DK3180331T3 - Polymorfer af selinexor - Google Patents

Polymorfer af selinexor Download PDF

Info

Publication number
DK3180331T3
DK3180331T3 DK15754099.8T DK15754099T DK3180331T3 DK 3180331 T3 DK3180331 T3 DK 3180331T3 DK 15754099 T DK15754099 T DK 15754099T DK 3180331 T3 DK3180331 T3 DK 3180331T3
Authority
DK
Denmark
Prior art keywords
selinexor
polymorphs
Prior art date
Application number
DK15754099.8T
Other languages
Danish (da)
English (en)
Inventor
Brian Clinton Austad
David G Roe
Original Assignee
Karyopharm Therapeutics 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 Karyopharm Therapeutics Inc filed Critical Karyopharm Therapeutics Inc
Application granted granted Critical
Publication of DK3180331T3 publication Critical patent/DK3180331T3/da

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • A61K31/41961,2,4-Triazoles
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (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)
  • Plural Heterocyclic Compounds (AREA)
  • Medicinal Preparation (AREA)
DK15754099.8T 2014-08-15 2015-08-14 Polymorfer af selinexor DK3180331T3 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201462038069P 2014-08-15 2014-08-15
PCT/US2015/045395 WO2016025904A1 (en) 2014-08-15 2015-08-14 Polymorphs of selinexor

Publications (1)

Publication Number Publication Date
DK3180331T3 true DK3180331T3 (da) 2022-09-12

Family

ID=53969460

Family Applications (1)

Application Number Title Priority Date Filing Date
DK15754099.8T DK3180331T3 (da) 2014-08-15 2015-08-14 Polymorfer af selinexor

Country Status (18)

Country Link
US (6) US10519139B2 (cg-RX-API-DMAC7.html)
EP (2) EP3180331B1 (cg-RX-API-DMAC7.html)
JP (3) JP6777626B2 (cg-RX-API-DMAC7.html)
KR (1) KR102608259B1 (cg-RX-API-DMAC7.html)
CN (3) CN111484483B (cg-RX-API-DMAC7.html)
AU (4) AU2015301484B2 (cg-RX-API-DMAC7.html)
CA (1) CA2957266A1 (cg-RX-API-DMAC7.html)
CO (1) CO2017001884A2 (cg-RX-API-DMAC7.html)
DK (1) DK3180331T3 (cg-RX-API-DMAC7.html)
EA (1) EA201790384A1 (cg-RX-API-DMAC7.html)
ES (1) ES2926377T3 (cg-RX-API-DMAC7.html)
IL (1) IL250328B (cg-RX-API-DMAC7.html)
MA (1) MA40254B1 (cg-RX-API-DMAC7.html)
MX (2) MX388170B (cg-RX-API-DMAC7.html)
SG (2) SG11201700789SA (cg-RX-API-DMAC7.html)
UA (1) UA123535C2 (cg-RX-API-DMAC7.html)
WO (1) WO2016025904A1 (cg-RX-API-DMAC7.html)
ZA (1) ZA201700880B (cg-RX-API-DMAC7.html)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA115532C2 (uk) 2011-07-29 2017-11-27 Каріофарм Терапеутікс, Інк. Модулятори нуклеарного транспорту, що містять гідразид, і їхнє застосування
KR102163377B1 (ko) 2012-05-09 2020-10-08 바이오젠 엠에이 인코포레이티드 핵 수송 조절인자 및 이의 용도
EP2968278B8 (en) 2013-03-15 2019-05-22 Karyopharm Therapeutics Inc. Methods of promoting wound healing using crm1 inhibitors
AU2014284168B2 (en) 2013-06-21 2018-10-25 Karyopharm Therapeutics Inc. Nuclear transport modulators and uses thereof
WO2016025904A1 (en) 2014-08-15 2016-02-18 Karyopharm Therapeutics Inc. Polymorphs of selinexor
US10526295B2 (en) 2015-12-31 2020-01-07 Karyopharm Therapeutics Inc. Nuclear transport modulators and uses thereof
EP3397634A1 (en) 2015-12-31 2018-11-07 Karyopharm Therapeutics, Inc. Nuclear transport modulators and uses thereof
WO2017118940A1 (en) * 2016-01-08 2017-07-13 Dr. Reddy's Laboratories Limited Solid forms of selinexor and process for their preparation
US11602530B2 (en) 2016-11-28 2023-03-14 Biogen Ma Inc. CRM1 inhibitors for treating epilepsy
US10993943B2 (en) 2017-01-05 2021-05-04 Watson Laboratories Inc. Crystalline forms of selinexor and process for their preparation
CN106831731B (zh) * 2017-01-17 2019-11-08 广州市闻皓生物科技有限公司 一种Selinexor原料药的合成方法
WO2019232724A1 (en) * 2018-06-06 2019-12-12 Xw Laboratories, Inc. Compounds as nuclear transport modulators and uses thereof
WO2020072008A1 (en) * 2018-10-04 2020-04-09 Deva Holding Anonim Sirketi Novel solid dispersions of selinexor
CA3130107A1 (en) 2019-03-20 2020-09-24 Johnson Matthey Public Limited Company Co-crystal forms of selinexor
CN114040909B (zh) 2019-05-01 2025-06-03 卡尔约药物治疗公司 用于制备xpo1抑制剂以及用于制备xp01抑制剂的中间体的方法
EP3968987A4 (en) * 2019-05-16 2022-10-26 Mayo Foundation for Medical Education and Research METHODS AND MATERIALS FOR THE TREATMENT OF CANCER
EP3808742A1 (en) 2019-10-16 2021-04-21 Sandoz AG Polymorph of selinexor
US20230391754A1 (en) 2020-10-21 2023-12-07 Karyopharm Therapeutics Inc. Crystalline form of selinexor
CN112679477B (zh) * 2020-12-17 2021-10-26 佛山奕安赛医药科技有限公司 塞利尼索及其中间体的制备方法
EP4452525A1 (en) * 2021-12-20 2024-10-30 RTX Corporation Particle enhancement of ceramic matrix composites, method of manufacture thereof and articles comprising the same
CN116675677B (zh) * 2023-08-02 2023-09-26 中国林业科学研究院林产化学工业研究所 一种c8漆酚衍生物及其制备方法和应用

Family Cites Families (73)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1017398A (en) 1911-01-16 1912-02-13 John E Folsom Telegraph-key.
CS229934B2 (en) 1981-07-07 1984-07-16 Pfizer Production method subst.indolylacryte acid derivative
KR840000529A (ko) 1981-07-07 1984-02-25 콘스탄틴 루이스 클레멘트 인돌 유도체의 제조방법
US4778796A (en) 1985-07-19 1988-10-18 Dainippon Pharmaceutical Co., Ltd. ω-(3-pyridyl)alkenamide derivatives and anti-allergenic pharmaceutical compositions containing same
IL97249A (en) 1990-02-23 1995-01-24 Takeda Chemical Industries Ltd Compounds of 7,6,5,4-tetrahydrothiazole] B-5,4 [pyridine and compounds of 5,6-dihydro-H4-pyrrolo] D-3,2 [thiazole, their manufacture, and pharmaceutical compositions including or
JP3111321B2 (ja) 1990-02-23 2000-11-20 武田薬品工業株式会社 縮合チアゾール化合物
US5541213A (en) 1993-06-24 1996-07-30 Eisai Co., Ltd. Propenoic acid derivatives diazole propenoic acid compounds which have useful pharmaceutical utility
US5468353A (en) 1994-05-05 1995-11-21 Minnesota Mining And Manufacturing Company Mist suppressant for solvent extraction metal electrowinning
CA2205998C (en) 1994-11-23 2002-07-16 Neurogen Corporation Certain 4-aminomethyl-2-substituted imidazole derivatives and 2-aminomethyl-4-substituted imidazole derivatives; new classes of dopamine receptor subtype specific ligands
US20030018025A1 (en) 1995-06-07 2003-01-23 Neurogen Corporation, Corporation Of The State Of Delaware Certain 4-aminomethyl-2-substituted imidazole derivatives and 2-aminomethyl-4-substituted imidazole derivatives: new classes of dopamine receptor subtype specific ligands
JPH11513382A (ja) 1995-10-20 1999-11-16 ドクトル カルル トーマエ ゲゼルシャフト ミット ベシュレンクテル ハフツング 5員複素環化合物、これらの化合物を含む医薬品、それらの使用及びそれらの調製方法
EP0893446B1 (en) 1996-04-04 2006-10-04 Shionogi & Co., Ltd. Cephem compounds and drugs containing the compounds
JP4054992B2 (ja) 1996-04-25 2008-03-05 日産化学工業株式会社 エチレン誘導体および有害生物防除剤
AU736854B2 (en) 1996-04-25 2001-08-02 Nissan Chemical Industries Ltd. Ethylene derivatives and pesticides containing said derivatives
DE19624659A1 (de) 1996-06-20 1998-01-08 Klinge Co Chem Pharm Fab Neue Pyridylalken- und Pyridylalkinsäureamide
US5994398A (en) 1996-12-11 1999-11-30 Elan Pharmaceuticals, Inc. Arylsulfonamides as phospholipase A2 inhibitors
JP4416198B2 (ja) 1997-12-19 2010-02-17 武田薬品工業株式会社 アニリド誘導体、その製造法および用途
WO1999050264A1 (en) 1998-03-30 1999-10-07 Kyowa Hakko Kogyo Co., Ltd. Quinazoline derivatives
US6743585B2 (en) 1999-09-16 2004-06-01 Agilent Technologies, Inc. Methods for preparing conjugates
CO5271680A1 (es) 2000-02-21 2003-04-30 Smithkline Beecham Corp Compuestos
DE60115279T2 (de) 2000-09-29 2006-12-28 Topotarget Uk Ltd., Abingdon Carbaminsäurederivate enthaltend eine amidgruppe als hdac-inhibitoren
CN101851173A (zh) 2001-09-14 2010-10-06 梅特希尔基因公司 组蛋白脱乙酰化酶抑制剂
AU2003287965A1 (en) 2002-10-24 2004-05-13 Carex Sa Modulation of peroxisome proliferator activated receptors activity
DE10250743A1 (de) 2002-10-31 2004-05-19 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue Amid-Verbindungen mit MCH-antagonistischer Wirkung und diese Verbindungen enthaltende Arzneimittel
JP4145230B2 (ja) 2002-11-01 2008-09-03 武田薬品工業株式会社 神経障害の予防・治療剤
PE20040609A1 (es) 2002-11-01 2004-10-29 Takeda Pharmaceutical Compuestos heterociclicos aromaticos como promotores de un factor neurotrofico
EP1565452B1 (en) 2002-11-08 2012-04-04 Novartis International Pharmaceutical Ltd. 3-substituted-6-aryl pyridines as ligands of c5a receptors
EP1599447A1 (en) 2003-02-28 2005-11-30 Galderma Research & Development, S.N.C. Ligands that modulate lxr-type receptors
KR100966749B1 (ko) 2004-05-26 2010-06-30 에자이 알앤드디 매니지먼트 가부시키가이샤 신나미드 화합물
BRPI0515015A (pt) 2004-08-11 2008-07-01 Kyorin Seiyaku Kk derivado cìclico de ácido aminobenzóico; medicamento; agonista ppar(alpha); agonista duplo ppar(alpha), y; agonista duplo ppar(alpha), (delta); modulador ppar; agente lipìdeo; agente profilático ou terapêutico compreendendo pelo menos um dos derivados cìclicos de ácido aminobenzóico ou sal do mesmo farmacêuticamente aceitável
WO2006019020A1 (ja) 2004-08-16 2006-02-23 Sankyo Company, Limited 置換されたウレア化合物
JPWO2006088246A1 (ja) 2005-02-18 2008-07-10 武田薬品工業株式会社 Gpr34受容体機能調節剤
SI1954684T1 (sl) 2005-11-15 2014-07-31 Otsuka Pharmaceutical Co., Ltd. Oksazolna spojina in farmacevtski sestavek
JP2007210929A (ja) 2006-02-09 2007-08-23 Sankyo Co Ltd ウレア化合物を含有する医薬
HRP20120174T1 (hr) 2006-03-09 2012-03-31 Eisai R&D Management Co. Derivat policikličnog cinamida
KR101495611B1 (ko) 2006-04-07 2015-02-25 메틸진 인코포레이티드 히스톤 데아세틸라아제의 억제제
KR101507173B1 (ko) 2006-04-18 2015-03-30 닛뽕 케미파 가부시키가이샤 페록시좀 증식제 활성화 수용체 δ 의 활성화제
WO2007147336A1 (fr) 2006-06-13 2007-12-27 Shanghai Institue Of Materia Medica, Chinese Academy Of Sciences Composés non nucléosidiques hétérocycliques, leur préparation, compositions pharmaceutiques, et leur utilisation en tant qu'agents antiviraux
KR101410318B1 (ko) 2006-07-27 2014-06-27 (주)아모레퍼시픽 바닐로이드 수용체 길항제로서의 신규 화합물, 그의 이성질체, 또는 약제학적으로 허용가능한 그의 염, 및 이를함유하는 약제학적 조성물
ES2376668T3 (es) 2006-09-05 2012-03-15 Kyowa Hakko Kirin Co., Ltd. Derivado de imidazol.
EP1939180A1 (en) 2006-12-20 2008-07-02 sanofi-aventis Heteroarylacrylamides and their use as pharmaceuticals for the stimulation of the expression of endothelial NO synthase
EP1942104A1 (en) 2006-12-20 2008-07-09 sanofi-aventis Heteroarylcyclopropanecarboxamides and their use as pharmaceuticals
CN101711154A (zh) 2007-02-26 2010-05-19 科森生物科学公司 氨基甲酸酯化合物
EP2003118A1 (de) 2007-06-13 2008-12-17 Bayer Schering Pharma Aktiengesellschaft Zimtsäurederivate als Modulatoren des EP2-Rezeptors
US8106083B2 (en) 2008-08-08 2012-01-31 Synta Pharmaceuticals Corp. Triazole compounds that modulate HSP90 activity
WO2011006100A1 (en) 2009-07-09 2011-01-13 Crescendo Therapeutics, Llc Method of wound healing and scar modulation
WO2011069039A1 (en) 2009-12-04 2011-06-09 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Hydrazone and diacyl hydrazine compounds and methods of use
CN103002742B (zh) 2010-03-05 2016-07-13 卡尔约药物治疗公司 核转运调节剂及其应用
WO2012099807A1 (en) 2011-01-17 2012-07-26 Karyopharm Therapeutics, Inc. Olefin containing nuclear transport modulators and uses thereof
UA115532C2 (uk) 2011-07-29 2017-11-27 Каріофарм Терапеутікс, Інк. Модулятори нуклеарного транспорту, що містять гідразид, і їхнє застосування
WO2013019561A1 (en) 2011-07-29 2013-02-07 Karyopharm Therapeutics, Inc. Nuclear transport modulators and uses thereof
WO2013020024A2 (en) 2011-08-03 2013-02-07 Karyopharm Therapeutics, Inc. Maleimide compounds and methods of treatment
KR102163377B1 (ko) 2012-05-09 2020-10-08 바이오젠 엠에이 인코포레이티드 핵 수송 조절인자 및 이의 용도
EP2968278B8 (en) * 2013-03-15 2019-05-22 Karyopharm Therapeutics Inc. Methods of promoting wound healing using crm1 inhibitors
WO2014152263A1 (en) 2013-03-15 2014-09-25 Karyopharm Therapeutics Inc. Exo olefin-containing nuclear transport modulators and uses thereof
WO2014205393A1 (en) 2013-06-21 2014-12-24 Karyopharm Therapeutics Inc. Nuclear transport modulators and uses thereof
AU2014284168B2 (en) 2013-06-21 2018-10-25 Karyopharm Therapeutics Inc. Nuclear transport modulators and uses thereof
WO2015073908A1 (en) * 2013-11-15 2015-05-21 H. Lee Moffitt Cancer Center And Research Institute, Inc. Method for selecting cancer treatment regimen
EP3167288B1 (en) 2014-07-11 2021-10-20 Institut National de la Santé et de la Recherche Médicale (INSERM) Methods for diagnosing hematological cancers
WO2016015597A1 (en) * 2014-07-26 2016-02-04 Sunshine Lake Pharma Co., Ltd. Compounds as cdk small-molecule inhibitors and uses thereof
WO2016025904A1 (en) 2014-08-15 2016-02-18 Karyopharm Therapeutics Inc. Polymorphs of selinexor
EP3340996B1 (en) 2015-08-28 2022-02-23 The Trustees of Columbia University in the City of New York Systems and methods for matching oncology signatures
US10526295B2 (en) 2015-12-31 2020-01-07 Karyopharm Therapeutics Inc. Nuclear transport modulators and uses thereof
EP3397634A1 (en) 2015-12-31 2018-11-07 Karyopharm Therapeutics, Inc. Nuclear transport modulators and uses thereof
WO2017118940A1 (en) 2016-01-08 2017-07-13 Dr. Reddy's Laboratories Limited Solid forms of selinexor and process for their preparation
JP6765198B2 (ja) 2016-03-10 2020-10-07 パナソニック株式会社 潜熱蓄熱材及びそれを用いる蓄熱システム
US11602530B2 (en) 2016-11-28 2023-03-14 Biogen Ma Inc. CRM1 inhibitors for treating epilepsy
US10993943B2 (en) * 2017-01-05 2021-05-04 Watson Laboratories Inc. Crystalline forms of selinexor and process for their preparation
CN106831731B (zh) 2017-01-17 2019-11-08 广州市闻皓生物科技有限公司 一种Selinexor原料药的合成方法
KR20210143258A (ko) 2019-03-27 2021-11-26 카리오팜 쎄라퓨틱스, 인코포레이티드 셀리넥소를 위한 바이오마커
EP3808742A1 (en) 2019-10-16 2021-04-21 Sandoz AG Polymorph of selinexor
US11828455B2 (en) 2019-12-06 2023-11-28 Bae Systems Plc Light source
US20230391754A1 (en) 2020-10-21 2023-12-07 Karyopharm Therapeutics Inc. Crystalline form of selinexor

Also Published As

Publication number Publication date
US11746102B2 (en) 2023-09-05
US20180215733A1 (en) 2018-08-02
US11753401B2 (en) 2023-09-12
EP3180331B1 (en) 2022-06-08
US11078190B2 (en) 2021-08-03
JP2017527549A (ja) 2017-09-21
CN111481553A (zh) 2020-08-04
ZA201700880B (en) 2020-01-29
AU2021286266B2 (en) 2024-02-01
JP7218323B2 (ja) 2023-02-06
AU2015301484B2 (en) 2020-02-20
CA2957266A1 (en) 2016-02-18
EP3180331A1 (en) 2017-06-21
SG11201700789SA (en) 2017-02-27
ES2926377T3 (es) 2022-10-25
AU2021286266A1 (en) 2022-01-06
US10519139B2 (en) 2019-12-31
JP6777626B2 (ja) 2020-10-28
US20220135545A1 (en) 2022-05-05
MX2017002013A (es) 2017-05-12
US11807629B2 (en) 2023-11-07
EP4112615A1 (en) 2023-01-04
WO2016025904A1 (en) 2016-02-18
JP7558310B2 (ja) 2024-09-30
CN107072992B (zh) 2020-03-10
JP2020143144A (ja) 2020-09-10
US20230242517A1 (en) 2023-08-03
CN111481553B (zh) 2023-09-01
IL250328B (en) 2022-05-01
NZ728850A (en) 2024-03-22
MX2021014128A (es) 2022-01-04
US20200283419A1 (en) 2020-09-10
US12371420B2 (en) 2025-07-29
EA201790384A1 (ru) 2017-08-31
CN111484483A (zh) 2020-08-04
MX388170B (es) 2025-03-19
KR20170043561A (ko) 2017-04-21
MA40254A (fr) 2021-05-19
JP2023052622A (ja) 2023-04-11
UA123535C2 (uk) 2021-04-21
AU2020203246B2 (en) 2021-09-16
AU2024202835A1 (en) 2024-05-23
AU2020203246A1 (en) 2020-06-04
MA40254B1 (fr) 2022-09-30
US20230242516A1 (en) 2023-08-03
CN107072992A (zh) 2017-08-18
CO2017001884A2 (es) 2017-07-19
KR102608259B1 (ko) 2023-11-29
US20240208943A1 (en) 2024-06-27
CN111484483B (zh) 2023-05-26
AU2015301484A1 (en) 2017-03-02
SG10201808624VA (en) 2018-11-29
IL250328A0 (en) 2017-03-30

Similar Documents

Publication Publication Date Title
DK3180331T3 (da) Polymorfer af selinexor
DK3137169T3 (da) Hæmmere af lysin-specifik demethylase-1
DK3851537T5 (da) Behandling af hyperbilirubinæmi
DK3102576T3 (da) Dihydropyrrolopyridininhibitorer af ror-gamma
DK3192902T3 (da) Fremgangsmåde til fremstilling af graphenholdige viscosefibre
DK3201410T3 (da) Forbedringer af bygningsbeklædninger
DK3164380T3 (da) Hæmmere af lysinspecifik demethylase-1
DK3514109T3 (da) Hydropyrolyse af biomasseholdige råmaterialer
DK3117030T3 (da) Diagnosticering af sepsis
DK3558961T3 (da) Polymorfer
DK3558995T3 (da) Polymorfer
DK3132009T3 (da) Fremgangsmåde
DK3233813T3 (da) Fremgangsmåder til fremstilling af oxathiazin-lignende forbindelser
DK3220891T3 (da) Sublingual formulering af riluzol
DK3283210T3 (da) Fremgangsmåde
DK3418273T3 (da) Derivater af flavagliner
DK3204352T3 (da) Hæmmere af lysin-gingipain
DK3511000T3 (da) Krystallinsk form x2 af grapiprant
DK3137449T3 (da) Fremgangsmåder til fremstilling af substituerede cycloseriner
DK3297619T3 (da) Terapeutiske anvendelser af L-4-chlorkynurenin
DK3368044T3 (da) Behandling af hepatisk steatose-relateret oligo-ovulation
DK3201323T3 (da) Modificering af bakteriofag
IL254502A0 (en) Solid forms of menaquinols
DK2910535T3 (da) Sammensætning til anvendelse af ekspanderet perlit
DK3430004T3 (da) Faststofformer af nilotinibsalte