JP2023506118A - 皮膚エリテマトーデス及び扁平苔癬(lp)の治療のためのjak1阻害剤の使用 - Google Patents

皮膚エリテマトーデス及び扁平苔癬(lp)の治療のためのjak1阻害剤の使用 Download PDF

Info

Publication number
JP2023506118A
JP2023506118A JP2022523053A JP2022523053A JP2023506118A JP 2023506118 A JP2023506118 A JP 2023506118A JP 2022523053 A JP2022523053 A JP 2022523053A JP 2022523053 A JP2022523053 A JP 2022523053A JP 2023506118 A JP2023506118 A JP 2023506118A
Authority
JP
Japan
Prior art keywords
pyrrolo
pyrimidin
jak1
pyrazol
acetonitrile
Prior art date
Legal status (The legal status 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 status listed.)
Pending
Application number
JP2022523053A
Other languages
English (en)
Japanese (ja)
Inventor
スミス,ポール
ヴェンツェル,イェルク
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Incyte Corp
Original Assignee
Incyte Corp
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 Incyte Corp filed Critical Incyte Corp
Publication of JP2023506118A publication Critical patent/JP2023506118A/ja
Pending legal-status Critical Current

Links

Images

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
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • 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
    • A61K31/4151,2-Diazoles
    • A61K31/41551,2-Diazoles non condensed and containing further heterocyclic rings
    • 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
    • A61K31/437Heterocyclic 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 the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
JP2022523053A 2019-10-16 2019-10-16 皮膚エリテマトーデス及び扁平苔癬(lp)の治療のためのjak1阻害剤の使用 Pending JP2023506118A (ja)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US2019/056533 WO2021076124A1 (fr) 2019-10-16 2019-10-16 Utilisation d'inhibiteurs de jak1 pour le traitement du lupus érythémateux cutané et du lichen plan (l.p.)

Publications (1)

Publication Number Publication Date
JP2023506118A true JP2023506118A (ja) 2023-02-15

Family

ID=68470631

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2022523053A Pending JP2023506118A (ja) 2019-10-16 2019-10-16 皮膚エリテマトーデス及び扁平苔癬(lp)の治療のためのjak1阻害剤の使用

Country Status (2)

Country Link
JP (1) JP2023506118A (fr)
WO (1) WO2021076124A1 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4221711A1 (fr) * 2020-10-02 2023-08-09 Incyte Corporation Ruxolitinib topique pour le traitement de lichen plan
CA3219092A1 (fr) * 2021-05-03 2022-11-10 Incyte Corporation Inhibiteurs de la voie jak1 pour le traitement du prurigo nodulaire

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013522214A (ja) * 2010-03-10 2013-06-13 インサイト・コーポレイション Jak1阻害剤としてのピペリジン−4−イルアゼチジン誘導体
JP2015535288A (ja) * 2012-11-01 2015-12-10 インサイト・コーポレイションIncyte Corporation Jak阻害薬としての三環式縮合チオフェン誘導体
JP2016519147A (ja) * 2013-05-17 2016-06-30 インサイト・コーポレイションIncyte Corporation Jak阻害剤としてのビピラゾール誘導体
JP2019506422A (ja) * 2016-02-16 2019-03-07 キム,ブライアン Jak阻害剤およびこれらの利用
WO2019191679A1 (fr) * 2018-03-30 2019-10-03 Incyte Corporation Biomarqueurs pour maladie cutanée inflammatoire

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5521184A (en) 1992-04-03 1996-05-28 Ciba-Geigy Corporation Pyrimidine derivatives and processes for the preparation thereof
EP1107964B8 (fr) 1998-08-11 2010-04-07 Novartis AG Derives d'isoquinoline possedant une activite d'inhibition de l'angiogenese
US6133031A (en) 1999-08-19 2000-10-17 Isis Pharmaceuticals Inc. Antisense inhibition of focal adhesion kinase expression
GB9905075D0 (en) 1999-03-06 1999-04-28 Zeneca Ltd Chemical compounds
GB0004890D0 (en) 2000-03-01 2000-04-19 Astrazeneca Uk Ltd Chemical compounds
CZ303572B6 (cs) 2000-06-28 2012-12-12 Smithkline Beecham P. L. C. Jemne rozmelnený prostredek a zpusob jeho prípravy
NZ531378A (en) 2001-09-19 2006-11-30 Aventis Pharma S Indolizines as kinase protein inhibitors suitable for treating solid tumours
PT1441737E (pt) 2001-10-30 2006-12-29 Dana Farber Cancer Inst Inc Derivados de estrutura como inibidores da actividade do receptor de tirosina cinase flt3
AR037647A1 (es) 2002-05-29 2004-12-01 Novartis Ag Derivados de diarilurea utiles para el tratamiento de enfermedades dependientes de la cinasa de proteina
GB0215676D0 (en) 2002-07-05 2002-08-14 Novartis Ag Organic compounds
TWI335913B (en) 2002-11-15 2011-01-11 Vertex Pharma Diaminotriazoles useful as inhibitors of protein kinases
UA80767C2 (en) 2002-12-20 2007-10-25 Pfizer Prod Inc Pyrimidine derivatives for the treatment of abnormal cell growth
GB0305929D0 (en) 2003-03-14 2003-04-23 Novartis Ag Organic compounds
PE20050952A1 (es) 2003-09-24 2005-12-19 Novartis Ag Derivados de isoquinolina como inhibidores de b-raf
KR20070085433A (ko) 2004-11-24 2007-08-27 노파르티스 아게 Jak 저해제들과 bcr-abl, flt-3, fak 또는raf 키나제 저해제들 중 하나 이상의 조합물
TWI468162B (zh) 2005-12-13 2015-01-11 英塞特公司 作為傑納斯激酶(JANUS KINASE)抑制劑之經雜芳基取代之吡咯并〔2,3-b〕吡啶及吡咯并〔2,3-b〕嘧啶
SG10201509887UA (en) 2007-06-13 2016-01-28 Incyte Corp Salts of the janus kinase inhibitor (r)-3-(4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl)-3-cyclopentylpropanenitrile
EA025520B1 (ru) 2009-05-22 2017-01-30 Инсайт Холдингс Корпорейшн N-(ГЕТЕРО)АРИЛПИРРОЛИДИНОВЫЕ ПРОИЗВОДНЫЕ ПИРАЗОЛ-4-ИЛ-ПИРРОЛО[2,3-d]ПИРИМИДИНОВ И ПИРРОЛ-3-ИЛ-ПИРРОЛО[2,3-d]ПИРИМИДИНОВ В КАЧЕСТВЕ ИНГИБИТОРОВ ЯНУС-КИНАЗЫ
WO2011028685A1 (fr) 2009-09-01 2011-03-10 Incyte Corporation Dérivés hétérocycliques de pyrazol-4-yl-pyrrolo[2,3-d] pyrimidines en tant qu'inhibiteurs de janus kinase
US9034884B2 (en) 2010-11-19 2015-05-19 Incyte Corporation Heterocyclic-substituted pyrrolopyridines and pyrrolopyrimidines as JAK inhibitors
WO2012068450A1 (fr) 2010-11-19 2012-05-24 Incyte Corporation Dérivés pyrrolopyridine et pyrrolopyrimidine à substitution cyclobutyle utilisés comme inhibiteurs des jak
CA2839767A1 (fr) 2011-06-20 2012-12-27 Incyte Corporation Derives d'azetidinyl-phenyl-, de pyridyl- ou de pyrazinyl-carboxamide en tant qu'inhibiteurs des jak
TW201313721A (zh) 2011-08-18 2013-04-01 Incyte Corp 作為jak抑制劑之環己基氮雜環丁烷衍生物
UA111854C2 (uk) 2011-09-07 2016-06-24 Інсайт Холдінгс Корпорейшн Способи і проміжні сполуки для отримання інгібіторів jak
US9193733B2 (en) 2012-05-18 2015-11-24 Incyte Holdings Corporation Piperidinylcyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as JAK inhibitors
US20150197525A1 (en) 2012-06-15 2015-07-16 Concert Pharmaceuticals, Inc. Deuterated derivatives of ruxolitinib
AU2013302519B2 (en) 2012-08-17 2017-11-02 Concert Pharmaceuticals, Inc. Deuterated baricitinib
CN105189509B (zh) 2013-03-06 2017-12-19 因赛特公司 用于制备jak抑制剂的方法及中间体
MA39987A (fr) 2014-04-30 2017-03-08 Incyte Corp Procédés de préparation d'un inhibiteur de jak1 et nouvelles formes associées
EP3538103A1 (fr) * 2016-11-10 2019-09-18 Galapagos NV Composés et compositions pharmaceutiques associées pour le traitement de maladies inflammatoires

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013522214A (ja) * 2010-03-10 2013-06-13 インサイト・コーポレイション Jak1阻害剤としてのピペリジン−4−イルアゼチジン誘導体
JP2015535288A (ja) * 2012-11-01 2015-12-10 インサイト・コーポレイションIncyte Corporation Jak阻害薬としての三環式縮合チオフェン誘導体
JP2016519147A (ja) * 2013-05-17 2016-06-30 インサイト・コーポレイションIncyte Corporation Jak阻害剤としてのビピラゾール誘導体
JP2019506422A (ja) * 2016-02-16 2019-03-07 キム,ブライアン Jak阻害剤およびこれらの利用
WO2019191679A1 (fr) * 2018-03-30 2019-10-03 Incyte Corporation Biomarqueurs pour maladie cutanée inflammatoire

Non-Patent Citations (8)

* Cited by examiner, † Cited by third party
Title
"History of Changes for Study: NCT03134222 Safety and Efficacy of Filgotinib and Lanraplenib in Fema", CLINICALTRIALS.GOV ARCHIVE, JPN6023040052, 20 February 2019 (2019-02-20), ISSN: 0005167246 *
"History of Changes for Study: NCT03288324 Open label Study of Tofacitinib for Moderate to Severe Sk", CLINICALTRIALS.GOV ARCHIVE, JPN6023040050, 22 July 2019 (2019-07-22), ISSN: 0005167245 *
ANNALS OF THE RHEUMATIC DISEASES, vol. Vol.78, Issue Supplement 2, JPN6023040054, 2019, pages 1487 - 0042, ISSN: 0005167240 *
FRONTIERS IN IMMUNOLOGY, vol. Vol.10, Article number 1862, JPN6023040048, 2019, pages 1 - 21, ISSN: 0005167247 *
JOURNAL OF INVESTIGATIVE DERMATOLOGY, vol. 128, no. 10, JPN6023040047, 2008, pages 2392 - 2402, ISSN: 0005167243 *
JOURNAL OF INVESTIGATIVE DERMATOLOGY, vol. 129, no. 2, JPN6023040045, 2009, pages 315 - 319, ISSN: 0005167242 *
JOURNAL OF INVESTIGATIVE DERMATOLOGY, vol. 135, no. 7, JPN6023040049, 2015, pages 1912 - 1915, ISSN: 0005167244 *
日本臨床免疫学会会誌, vol. 38, no. 1, JPN6023040043, 2015, pages 1 - 7, ISSN: 0005167241 *

Also Published As

Publication number Publication date
WO2021076124A1 (fr) 2021-04-22

Similar Documents

Publication Publication Date Title
JP7206314B2 (ja) Jak及びpi3k阻害剤併用によるb細胞悪性腫瘍の処置
US20220241286A1 (en) Treatment of hidradenitis suppurativa using jak inhibitors
US11833152B2 (en) JAK1 pathway inhibitors for the treatment of cytokine-related disorders
US20150342952A1 (en) TREATMENT OF CHRONIC NEUTROPHILIC LEUKEMIA (CNL) AND ATYPICAL CHRONIC MYELOID LEUKEMIA (aCML) BY INHIBITORS OF JAK1
EP2714686A1 (fr) Dérivés de pyridin-2(1h)-one utiles en tant que médicaments pour le traitement de troubles myéloprolifératifs, du rejet de greffe, de maladies à médiation immunitaire et inflammatoires
WO2013017461A1 (fr) Dérivés de pyridin-2(1h)-one en tant qu'inhibiteurs de jak
US20230257410A1 (en) Phenothiazine derivatives and uses thereof
JP2023506118A (ja) 皮膚エリテマトーデス及び扁平苔癬(lp)の治療のためのjak1阻害剤の使用
US20210113566A1 (en) Use of jak1 inhibitors for the treatment of cutaneous lupus erythematosus and lichen planus (lp)
JP7406264B2 (ja) 皮膚障害の処置のためのシアノアリール-アニリン化合物
JP6279465B2 (ja) 治療計画
TWI835786B (zh) 使用jak抑制劑治療化膿性汗腺炎
US20240058343A1 (en) Treatment of urticaria using jak inhibitors
KR20230157307A (ko) Jak 경로 억제제 및 rock 억제제를 포함하는 병용 요법
EA042956B1 (ru) Ингибиторы пути jak1, предназначенные для лечения связанных с цитокинами нарушений
CN117120055A (zh) 包含jak通路抑制剂和rock抑制剂的组合疗法
ZA200700129B (en) Combination of a selective noradrenaline reuptake inhibitor and a PDEV inhibitor

Legal Events

Date Code Title Description
A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20221014

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20221014

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20230925

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20231003

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20231226

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20240229

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20240403