WO2022067185A1 - Méthodes de traitement du cancer de la prostate à effets secondaires minimes - Google Patents

Méthodes de traitement du cancer de la prostate à effets secondaires minimes Download PDF

Info

Publication number
WO2022067185A1
WO2022067185A1 PCT/US2021/052209 US2021052209W WO2022067185A1 WO 2022067185 A1 WO2022067185 A1 WO 2022067185A1 US 2021052209 W US2021052209 W US 2021052209W WO 2022067185 A1 WO2022067185 A1 WO 2022067185A1
Authority
WO
WIPO (PCT)
Prior art keywords
compound
subject
day
prostate cancer
pharmaceutically acceptable
Prior art date
Application number
PCT/US2021/052209
Other languages
English (en)
Inventor
Mitchell Steiner
Gary K. BARNETTE
Robert Getzenberg
Domingo Rodriguez
Original Assignee
Veru Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Veru Inc. filed Critical Veru Inc.
Publication of WO2022067185A1 publication Critical patent/WO2022067185A1/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41781,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/28Compounds containing heavy metals
    • A61K31/29Antimony or bismuth compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/451Non condensed piperidines, e.g. piperocaine having a carbocyclic group directly attached to the heterocyclic ring, e.g. glutethimide, meperidine, loperamide, phencyclidine, piminodine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/08Drugs for disorders of the urinary system of the prostate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

Definitions

  • ADT androgen deprivation therapy
  • hematologic toxicities e.g., neutropenias including febrile neutropenias, thrombocytopenias, etc.
  • neurotoxicities e.g., neuropathies including peripheral neuropathy which
  • Another embodiment of the invention encompasses methods wherein the amount of Compound 17ya is any of about 4.5 mg, 9 mg, 14 mg, 18 mg, 23 mg, 27 mg, 32 mg, 36 mg, 41 mg, 45 mg, 54 mg, 63 mg, 72 mg, or 81 mg.
  • the dose is a daily dose.
  • An embodiment of the invention encompasses methods wherein the subject is dosed to yield an AUCinf of less than 1950 hr*ng/mL.
  • Another embodiment of the invention encompasses wherein the dose is oral and taken once, twice, or thrice daily.
  • the present invention maximizes drug delivery in a therapeutically effective window while concurrently increasing patient tolerance and minimizing undesirable side effects.
  • many of the anticipated side effects associated with prostate cancer treatment are absent, including neutropenia, neurotoxicity, and/or myelosuppression, while side effects associated with the drug delivery method are minimal to nonexistent based on the dose and/or dosage regimen.
  • the invention encompasses methods of treating a subject with prostate cancer by administering Compound 17ya to yield an AUCinf of about 61.9 hr*ng/mL to about 3342 hr*ng/mL, whereby the subject does not experience neutropenias, neurotoxicities, or gastrointestinal toxicities.
  • the method includes an AUCinf of about 140 hr*ng/mL to about 2506.5 hr*ng/mL.
  • the method yields an AUCinf of about 278.5 hr*ng/mL to about 2228 hr*ng/mL.
  • Suitable pharmaceutically-acceptable salts of amines of compounds used in the method of the invention may be prepared from an inorganic acid or from an organic acid.
  • examples of inorganic salts of amines are bisulfates, borates, bromides, chlorides, hemisulfates, hydrobromates, hydrochlorates, 2-hydroxyethylsulfonates (hydroxyethanesulfonates), iodates, iodides, isothionates, nitrates, persulfates, phosphate, sulfates, sulfamates, sulfanilates, sulfonic acids (alkylsulfonates, arylsulfonates, halogen substituted alkylsulfonates, halogen substituted arylsulfonates), sulfonates and thiocyanates.
  • organic salts of amines include, but are not limited to, aliphatic, cycloaliphatic, aromatic, araliphatic, heterocyclic, carboxylic and sulfonic classes of organic acids, examples of which are acetates, arginines, aspartates, ascorbates, adipates, anthranilates, algenates, alkane carboxylates, substituted alkane carboxylates, alginates, benzenesulfonates, benzoates, bisulfates, butyrates, bicarbonates, bitartrates, citrates, camphorates, camphorsulfonates, cyclohexylsulfamates, cyclopentanepropionates, calcium edetates, camsylates, carbonates, clavulanates, cinnamates, dicarboxylates, digluconates, dodecylsulfonates, dihydrochlorides, decanoates,
  • the salts may be formed by conventional means, such as by reacting the free base or free acid form of the product with one or more equivalents of the appropriate acid or base in a solvent or medium in which the salt is insoluble or in a solvent such as water, which is removed in vacuo or by freeze drying or by exchanging the ions of an existing salt for another ion or suitable ionexchange resin.
  • a maintenance dose of a compound, composition or formulation may be administered, if necessary. Subsequently, the dosage or frequency of administration, or both, may be reduced, as a function of the symptoms, to a level at which the improved condition is retained when the symptoms have been alleviated to the desired level. Subjects may, however, require intermittent treatment on a long-term basis upon any recurrence of disease symptoms.
  • the solid unit dosage forms can be of the conventional type.
  • the solid form can be a capsule and the like, such as an ordinary gelatin type containing the compounds and a carrier.
  • an estimated AUCinf (AUCo-24h or AUCo-t) was determined to be: 1671 hr*ng/mL for a dose of 54 mg of Compound 17ya; 1949 hr*ng/mL for a dose of 63 mg of Compound 17ya; and 2228 hr*ng/mL for a dose of 72 mg of Compound 17ya.
  • FIG. 4A illustrates a screening CT scan: the right anterior psoas muscle cancerous lymph node (1.7 cm X 1.5 cm).
  • Figure 4A illustrates a screening CT scan 8 months later: the right anterior psoas muscle cancerous lymph node (1.1 cm X 1.0 cm).
  • Figure 4B illustrates a coronal CT scan on day one of treatment (left panel) and after 15 months of treatment (right panel), which resulted in about - 33% growth (or 33% regression) of the tumor.

Landscapes

  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Urology & Nephrology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

La présente invention concerne des méthodes de traitement du cancer de la prostate par l'administration du Composé 17ya sans induire ou minimiser les effets secondaires indésirables.
PCT/US2021/052209 2020-09-27 2021-09-27 Méthodes de traitement du cancer de la prostate à effets secondaires minimes WO2022067185A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US202063083955P 2020-09-27 2020-09-27
US63/083,955 2020-09-27

Publications (1)

Publication Number Publication Date
WO2022067185A1 true WO2022067185A1 (fr) 2022-03-31

Family

ID=80846928

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2021/052209 WO2022067185A1 (fr) 2020-09-27 2021-09-27 Méthodes de traitement du cancer de la prostate à effets secondaires minimes

Country Status (1)

Country Link
WO (1) WO2022067185A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114805307A (zh) * 2022-04-29 2022-07-29 南京雷正医药科技有限公司 一种用于制备冠状病毒治疗药物的吲哚类化合物

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004056971A2 (fr) * 2002-12-19 2004-07-08 Genta Incorporated Methodes de traitement d'un trouble associe au bcl-2 a l'aide d'oligomeres anti-sens bcl-2
US20090181944A1 (en) * 2008-01-11 2009-07-16 John Frederick Boylan Method for cancer therapy
US20150374717A1 (en) * 2013-03-04 2015-12-31 Aventis Pharma S.A. Cabazitaxel and its use for treating metastatic prostate cancers
US20160015688A1 (en) * 2013-03-05 2016-01-21 University Of Tennessee Research Foundation Compounds for treatment of cancer
WO2016145298A1 (fr) * 2015-03-12 2016-09-15 The Regents Of The University Of California Méthodes de traitement du cancer par des inhibiteurs de ror gamma
US20180092930A1 (en) * 2016-09-30 2018-04-05 Janssen Pharmaceutica Nv Methods of diagnosing and treating abiraterone acetate- glucocorticoid -resistant or -sensitive metastatic castration resistant prostate cancer
WO2020157699A1 (fr) * 2019-01-30 2020-08-06 Aragon Pharmaceuticals, Inc. Anti-androgènes pour le traitement du cancer de la prostate métastatique sensible à la castration

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004056971A2 (fr) * 2002-12-19 2004-07-08 Genta Incorporated Methodes de traitement d'un trouble associe au bcl-2 a l'aide d'oligomeres anti-sens bcl-2
US20090181944A1 (en) * 2008-01-11 2009-07-16 John Frederick Boylan Method for cancer therapy
US20150374717A1 (en) * 2013-03-04 2015-12-31 Aventis Pharma S.A. Cabazitaxel and its use for treating metastatic prostate cancers
US20160015688A1 (en) * 2013-03-05 2016-01-21 University Of Tennessee Research Foundation Compounds for treatment of cancer
WO2016145298A1 (fr) * 2015-03-12 2016-09-15 The Regents Of The University Of California Méthodes de traitement du cancer par des inhibiteurs de ror gamma
US20180092930A1 (en) * 2016-09-30 2018-04-05 Janssen Pharmaceutica Nv Methods of diagnosing and treating abiraterone acetate- glucocorticoid -resistant or -sensitive metastatic castration resistant prostate cancer
WO2020157699A1 (fr) * 2019-01-30 2020-08-06 Aragon Pharmaceuticals, Inc. Anti-androgènes pour le traitement du cancer de la prostate métastatique sensible à la castration

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114805307A (zh) * 2022-04-29 2022-07-29 南京雷正医药科技有限公司 一种用于制备冠状病毒治疗药物的吲哚类化合物

Similar Documents

Publication Publication Date Title
AU2017334035B2 (en) Treatment of prostate cancer
JP6404242B2 (ja) がんの治療のための併用療法としてのエリブリンおよびレンバチニブの使用
KR20150017367A (ko) 종양 질환을 치료하기 위한 17-알파-히드록실라제 (c17,20-리아제) 억제제와 특이적 pi-3k 억제제의 조합물
JP2019505585A (ja) 2−ブロモ−1−(3,3−ジニトロアゼチジン−1−イル)エタノンの静脈内投与のための組成物および方法
EA024186B1 (ru) Применение кабазитаксела в комбинации с преднизоном или преднизолоном для лечения рака простаты
JP7169297B2 (ja) 再発膠芽腫(rgbm)の治療方法
KR20170007789A (ko) 퀴놀린 유도체로 갑상선암을 치료하기 위한 방법과 용도 및 갑상선암을 치료하기 위한 약학적 조성물
WO2020249602A1 (fr) Procédés de traitement de l'hypertension artérielle pulmonaire
WO2022067185A1 (fr) Méthodes de traitement du cancer de la prostate à effets secondaires minimes
JP4609877B2 (ja) 慢性拒絶反応抑制剤
US20210038578A1 (en) Method of treating cancer
US20160120871A1 (en) Pharmaceutical combinations of a pi3k inhibitor and a microtubule destabilizing agent
KR20240001121A (ko) 그렐린 저항성을 수반하는 악액질의 치료제 또는 예방제
JP2024510666A (ja) Ddr遺伝子変異転移性去勢感受性前立腺がんを処置するためのタラゾパリブおよび抗アンドロゲンの組合せ
JP2023509191A (ja) 癌を治療するための組み合わせ療法
WO2020053658A2 (fr) Solutions chimiothérapeutiques non aqueuses de dosage peroral
WO2009081837A1 (fr) Composition pharmaceutique utilisée pour atténuer les symptômes du tractus urinaire inférieur
WO2020205608A1 (fr) Utilisations d'antagonistes du récepteur des androgènes et d'inhibiteurs de la voie jnk et compositions pharmaceutiques associées
WO2021104319A1 (fr) Composition pharmaceutique combinée de dérivé de quinazoline ou de sel de celui-ci et son utilisation
TW202342051A (zh) 用於治療高風險轉移性激素敏感性前列腺癌之組合
CN112533600A (zh) 用于治疗小细胞肺癌的喹啉衍生物
WO2024074959A1 (fr) Combinaison de talazoparib et d'enzalutamide dans le traitement du cancer de la prostate résistant à la castration métastatique
US20060205795A1 (en) Cancer treatment with epothilones
WO2024098032A1 (fr) Utilisation de dianhydrogalactitol dans le traitement d'épendymomes
EP3682883A1 (fr) Dérivé de quinoléine pour le traitement de tumeurs neuroendocrines

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 21873598

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

32PN Ep: public notification in the ep bulletin as address of the adressee cannot be established

Free format text: NOTING OF LOSS OF RIGHTS PURSUANT TO RULE 112(1) EPC (EPO FORM 1205A DATED 02/08/2023)

122 Ep: pct application non-entry in european phase

Ref document number: 21873598

Country of ref document: EP

Kind code of ref document: A1