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SG11201911937UA - Amorphous and crystalline forms of ido inhibitors - Google Patents

Amorphous and crystalline forms of ido inhibitors

Info

Publication number
SG11201911937UA
SG11201911937UA SG11201911937UA SG11201911937UA SG11201911937UA SG 11201911937U A SG11201911937U A SG 11201911937UA SG 11201911937U A SG11201911937U A SG 11201911937UA SG 11201911937U A SG11201911937U A SG 11201911937UA SG 11201911937U A SG11201911937U A SG 11201911937UA
Authority
SG
Singapore
Prior art keywords
amorphous
crystalline forms
ido inhibitors
ido
inhibitors
Prior art date
Application number
SG11201911937UA
Inventor
Jay Powers
Hilary Beck
Maksim Osipov
Maureen Reilly
Hunter Shunatona
James Walker
Mikhail Zibinsky
Tamar Rosenbaum
Ian Young
Jennifer Nelson
Petinka Vlahova
Original Assignee
Bristol Myers Squibb Co
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 Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of SG11201911937UA publication Critical patent/SG11201911937UA/en

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
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • 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
    • A61K31/47Quinolines; Isoquinolines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/18Halogen atoms or nitro radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Quinoline Compounds (AREA)
SG11201911937UA 2017-06-30 2018-06-29 Amorphous and crystalline forms of ido inhibitors SG11201911937UA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201762527855P 2017-06-30 2017-06-30
PCT/US2018/040262 WO2019006283A1 (en) 2017-06-30 2018-06-29 Amorphous and crystalline forms of ido inhibitors

Publications (1)

Publication Number Publication Date
SG11201911937UA true SG11201911937UA (en) 2020-01-30

Family

ID=64742242

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201911937UA SG11201911937UA (en) 2017-06-30 2018-06-29 Amorphous and crystalline forms of ido inhibitors

Country Status (13)

Country Link
US (2) US11236049B2 (en)
EP (1) EP3644993B1 (en)
JP (1) JP7690284B2 (en)
KR (1) KR102630575B1 (en)
CN (1) CN111093651B (en)
AU (1) AU2018294314B2 (en)
BR (1) BR112019027259A2 (en)
CA (1) CA3066789A1 (en)
EA (1) EA202090119A1 (en)
IL (1) IL271601B2 (en)
MX (2) MX391848B (en)
SG (1) SG11201911937UA (en)
WO (1) WO2019006283A1 (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX383313B (en) * 2017-06-30 2025-03-13 Bristol Myers Squibb Co Substituted quinolinycyclohexylpropanamide compounds and improved methods for their preparation
CN115278855A (en) * 2017-11-17 2022-11-01 瑞典爱立信有限公司 Signaling TA offsets in NR
CN110357813A (en) * 2018-04-09 2019-10-22 信达生物制药(苏州)有限公司 A kind of new indole amine 2,3- dioxygenase inhibitor and its preparation method and application
WO2020000236A1 (en) * 2018-06-27 2020-01-02 深圳仁泰医药科技有限公司 Crystal form of (r)-n-(4-chlorophenyl)-2-(cis-4-(6-fluoroquinolin-4-yl)cyclohexyl) propionamide
EP4027980A1 (en) * 2019-09-11 2022-07-20 Bristol-Myers Squibb Company Pharmaceutical formulations of indoleamine 2, 3-dioxygenase inhibitors
CA3159071A1 (en) * 2019-11-26 2021-06-03 Tamar I. ROSENBAUM Salts/cocrystals of (r)-n-(4-chlorophenyl)-2-((1s,4s)-4-(6-fluoroquinolin-4-yl)cyclohexyl)propanamide
AR120935A1 (en) * 2020-01-02 2022-03-30 Hutchison Medipharma Ltd AMIDE DERIVATIVES AND USES THEREOF

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TWI309240B (en) 2004-09-17 2009-05-01 Hoffmann La Roche Anti-ox40l antibodies
EP1866339B8 (en) 2005-03-25 2021-12-01 GITR, Inc. Gitr binding molecules and uses therefor
ME02461B (en) 2005-05-10 2017-02-20 Incyte Holdings Corp INDOLEAMINE 2,3-DIOXYGENASE MODULATORS AND METHODS FOR THE USE OF THE SAME
KR101607288B1 (en) 2005-07-01 2016-04-05 이. 알. 스퀴부 앤드 선즈, 엘.엘.씨. Human monoclonal antibodies to programmed death ligand 1(pd-l1)
EP1971583B1 (en) 2005-12-20 2015-03-25 Incyte Corporation N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
CL2007002650A1 (en) 2006-09-19 2008-02-08 Incyte Corp COMPOUNDS DERIVED FROM HETEROCICLO N-HIDROXIAMINO; PHARMACEUTICAL COMPOSITION, USEFUL TO TREAT CANCER, VIRAL INFECTIONS AND NEURODEGENERATIVE DISORDERS BETWEEN OTHERS.
US20080125470A1 (en) 2006-09-19 2008-05-29 Incyte Corporation N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
EP1987839A1 (en) 2007-04-30 2008-11-05 I.N.S.E.R.M. Institut National de la Sante et de la Recherche Medicale Cytotoxic anti-LAG-3 monoclonal antibody and its use in the treatment or prevention of organ transplant rejection and autoimmune disease
EP2175884B8 (en) 2007-07-12 2017-02-22 GITR, Inc. Combination therapies employing gitr binding molecules
EP2044949A1 (en) 2007-10-05 2009-04-08 Immutep Use of recombinant lag-3 or the derivatives thereof for eliciting monocyte immune response
EP2227233B1 (en) 2007-11-30 2013-02-13 Newlink Genetics Ido inhibitors
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TWI729512B (en) 2008-12-09 2021-06-01 美商建南德克公司 Anti-pd-l1 antibodies and their use to enhance t-cell function
CN102574924A (en) 2009-09-03 2012-07-11 先灵公司 Anti-gitr antibodies
EP2493862B1 (en) 2009-10-28 2016-10-05 Newlink Genetics Corporation Imidazole derivatives as ido inhibitors
PT2949670T (en) 2009-12-10 2019-05-20 Hoffmann La Roche Antibodies binding preferentially human csf1r extracellular domain 4 and their use
NZ705128A (en) 2010-03-04 2015-04-24 Macrogenics Inc Antibodies reactive with b7-h3, immunologically active fragments thereof and uses thereof
WO2011107553A1 (en) 2010-03-05 2011-09-09 F. Hoffmann-La Roche Ag Antibodies against human csf-1r and uses thereof
CA2789071C (en) 2010-03-05 2018-03-27 F. Hoffmann-La Roche Ag Antibodies against human csf-1r and uses thereof
CN107011438B (en) 2010-05-04 2020-11-20 戊瑞治疗有限公司 Antibodies that bind CSF1R
SG10201912092VA (en) 2010-09-09 2020-02-27 Pfizer 4-1bb binding molecules
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DK2699264T3 (en) 2011-04-20 2018-06-25 Medimmune Llc ANTIBODIES AND OTHER MOLECULES BINDING B7-H1 AND PD-1
KR101981873B1 (en) 2011-11-28 2019-05-23 메르크 파텐트 게엠베하 Anti-pd-l1 antibodies and uses thereof
RU2658603C2 (en) 2011-12-15 2018-06-21 Ф.Хоффманн-Ля Рош Аг Antibodies against human csf-1r and uses thereof
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AR090263A1 (en) 2012-03-08 2014-10-29 Hoffmann La Roche COMBINED ANTIBODY THERAPY AGAINST HUMAN CSF-1R AND USES OF THE SAME
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UY34887A (en) 2012-07-02 2013-12-31 Bristol Myers Squibb Company Una Corporacion Del Estado De Delaware OPTIMIZATION OF ANTIBODIES THAT FIX THE LYMPHOCYTE ACTIVATION GEN 3 (LAG-3) AND ITS USES
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UY36390A (en) * 2014-11-05 2016-06-01 Flexus Biosciences Inc MODULATING COMPOUNDS OF INDOLAMINE ENZYME 2,3-DIOXYGENASE (IDO), ITS SYNTHESIS METHODS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
UY36391A (en) 2014-11-05 2016-06-01 Flexus Biosciences Inc MODULATING COMPOUNDS OF INDOLAMINE ENZYME 2,3-DIOXYGENASE (IDO1), ITS SYNTHESIS METHODS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
MX383313B (en) * 2017-06-30 2025-03-13 Bristol Myers Squibb Co Substituted quinolinycyclohexylpropanamide compounds and improved methods for their preparation

Also Published As

Publication number Publication date
US20200115342A1 (en) 2020-04-16
IL271601B2 (en) 2024-05-01
BR112019027259A2 (en) 2020-07-14
AU2018294314B2 (en) 2024-09-19
JP7690284B2 (en) 2025-06-10
MX2019014885A (en) 2020-02-13
CN111093651A (en) 2020-05-01
WO2019006283A1 (en) 2019-01-03
US20220169615A1 (en) 2022-06-02
KR102630575B1 (en) 2024-01-29
US12421195B2 (en) 2025-09-23
EP3644993A4 (en) 2021-03-10
MX391848B (en) 2025-03-19
AU2018294314A1 (en) 2020-02-06
IL271601B1 (en) 2024-01-01
EP3644993A1 (en) 2020-05-06
US11236049B2 (en) 2022-02-01
JP2020526520A (en) 2020-08-31
CN111093651B (en) 2023-06-06
KR20200020916A (en) 2020-02-26
IL271601A (en) 2020-02-27
CA3066789A1 (en) 2019-01-03
EP3644993B1 (en) 2023-08-02
MX2021015656A (en) 2022-02-03
EA202090119A1 (en) 2020-04-21

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