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
  • A61K31/66—Phosphorus compounds
  • A61K31/665—Phosphorus compounds having oxygen as a ring hetero atom, e.g. fosfomycin
• • 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
  • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
  • A61K31/337—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
• • 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
  • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
  • A61K31/365—Lactones
• • 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
  • 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
• • 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
  • 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

• Triptolide is a diterpene that has been shown to inhibit tumor cell proliferation and induce apoptosis in vitro and in animal models of cancer, including human mammary tumors (Shamon et al., Cancer Lett.1997;112:113-7), cholangio- carcinoma cells (Tengchaisri et al., Cancer Lett.1998;133:169–75), xenografts of several different tumor types, including melanoma, breast cancer, bladder cancer, gastric carcinoma (Yang et al., Mol Cancer Ther.2003;2:65-72), pancreatic tumors (Phillips et al., Cancer Res.
• triptolide is the result of inhibition of heat shock protein (HSP)70 expression in tumor cells and induction of apoptosis.
• HSP heat shock protein
• cytochrome c release from mitochondria into the cytosol and caspase-3 activity were significantly increased after incubation with triptolide (TPL), suggesting that the mitochondrial apoptotic pathway is responsible for TPL-induced cell death in these cells (Phillips et al., Cancer Res.2007;67(19):9407-16).
• TPL triptolide
• inhibition of HSP70 in the pancreatic tumors by TPL was mediated by inhibition of transcriptional activity of specificity protein 1 (Sp1) by TPL (Banerjee et al., Biol Chem.2013 Nov 22;288(47)).
• Sp1 is a transcription factor that regulates a number of pro-survival pathways like nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kB) and Heat shock factor 1 (HSF1). Inhibition of Sp1 transcriptional ability downregulates NF-kB activity thereby increasing apoptosis. Further, studies showed that activation of HSF1 (the key transcription factor for HSP70) was also regulated via Sp1 and NF-kB activity. 1 585.002WO1 Minneamrita Therapeutics Along with affecting the tumor cells, minnelide also depleted the extracellular matrix (ECM) of the pancreatic tumors by downregulating hyaluronan (HA) synthesis and preventing collagen cross linking.
• ECM extracellular matrix
• HA hyaluronan
• TPL induces autophagic cell death in some tumor types: the metastatic lines S2-013, S2-VP10 and Hs766T.
• TPL-induced autophagy requires autophagy-specific genes (atg5 or beclin1) and is associated with inactivation of the protein kinase B (Akt)/mammalian target of rapamycin/p70S6K pathway and up-regulation of the extracellular signal-related kinase (ERK) 1/2 pathway.
• Akt protein kinase B
• ERK extracellular signal-related kinase 1/2 pathway.
• TGF ⁇ transforming growth factor - ⁇
• CAFs cancer associated fibroblasts
• SE super-enhancers
• TPL cytotoxic to both pancreatic tumor cells and CAFs, disrupted SEs in a manner that resulted in the downregulation of SE-associated genes (e.g., BRD4, MYC, RNA Pol II, and Collagen 1) in both cell types at mRNA and protein levels.
• SE-associated genes e.g., BRD4, MYC, RNA Pol II, and Collagen 1
• TPL acts as an SE interactive agent and may elicit its antitumor activity through SE disruption to reprogram cellular cross talk and signaling in PDAC.
• epigenetic reprogramming of transcriptional regulation using SE modulating compounds such as TPL may provide means for effective treatment options for pancreatic cancer patients.
• this disclosure provides a method for treating pancreatic cancer in a cancer subject, the method which comprises administering to the cancer patient during a 28 day cycle a therapeutically effective combination of: a) about 0.25 mg to about 2.0 mg of minnelide according to a first regimen wherein a dose is given once per day on days 1 to 5, 8 to 12, and 15 to 19 of the cycle; b) about 75 mg/m 2 to about 125 mg/m 2 of nab-paclitaxel according to a second regimen wherein a dose is given once per day on days 1, 8, and 15 of the cycle; and c) about 600 mg/m 2 to about 1000 mg/m 2 of gemcitabine according to the second regimen of the cycle; wherein the cycle is repeated one or more times and the combination effectively treats the pancreatic cancer.
• the described technology provides for the use of the compositions described herein for use in medical therapy.
• the medical therapy can be treating cancer, for example, breast cancer, gastric cancer, lung cancer, pancreatic cancer, prostate cancer, or colon cancer.
• the invention also provides for the use of a composition as described herein for the manufacture of a medicament to treat a disease in a mammal, for example, cancer in a human.
• the medicament can include a pharmaceutically acceptable diluent, excipient, or carrier.
• FIG. 1A-B Mean tumor volumes (A) and tumor weights (B) 28 days after initiation of once daily po treatment with gemcitabine/abraxane with or without minnelide in an orthotopic S2-VP10 pancreatic tumor model.
• DETAILED DESCRIPTION A preclinical study of minnelide was conducted in mice.
• mice Female athymic nude mice (NCI nu/nu; 4 to 6 weeks old) were anesthetized with xylazine/ketamine, and S2-VP10 tumor cells embedded in Matrigel were implanted into the pancreatic tail (3 x 105 cells/mouse). Twelve days after tumor implantation (Day 0), animals were randomized to receive saline, nab-paclitaxel plus gemcitabine (Gem/Abx; 250/25 mg/kg), or minnelide plus nab-paclitaxel plus gemcitabine (Minn/Gem/Abx; 0.15/250/25 mg/kg or 0.21/250/25 mg/kg) (10 animals/group).
• Minnelide was administered once daily (QD) by oral gavage (PO). Treatment continued until Day 28 when animals were sacrificed. Treatment with Gem/Abx resulted in reduced tumor volumes and weights on Day 28 compared with saline-treated (vehicle) controls. The addition of minnelide at a dose of 0.15 mg/kg or 0.21 mg/kg further reduced tumor volumes and weights compared with Gem/Abx treatment alone ( Figure 1). Overall, daily oral treatment with minnelide decreased tumor volumes and weights when administered concurrently with Gem/Abx treatment compared with minnelide or Gem/Abx treatment alone in the orthotopic S2-VP10 pancreatic tumor model. Additional information and data supporting the invention can be found in U.S.
• a reference to "a compound” includes a plurality of such compounds, so that a compound X includes a plurality of compounds X.
• the claims may be drafted to exclude any optional element. As such, this statement is intended to serve as antecedent basis for the use of exclusive terminology, such as “solely,” “only,” and the like, in connection with any element described herein, and/or the recitation of claim elements or use of “negative” limitations.
• the term “and/or” means any one of the items, any combination of the items, or all of the items with which this term is associated.
• the phrases “one or more” and “at least one” are readily understood by one of skill in the art, particularly when read in context of its usage.
• the phrase can mean one, two, three, four, five, six, ten, 100, or any upper limit approximately 10, 100, or 1000 times higher than a recited lower limit.
• one or more substituents on a phenyl ring refers to one to five, or one to four, for example if the phenyl ring is disubstituted.
• all numbers, including those expressing quantities of ingredients, properties such as molecular weight, reaction conditions, and so forth, are approximations and are understood as being optionally modified in all instances by the term "about.” These values can vary depending upon the desired properties sought to be obtained by those skilled in the art utilizing the teachings of the descriptions herein.
• the term “about” can include one or two integers greater than and/or less than a recited integer at each end of the range. Unless indicated otherwise herein, the terms “about” and “approximately” are intended to include values, e.g., weight percentages, proximate to the recited range that are equivalent in terms of the functionality of the individual ingredient, composition, or embodiment. The terms “about” and “approximately” can also modify the endpoints of a recited range as discussed above in this paragraph.
• ranges recited herein also encompass any and all possible sub-ranges and combinations of sub-ranges thereof, as well as the individual values making up the range, particularly integer values. It is therefore understood that each unit between two particular units are also disclosed. For example, if 10 to 15 is disclosed, then 11, 12, 13, and 14 are also disclosed, individually, and as part of a range.
• a recited range e.g., weight percentages or carbon groups
• any listed range can be easily recognized as sufficiently describing and enabling the same range being broken down into at least equal halves, thirds, quarters, fifths, or tenths.
• each range discussed herein can be readily broken down into a lower third, middle third and upper third, etc.
• all language such as “up to”, “at least”, “greater than”, “less than”, “more than”, “or more”, and the like include the number recited and such terms refer to ranges that can be subsequently broken down into sub-ranges as discussed above.
• all ratios recited herein also include all sub-ratios falling within the broader ratio. Accordingly, specific values recited for radicals, substituents, and ranges, are for illustration only; they do not exclude other defined values or other values within defined ranges for radicals and substituents.
• each of the ranges are significant both in relation to the other endpoint, and independently of the other endpoint.
• This disclosure provides ranges, limits, and deviations to variables such as volume, mass, percentages, ratios, etc. It is understood by an ordinary person skilled in the art that a range, such as “number1” to “number2”, implies a continuous range of numbers that includes the whole numbers and fractional numbers. For example, 1 to 10 means 1, 2, 3, 4, 5, ... 9, 10. It also means 1.0, 1.1, 1.2.1.3, ..., 9.8, 9.9, 10.0, and also means 1.01, 1.02, 1.03, and so on.
• variable disclosed is a number less than “number10”, it implies a continuous range that includes whole numbers and fractional numbers less than number10, as discussed above.
• variable disclosed is a number greater than “number10”
• 6 585.002WO1 Minneamrita Therapeutics includes whole numbers and fractional numbers greater than number10.
• contacting refers to the act of touching, making contact, or of bringing to immediate or close proximity, including at the cellular or molecular level, for example, to bring about a physiological reaction, a chemical reaction, or a physical change, e.g., in a solution, in a reaction mixture, in vitro, or in vivo.
• An "effective amount” refers to an amount effective to treat a disease, disorder, and/or condition, or to bring about a recited effect.
• an effective amount can be an amount effective to reduce the progression or severity of the condition or symptoms being treated. Determination of a therapeutically effective amount is well within the capacity of persons skilled in the art.
• an “effective amount” is intended to include an amount of a compound described herein, or an amount of a combination of compounds described herein, e.g., that is effective to treat or prevent a disease or disorder, or to treat the symptoms of the disease or disorder, in a host.
• an “effective amount” generally means an amount that provides the desired effect.
• the terms "effective amount” or “therapeutically effective amount,” as used herein, refer to a sufficient amount of an agent or a composition or combination of compositions being administered which will relieve to some extent one or more of the symptoms of the disease or condition being treated. The result can be reduction and/or alleviation of the signs, symptoms, or causes of a disease, or any other desired alteration of a biological system.
• an "effective amount” for therapeutic uses is the amount of the composition comprising a compound as disclosed herein required to provide a clinically significant decrease in disease symptoms.
• An appropriate "effective" amount in any individual case may be determined using techniques, such 7 585.002WO1 Minneamrita Therapeutics as a dose escalation study. The dose could be administered in one or more administrations. However, the precise determination of what would be considered an effective dose may be based on factors individual to each patient, including, but not limited to, the patient's age, size, type or extent of disease, stage of the disease, route of administration of the compositions, the type or extent of supplemental therapy used, ongoing disease process and type of treatment desired (e.g., aggressive vs. conventional treatment).
• treating include (i) preventing a disease, pathologic or medical condition from occurring (e.g., prophylaxis); (ii) inhibiting the disease, pathologic or medical condition or arresting its development; (iii) relieving the disease, pathologic or medical condition; and/or (iv) diminishing symptoms associated with the disease, pathologic or medical condition.
• the terms “treat”, “treatment”, and “treating” can extend to prophylaxis and can include prevent, prevention, preventing, lowering, stopping or reversing the progression or severity of the condition or symptoms being treated.
• treatment can include medical, therapeutic, and/or prophylactic administration, as appropriate.
• subject or “patient” means an individual having symptoms of, or at risk for, a disease or other malignancy.
• a patient may be human or non-human and may include, for example, animal strains or species used as “model systems” for research purposes, such a mouse model as described herein.
• the patient may include either adults or juveniles (e.g., children).
• patient may mean any living organism, preferably a mammal (e.g., human or non-human) that may benefit from the administration of compositions contemplated herein.
• mammals include, but are not limited to, any member of the Mammalian class: humans, non-human primates such as chimpanzees, and other apes and monkey species; farm animals such as cattle, horses, sheep, goats, swine; domestic animals such as rabbits, dogs, and cats; laboratory animals including rodents, such as rats, mice and guinea pigs, and the like.
• non-mammals include, but are not limited to, birds, fish and the like.
• the mammal is a human.
• the terms “providing”, “administering,” “introducing,” are used interchangeably herein and refer to the placement of a compound of the disclosure into a subject by a method or route that results in at least partial localization of the compound to a desired site.
• the compound can be administered by any appropriate route that results in delivery to a desired location in the subject.
• the compound and compositions described herein may be administered with additional compositions to prolong stability and activity of the compositions, or in combination with other therapeutic drugs.
• the terms “inhibit”, “inhibiting”, and “inhibition” refer to the slowing, halting, or reversing the growth or progression of a disease, infection, condition, or group of cells.
• the inhibition can be greater than about 20%, 40%, 60%, 80%, 90%, 95%, or 99%, for example, compared to the growth or progression that occurs in the absence of the treatment or contacting.
• the term “substantially” as used herein, is a broad term and is used in its ordinary sense, including, without limitation, being largely but not necessarily wholly that which is specified.
• the term could refer to a numerical value that may not be 100% the full numerical value.
• the full numerical value may be less by about 1%, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, about 10%, about 15%, or about 20%.
• adverse event refers to any untoward medical occurrence associated with the use of a drug in humans, whether or not considered drug related.
• serious adverse event refers to death, a life-threatening adverse event, inpatient hospitalization or prolongation of existing hospitalization, a persistent or significant incapacity or substantial disruption of the ability to conduct normal life functions, or a congenital anomaly/birth defect.
• Important medical events that may not result in death, be life-threatening, or require hospitalization may be considered serious when, such medical events include allergic bronchospasm requiring intensive treatment in an emergency room or at home, blood dyscrasias or convulsions that do not result in inpatient hospitalization, or the development of drug dependency or drug abuse, etc.
• the term “regimen” refers to a course of medical treatment over a period of time.
• the regimen described herein includes one or more sub-regimens, such as a first regimen, a second regime, and so on, that make up the entire regimen of medical treatment.
• the period of time for treatment may be one or more days, one or more weeks, one or more months, etc., wherein the 9 585.002WO1 Minneamrita Therapeutics period of time may be repeated in a cyclic fashion one or more times.
• a period of time may be 28 days, defining the length of a cycle that may be repeated.
• a regimen may be a 28 day cycle where a compound A is administered on specific days of the cycle, defining a first regimen, and where compound B is administered on other specific days of the cycle that define a second regimen, which in total defines the entire regimen.
• the IUPAC chemical name for the compound MINNELIDE or Minnelide TM is: disodium;[(1S,2S,4S,5S,7S,8R,9R,11S,13S)-1-methyl-17-oxo-7-propan-2-yl-3,6,10,16- tetraoxaheptacyclo[11.7.0.0 2,4 .0 2,9 .0 5,7 .0 9,11 .0 14,18 ]icos-14(18)-en-8-yl]oxymethyl phosphate.
• MINNELIDE and other pharmaceutically acceptable salt forms thereof will be referred to as compound 1. Classification of Adverse Events by Severity.
• AE Adverse Event
• NCI CTCAE National Cancer Institute Common Terminology Criteria for Adverse Events
• Grade 1 An AE that is transient or mild discomfort, not interfering with the patient’s daily activity performance or functioning; medical intervention/therapy may be required.
• Grade 2 An AE of sufficient severity as to possibly make the patient moderately uncomfortable; possibly influencing the patient’s daily activity performance or functioning; generally, not impairing the patient’s ability to continue in the study; and/or possibly needing therapeutic intervention.
• Grade 3 An AE event generally causing severe discomfort, significantly influencing the patient’s daily activity performance or functioning, generally requiring alteration or cessation of study drug administration, and/or generally requiring therapeutic intervention with hospitalization possible.
• This disclosure provides a method for treating cancer in a cancer subject, the method which comprises administering to the cancer patient during a 28 day cycle a therapeutically effective combination of: 10 585.002WO1 Minneamrita Therapeutics a) about 0.25 mg to about 2.0 mg of minnelide according to a first regimen wherein a dose is given once per day on days 1 to 5, 8 to 12, and 15 to 19 of the cycle; b) about 75 mg/m 2 to about 125 mg/m 2 of nab-paclitaxel according to a second regimen wherein a dose is given once per day on days 1, 8, and 15 of the cycle; and c) about 600 mg/m 2 to about 1000 mg/m 2 of gemcitabine according to the second regimen of the cycle; wherein the cycle is repeated one or more
• the cancer subject is administered about 0.25 mg to about 1.00 mg of minnelide according to the first regimen.
• the cancer subject is administered a milligram amount of minnelide that is about 0.15 mg, 0.25 mg, 0.35 mg, 0.4 mg, 0.5 mg, 0.6 mg, 0.7 mg, 0.8 mg, 0.9 mg, 1.0 mg, 1.1 mg, 1.2 mg, 1.3 mg, 1.4 mg, 1.5 mg, 1.6 mg, 1.7 mg, 1.8 mg, 1.9 mg, 2.0 mg, 2.2 mg, 2.3 mg, 2.4 mg, 2.5 mg, 2.6 mg, 2.7 mg, 2.8 mg, 2.9 mg, 3.0 mg, 3.5 mg, 4.0 mg, 4.5 mg, 5.0 mg, 5.5 mg, or about 6.0 mg.
• the cancer subject is administered about 50 mg/m 2 to about 100 mg/m 2 of paclitaxel according to the second regimen.
• the cancer subject is administered a milligram of paclitaxel that is about 5 mg/m 2 , 10 mg/m 2 , 15 mg/m 2 , 20 mg/m 2 , 25 mg/m 2 , 30 mg/m 2 , 35 mg/m 2 , 40 mg/m 2 , 45 mg/m 2 , 50 mg/m 2 , 55 mg/m 2 , 60 mg/m 2 , 65 mg/m 2 , 70 mg/m 2 , 75 mg/m 2 , 80 mg/m 2 , 85 mg/m 2 , 90 mg/m 2 , 95 mg/m 2 , 100 mg/m 2 , 125 mg/m 2 , 150 mg/m 2 , 175 mg/m 2 , or about 200 mg/m 2 .
• the cancer subject is administered about 0.25 mg of minnelide according to the first regimen, about 75 mg/m 2 of nab-paclitaxel and about 600 mg/m 2 of gemcitabine each according to the second regimen. In some embodiments, the cancer subject is administered about 0.25 mg of minnelide according to the first regimen, about 100 mg/m 2 of nab-paclitaxel and about 800 mg/m 2 of gemcitabine each according to the second regimen. In some embodiments, the cancer subject is administered about 0.25 mg of minnelide according to the first regimen, about 125 mg/m 2 of nab-paclitaxel and about 1000 mg/m 2 of gemcitabine each according to the second regimen.
• the cancer subject is administered about 0.50 mg of minnelide according to the first regimen, about 125 mg/m 2 of nab-paclitaxel and about 1000 mg/m 2 of gemcitabine each according to the second regimen.
• 11 585.002WO1 Minneamrita Therapeutics In some embodiments, the cancer subject is administered about 0.75 mg of minnelide according to the first regimen, about 125 mg/m 2 of nab-paclitaxel and about 1000 mg/m 2 of gemcitabine each according to the second regimen.
• the cancer subject is administered about 1.00 mg of minnelide according to the first regimen, about 125 mg/m 2 of nab-paclitaxel and about 1000 mg/m 2 of gemcitabine each according to the second regimen. In some embodiments, the cancer subject is administered about 1.25 mg of minnelide according to the first regimen, about 125 mg/m 2 of nab-paclitaxel and about 1000 mg/m 2 of gemcitabine each according to the second regimen. In some embodiments, the cancer subject is administered about 1.50 mg of minnelide according to the first regimen, about 125 mg/m 2 of nab-paclitaxel and about 1000 mg/m 2 of gemcitabine each according to the second regimen.
• the cancer subject is administered about 1.75 mg of minnelide according to the first regimen, about 125 mg/m 2 of nab-paclitaxel and about 1000 mg/m 2 of gemcitabine each according to the second regimen. In some embodiments, the cancer subject is administered about 2.00 mg of minnelide according to the first regimen, about 125 mg/m 2 of nab-paclitaxel and about 1000 mg/m 2 of gemcitabine each according to the second regimen. In some embodiments, the cancer subject is administered about 1.25 mg of minnelide according to the first regimen, about 125 mg/m 2 of nab-paclitaxel and about 1000 mg/m2 of gemcitabine each according to the second regimen.
• the cancer subject is administered about 1.50 mg of minnelide according to the first regimen, about 125 mg/m 2 of nab-paclitaxel and about 1000 mg/m 2 of gemcitabine each according to the second regimen. In some embodiments, the cancer subject is administered about 1.75mg of minnelide according to the first regimen, about 125 mg/m 2 of nab-paclitaxel and about 1000 mg/m 2 of gemcitabine each according to the second regimen. In some embodiments, the cancer subject is administered about 2.00 mg of minnelide according to the first regimen, about 125 mg/m 2 of nab-paclitaxel and about 1000 mg/m 2 of gemcitabine each according to the second regimen.
• minnelide is administered orally or . In some embodiments, minnelide is administered intravenously. In various embodiments, nab-paclitaxel is administered intravenously or orally. In various embodiments, gemcitabine is administered intravenously or orally. In various embodiments, nab-paclitaxel is administered intravenously, concurrently or 12 585.002WO1 Minneamrita Therapeutics sequentially with gemcitabine. In various embodiments, gemcitabine is administered intravenously, concurrently or sequentially, with nab-paclitaxel. In various embodiments, the cancer is gastric cancer, pancreatic cancer, ovarian cancer, breast cancer, bladder cancer, skin cancer, or a combination thereof.
• cancer is pancreatic cancer.
• the method effectively treats a cancer subject suffering from or further suffering from gastric cancer, pancreatic cancer, ovarian cancer, breast cancer, bladder cancer, skin cancer, or a combination thereof.
• the cancer subject is a human.
• the cancer subject is a female human or a male human.
• the combination effectively treats the cancer without causing a complete blood count of the cancer subject to lower by more than 25 %, 20 %, 15 %, 10 %, or 5 % from baseline.
• the combination effectively treats the cancer without causing a platelet count or an absolute neutrophil count in the cancer subject to lower by more than 25 %, 20 %, 15 %, 10 %, or 5 % from baseline.
• the methods described herein are used to treat a cancer that has become refractory, or to treat a cancer that is resistant or non-responsive to other methods of cancer treatment.
• the pancreatic cancer is a cancer that has become refractory, resistant or non-responsive to other methods of cancer treatment.
• the pancreatic cancer is metastatic adenocarcinoma of the pancreas. Clinical Experience. Intravenous Minnelide.
• the deaths that occurred during the study were found to be not related to the study drug and were found to be related to progression of the patient’s disease (pancreatic/gastric cancer).
• TEAE TEAE
• hypoalbuminemia anemia, hypoproteinemia, fatigue, neutropenia, leukopenia, thrombocytopenia, nausea, hypocalcemia, diarrhea, hyperphosphatemia, constipation, vomiting, hyponatremia, lymphopenia, abdominal pain, dehydration, hyperglycemia, peripheral edema, hypophosphatemia, and headache.
• a total of 32 patients had at least 1 AE that was considered related to the study drug.
• Adverse events of neutropenia grade 3 and 4 of short durations have been observed at all dose levels and were determined to be drug related. The neutropenia resolved within a couple of days of not receiving treatment.
• Neutropenic fever and neutropenic infection were observed in three patients and determined to be drug related. Anemia and thrombocytopenia Grade 3 and 4 were observed in 22% of the patients and determined to be drug related. Other side effects of any grade that were possibly related to the drug included nausea, vomiting, diarrhea, constipation, anorexia, stomatitis, cerebellar toxicity, embolism and dyspnea, which occurred in ⁇ 3% of the patients. Oral Minnelide. A Phase 1, Multi-Center, Open-Label, Dose-Escalation, Safety, Pharmacokinetic, and Pharmacodynamic Study of MinnelideTM Capsules given alone or in combination with protein-bound paclitaxel in patients with Advanced Solid Tumors.
• IP investigational product
• the combination regimen was put on enrolment hold until further escalation parameters were introduced.
• the second DLT occurred in the first patient of the 0.25 mg minnelide and 100 mg/m 2 protein-bound paclitaxel cohort: a Grade 5 event of sepsis.
• Five additional patients have been enrolled in the 0.25 mg minnelide and 100 mg/m 2 protein-bound paclitaxel cohort with no DLTs observed. Summary of Adverse Events.
• Dose-Limiting Toxicity Dose-limiting toxicities (DLT) were evaluated during Cycle 1 of treatment. Toxicities were graded and documented according to the NCI CTCAE guidelines (briefly defined above). Dose reductions were not allowed during Cycle 1.
• DLT Dose-limiting toxicities
• DLTs include adverse events that are considered to be related to the study drug, including: Grade 4 neutropenia lasting ⁇ 5 days, Grade 4 neutropenia with use of growth factor, or Grade 3 or 4 neutropenia with fever and/or infection; Grade 4 thrombocytopenia (or Grade 3 with bleeding); 15 585.002WO1 Minneamrita Therapeutics Grade 3 or 4 treatment-related non-hematological toxicity (Grade 3 nausea, vomiting or diarrhea that last > 72 hours despite maximal treatment constitutes a DLT; or a dosing delay of greater than 2 weeks due to a treatment-emergent AEs or related severe laboratory abnormalities.
• Inclusion Criteria for Study Eligibility A patient must meet the inclusion criteria listed below: ⁇ Signed, written IRB-approved informed consent.
• ⁇ Patients diagnosed with histologically confirmed metastatic adenocarcinoma of the pancreas combined with adenocarcinoma and adenosquamous are allowed, but pure adenosquamous patients are excluded. Tumor progression after receiving standard/approved chemotherapy or where there is no approved therapy.
• ⁇ Patient who has received prior or going to receive any killed vaccine including influenza, pneumococcal or COVID-19 during the study are allowed but any live vaccine like Herpes Zoster is not allowed.
• AST Aspartate aminotransferase
• SGOT serum glutamic oxaloacetic transaminase
• ALT serum glutamic pyruvic transaminase
• ALP alkaline phosphatase
• Albumin ⁇ 3.0 g/dL. 16 585.002WO1 Minneamrita
• Therapeutics ⁇ Acceptable renal function: Serum creatinine within normal limits, OR calculated creatinine clearance ⁇ 60 mL/min/1.73 m 2 for patients with creatinine levels above institutional normal.
• ⁇ Acceptable hematologic status ⁇ Baseline absolute neutrophil count (ANC) ⁇ 2000 cells/mm3. ⁇ Platelet count ⁇ 100,000 (plt/ mm 3 ). ⁇ Hemoglobin ⁇ 9 g/dL. ⁇ Urinalysis: No clinically significant abnormalities.
• Acceptable coagulation status ⁇ Prothrombin time (PT) ⁇ 1.5 times institutional ULN. ⁇ Partial thromboplastin time (PTT) ⁇ 1.5 times institutional ULN. ⁇ International normalized ratio (INR) ⁇ 1.5 ⁇ institutional ULN. ⁇ For men and women of childbearing potential, the use of effective contraceptive methods during the study.
• From last dose effective contraception is to be maintained as follows: ⁇ Men: 100 days from last dose of minnelide. ⁇ Women of childbearing potential: 6 months from last dose of minnelide. ⁇ For females, agree to the use of two physician-approved contraceptive methods (oral, injectable, or implantable hormonal contraceptive; tubal ligation; intra-uterine device; barrier contraceptive with spermicide; or vasectomised partner) while on study IP; and for 3 months following the last dose of IP. ⁇ Has negative serum pregnancy test ( ⁇ -hCG) result at Screening.
• MinnelideTM Capsules would not resume until the ANC level was ⁇ 1500 mm 3 or platelet was ⁇ 100,000 cells/mm 3 . 17 585.002WO1 Minneamrita Therapeutics
• the following Examples are intended to illustrate the above invention and should not be construed as to narrow its scope. One skilled in the art will readily recognize that the Examples suggest many other ways in which the invention could be practiced. It should be understood that numerous variations and modifications may be made while remaining within the scope of the invention.
• EXAMPLES Example 1. Treatment Regimen. Minnelide was administered orally once a day on Days 1 to 5, Days 8 to 12 and Days 15 to 19.
• Nab-paclitaxel (Abraxane) plus gemcitabine was administered weekly by IV administration for 3 weeks on Days 1, 8, and 15 as per the Table 1 dose-escalation schedule. One cycle will be equal to 28 days.
• Minnelide TM capsules were given with the patient in a fasting state. At the first dose level 3 patients were treated. If no patients experienced CTCAE Version 5.0 Grade 3 or greater toxicity after a minimum of 3 weeks of treatment, dose escalation proceeded to dose level 2. If a DLT was observed in 1 out of 3 patients at any dose level, up to an additional 3 patients were enrolled and treated at that dose level. If 2 patients at that dose level had DLTs, dosing was decreased by one-half.
• dose level 1 the preceding dose (dose level 1) was declared the maximum tolerated dose (MTD). If 1 or less of 6 patients had DLT, the dose level 2 was declared the MTD. Table 1. Dose Escalation Regimen.
• Dose Escalation Dose T L Mevel Nab-paclitaxel on Gemcitabine on Number of Level Minnelide Capsules days 1, 8, and 15 days 1, 8, and 15 Patients -1 0.25 mg 75 mg/m 2 600 mg/m 2 3+3 0 0.25 mg 100 mg/m 2 800 mg/m 2 3+3 1 0.25 mg 125 mg/m 2 1000 mg/m 2 3+3 2 0.50 mg 125 mg/m 2 1000 mg/m 2 3+3 3 0.75 mg 125 mg/m 2 1000 mg/m 2 3+3 4 1.00 mg 125 mg/m 2 1000 mg/m 2 3+3 a Additional dose levels beyond dose level 6 could proceed with minnelide 0.25 mg increments when supported by safety data.
• Target Lesions Response criteria for target lesions are shown in Table 2. All measurable lesions up to a maximum of two lesions per organ and five lesions in total, representative of all involved organs, were identified as target lesions and recorded and measured at baseline. Target lesions were selected on the basis of their size (lesions with the longest diameter) and were representative of all involved organs, as well as their suitability for reproducible repeated measurements. All measurements were recorded using calipers if clinically assessed.
• a sum of the diameters (longest for non-nodal lesions, short axis for nodal lesions) for all target lesions were calculated and reported as the baseline sum diameters, which were used as a reference to further characterize any objective tumor regression in the measurable dimension of the disease. If lymph nodes were included in the sum, only the short axis contributed. Table 2. Criteria for target lesions. Complete Response Disappearance of all target lesions. Any pathological lymph nodes (CR) (whether target or non-target) must have reduction in short axis to ⁇ 10 mm.
• CR pathological lymph nodes
• Partial Response At least a 30% decrease in the sum of the diameters of target lesions, taking (PR) as reference the baseline sum of diameters Progressive Disease At least a 20% increase in the sum of the LD of target lesions, taking as (PD) reference the smallest sum on study (this may include the baseline sum).
• the sum must also demonstrate an absolute increase of at least 5 mm Stable Disease Neither sufficient shrinkage to qualify for PR nor sufficient increase to (SD) qualify for PD While specific embodiments have been described above with reference to the disclosed embodiments and examples, such embodiments are only illustrative and do not limit the scope of the invention. Changes and modifications can be made in accordance with ordinary skill in the art without departing from the invention in its broader aspects as defined in the following claims.

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