques for preparing and using the same.
• the compounds used in the disclosed methods can be administered to a patient in a variety of forms depending on the selected route of administration, as will be understood by those skilled in the art.
• the compounds of the present teachings may be administered, for example, by oral, parenteral, buccal, sublingual, nasal, rectal, patch, pump or transdermal administration and the pharmaceutical compositions formulated accordingly.
• Parenteral administration includes intravenous, intraperitoneal, subcutaneous, intramuscular, transepithelial, nasal, intrapulmonary, intrathecal, rectal and topical modes of administration. Parenteral administration can be by continuous infusion over a selected period of time.
• the compounds used in the disclosed methods can be suitably formulated into pharmaceutical compositions for administration to a subject.
• compositions of the present teachings optionally include one or more pharmaceutically acceptable carriers and/or diluents therefor, such as lactose, starch, cellulose and dextrose.
• pharmaceutically acceptable carriers and/or diluents therefor such as lactose, starch, cellulose and dextrose.
• Other excipients such as flavoring agents; sweeteners; and preservatives, such as methyl, ethyl, propyl and butyl parabens, can also be included. More complete listings of suitable excipients can be found in the Handbook of Pharmaceutical Excipients (5 th Ed., Pharmaceutical Press (2005)). A person skilled in the art would know how to prepare formulations suitable for various types of administration routes.
• a compound used in the disclosed methods may be incorporated with excipient and used in the form of ingestible tablets, buccal tablets, troches, capsules, elixirs, suspensions, syrups, wafers, and the like.
• solutions of a compound used in the disclosed methods can generally be prepared in water suitably mixed with a surfactant such as hydroxypropylcellulose.
• Dispersions can also be prepared in glycerol, liquid polyethylene glycols, DMSO and mixtures thereof with or without alcohol, and in oils. Under ordinary conditions of storage and use, these preparations contain a preservative to prevent the growth of microorganisms.
• sterile aqueous solutions or dispersion of, and sterile powders of, a compound used in the disclosed methods for the extemporaneous preparation of sterile injectable solutions or dispersions are appropriate.
• Aerosol formulations typically comprise a solution or fine suspension of the active substance in a physiologically acceptable aqueous or non-aqueous solvent and are usually presented in single or multidose quantities in sterile form in a sealed container, which can take the form of a cartridge or refill for use with an atomizing device.
• the sealed container may be a unitary dispensing device such as a single dose nasal inhaler or an aerosol dispenser fitted with a metering valve which is intended for disposal after use.
• the dosage form comprises an aerosol dispenser, it will contain a propellant which can be a compressed gas such as compressed air or an organic propellant such as fluorochlorohydrocarbon.
• the aerosol dosage forms can also take the form of a pump-atomizer.
• the compounds used in the disclosed methods can be formulated with a carrier such as sugar, acacia, tragacanth, or gelatin and glycerine, as tablets, lozenges or pastilles.
• a carrier such as sugar, acacia, tragacanth, or gelatin and glycerine, as tablets, lozenges or pastilles.
• the compounds used in the disclosed methods can be formulated in the form of suppositories containing a conventional suppository base such as cocoa butter.
• Compound (I) was prepared as a 10 mM stock in 100% DMSO and diluted with RPMI 1640 cell growth medium containing 10% FBS such that the final concentrations ranged from 50 pM to 15 uM. Aliquots (20 uL) from each concentration were overlaid to 80 uL of pre-seeded cells to achieve final concentrations of 10 pM to 3 uM. After 3 days, cell viability in each well was assessed by alamarBlue assay according to the manufacturer's instruction (ThermoFisher Scientific).
• the human acute lymphoblastic leukemia cell line MOLT-4 was acquired from American Type Culture Collection (Manassas, VA, USA) and grown in RPMI medium containing 100 units/mL penicillin G sodium, 100 pg/mL streptomycin sulfate. The media was supplemented with 10% heat-inactivated fetal bovine serum, 2 mM L-glutamine, and 0.11% sodium pyruvate. The tumor cells were maintained in a humidified environment of 5% CO2 and 95% air at 37 °C. Cells were verified to be free of mouse pathogens by IMPACT IV PCR analysis (IDEXX RADIL, Colombia, MO, USA) before injection.
• mice Female SCID mice were purchased from the Ontario Cancer Institute and received and acclimated at the MaRS-TMDT Animal Resources Centre for 2 weeks prior to the start of the experiment. The mice were fed ad libitum autoclaved water and Rodent Lab Diet (Harlan Teklad LM-485) consisting of 19% crude protein, 5% crude fat, and 5% crude fiber. Mice were housed in microisolator cages and maintained in an environment with a 12-hour light cycle at 20-22 °C and 40-60% humidity.
• MOLT-4 cells were harvested and resuspended with serum free DMEM to a concentration of 1 x 10 8 /mL and each mouse was injected subcutaneously with a volume of 0.1 mL containing 1 x 10 7 MOLT-4 cells in the right rear flank.
• Toxicity was evaluated by body weight measurements and clinical observations.
• the average volume of the control tumors was 1754 mm 3 , averaging 683% tumor growth.
• tumors continued to regress, with maximum antitumor efficacy observed on Day 25, with 8 of 8 complete regressions in the daily dosing arm and 6 of 8 complete regressions in the 2-on/5-off arm (average 96% regression). Tumor regrowth eventually occurred in all animals, with the last animal taken off study due to excessive tumor burden on Day 68.
• FIG. 2 shows tumor volume (MOLT-4) in SCID mice vs treatment day.
• FIG. 3 shows the body weight (SCID mice) vs treatment day.
• Compound (I) is very efficacious and potentially curative in the MOLT-4 acute lymphoblastic leukemia xenograft model.
• Example 3 Compound (I) Fumarate Inhibits Tumor Growth in MV4-11 AML Model.
• the human acute myeloid leukemia cell line MV4-11 was acquired from American Type Culture Collection (Manassas, VA, USA) and grown in RPMI medium containing 100 units/mL penicillin G sodium, 100 pg/mL streptomycin sulfate. The media was supplemented with 10% heat-inactivated fetal bovine serum, 2 mM L-glutamine, and 0.11% sodium pyruvate. The tumor cells were maintained in a humidified environment of 5% CO2 and 95% air at 37°C. Cells were verified to be free of mouse pathogens by IMPACT IV PCR analysis (IDEXX RADIL, Colombia, MO, USA) before injection. [0080] Animals and tumor cells:
• mice Female SCID mice were purchased from the Ontario Cancer Institute and received and acclimated at the MaRS-TMDT Animal Resources Centre for 2 weeks prior to the start of the experiment. The mice were fed ad libitum autoclaved water and Rodent Lab Diet (Harlan Teklad LM-485) consisting of 19% crude protein, 5% crude fat, and 5% crude fiber. Mice were housed in microisolator cages and maintained in an environment with a 12-hour light cycle at 20-22°C and 40-60% humidity.
• MV4-11 cells were harvested and resuspended with serum free DMEM to a concentration of 1 x 10 8 /mL and each mouse was injected subcutaneously with a volume of 0.1 mL containing 1 x 10 7 MV4- 11 cells in the right rear flank.
• Toxicity was evaluated by body weight measurements and clinical observations.
• FIG. 4 shows tumor volume (MV4-11) in SCID mice vs treatment day.
• FIG. 5 shows the body weight (SCID mice) vs treatment day.
• Compound (I) is very efficacious and potentially curative in the MV4-11 acute myeloid leukemia xenograft model.
• Example 4 Phase 1 Study of Compound (I) Fumarate in Patients With Relapsed or Refractory Acute Myeloid Leukemia or Myelodysplastic Syndrome.
• NCT03187288 This study (NCT number: NCT03187288) is a multi-center, phase 1, dose- escalation trial designed to assess the safety, tolerability, pharmacokinetics, and clinical benefit of treatment with Compound (I) fiimarate administered orally over a range of doses in patients with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) that is relapsed or refractory to current treatment or for which no curative therapy exists.
• AML acute myeloid leukemia
• MDS myelodysplastic syndrome
• Results 9 patients with relapsed or refractory AML were treated with escalating doses of Compound (I) (64 mg to 128 mg) administered orally once daily. Among them, 3 patients were dosed at 64 mg, 4 patients were dosed at 96 mg, and 2 patients were dosed at 128 mg. More detailed information with respect to the patients is provided in the table below. Of six patients evaluable for response, two (33%) achieved complete remission (CR), and 3 patients (50%) had stable disease (with one patient having a 78% reduction in marrow blast count). The dose limiting toxicity (DLT) was determined to be colitis at the 128 mg dose level. The 96 mg dose level was suggested for fiirther exploration. However, only 4 patients were enrolled at the 96 mg dose level before the study was paused for enrollment and was amended.
• Compound (I) 64 mg to 128 mg
• 3 patients were dosed at 64 mg
• 4 patients were dosed at 96 mg
• 2 patients were dosed at 128 mg
• Example 5 Phase lb/2 Study of Compound (I) Fumarate as A Single Agent or in Combination With Azacitidine or Decitabine in Patients With Acute Myeloid Leukemia, Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia..
• the primary objectives of this study are (i) to assess the safety and tolerability, and identify the maximum tolerated dose (MTD) of Compound (I) administered orally in patients with acute myeloid leukemia (AML), Myelodysplastic Syndromes (MDS) or Chronic Myelomonocytic Leukemia (CMML); and (ii) to determine the Recommended Phase 2 Dose of Compound (I) in patients with AML, Myelodysplastic Syndromes (MDS) or Chronic Myelomonocytic Leukemia (CMML).
• MTD maximum tolerated dose
• the secondary objectives of this study are (i) to determine the PK of Compound (I) administered orally in patients with AML, Myelodysplastic Syndromes (MDS) or Chronic Myelomonocytic Leukemia (CMML); (ii) to determine the Composite Complete Remission Rate, CRc (complete remission + complete remission with incomplete blood count recovery + complete remission with incomplete platelet count recovery [CR + CRi + CRp]) of Compound (I) in patients with AML; and (iii) to determine the Overall Response Rate (ORR, defined as Complete remission + Marrow CR + Partial remission + Hematologic Improvement (CR + mCR+ PR + HI) in MDS or CMML.
• ORR Overall Response Rate
• Part 1A patients will receive oral Compound (I) daily, in the morning and in the absence of food, i.e. not eating for 2 h before or 1 h after taking their dose, for 21 days followed by 7 days off (28-day cycles), except on Day 1 and Day 21 of Cycle 1 when Compound (I) will be administered after an overnight fast. Water is permitted ad lib following 1 hour after the dose administration after the overnight fast; no food is allowed for at least 4 hours after the dose.
• the starting dose for Compound (I) is 32 mg and is based on preliminary clinical data.
• Patients who complete the initial cycle of therapy without evidence of significant toxicity or clinical evidence of progressive disease may receive additional 28- day cycles of treatment at the same dose level for up to 6 cycles and if no PR or better is achieved, the Investigator should remove the patient from study following discussion with the Medical Monitor.
• a bone marrow assessment will be performed after cycle 1, and after every cycle until a response (e.g., CR, CRi, CRp), and as clinically indicated.
• Patients achieving a CR should have a bone marrow examination every 3 months (approx. 12 weeks) for 1 year, then as clinically indicated.
• Treatment with Compound (I) may be delayed until recovery from the observed treatment-related toxicities and to consider if dose reductions are appropriate for continued therapy with Compound (I).
• a delay of up to 14 days is allowed for patients to return to baseline or grade 1 from any treatment -related side effects.
• the investigator, after discussion with the medical monitor may allow a patient to continue on study after a treatment delay of longer than 14 days if the patient is benefitting from the treatment and the treatment-related toxicities have returned to baseline or grade 1.
• Maximum Tolerated Dose and Dose Limiting Toxicities are defined below for the escalation portions of the study. Dose adjustments for toxicities occurring during the conduct of the study will be discussed in the protocol and generally will involve dose hold, reduction, and possibly discontinuation of study drug therapy depending on severity.
• Single agent dose optimization lead-in dose levels are defined below:
• the primary objectives of this study are (i) to further assess the safety and tolerability, and identify the maximum tolerated dose (MTD) of Compound (I) administered orally in patients with acute myeloid leukemia (AML), Myelodysplastic Syndromes (MDS) or Chronic Myelomonocytic Leukemia (CMML); and (ii) to evaluate the effect of food on pharmacokinetics of Compound (I) through oral administration of Compound (I) with/without a high fat meal in patients with AML, MDS or CMML.
• MTD maximum tolerated dose
• the secondary objectives of this study are (i) to determine the Composite Complete Remission Rate, CRc (complete remission + complete remission with incomplete blood count recovery + complete remission with incomplete platelet count recovery [CR + CRi + CRp]) of Compound (I) in patients with AML; and (ii) to determine the Overall Response Rate (ORR, defined as Complete remission + Marrow CR + Partial remission + Hematologic Improvement (CR + mCR+ PR + HI) in MDS or CMML.
• ORR Overall Response Rate
• Part IB patients will be administered oral Compound (I) daily at the proposed dose determined from Part 1A, for one week (study days 1-7), taking the drug in the morning and in the absence of food, i.e. not eating for 2 h before or 1 h after taking their dose for 21 days followed by 7 days off (28-day cycles), except on Day 1 and Day 21 of Cycle 1 when Compound (I) will be administered after an overnight fast.
• patients will be administered Compound (I) with 240 mL water and undergo post-dose PK sampling.
• a bone marrow assessment will be performed after cycle 1, and after every cycle until a response (e.g., CR, CRi, CRp), and as clinically indicated.
• Patients achieving a CR should have a bone marrow examination every 3 months (approx. 12 weeks) for 1 year, then as clinically indicated.
• Part 2 Dose Escalation for Combination Therapy Part 2A combination of Compound (I) and Azacitidine Part 2B combination of Compound (I) and Decitabine.
• the primary objectives of this study are (i) to assess the safety and tolerability, and identify the maximum tolerated dose (MTD) of Compound (I) administered orally in combination with azacitidine or decitabine in patients with AML or CMML; and (ii) to determine the Recommended Phase 2 Dose for the Combination Therapy (RP2D) of Compound (I) and azacitidine or Compound (I) and decitabine in patients with AML or MDS or CMML.
• MTD maximum tolerated dose
• R2D Recommended Phase 2 Dose for the Combination Therapy
• the secondary objectives of this study are (i) to determine the PK of Compound (I) administered orally in combination with azacitidine or decitabine in patients with AML or CMML; to determine the Composite Complete Remission Rate, CRc (complete remission + complete remission with incomplete blood count recovery + complete remission with incomplete platelet count recovery [CR + CRi + CRp]) of Compound (I) in patients with AML; and (iii) to determine the Overall Response Rate (ORR, defined as complete remission + Marrow CR + partial remission + Hematologic Improvement (CR + mCR+ PR + HI) in MDS or CMML.
• ORR Overall Response Rate
• a bone marrow assessment will be performed after cycle 1, and after every cycle until a response (e.g., CR, CRi, CRp), and as clinically indicated. Patients achieving a CR should have a bone marrow examination every 3 months (approx. 12 weeks) for 1 year, then as clinically indicated. [00115] Dose adjustments for toxicities occurring during the conduct of the study will be discussed in the protocol and generally will involve dose hold, reduction, and possibly discontinuation of study drug therapy depending on severity. Part 2A and 2B Dose escalation will proceed independently as illustrated below:

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