PE20151157A1 - Formas de dosificacion de ruxolitinib de liberacion sostenida - Google Patents

Formas de dosificacion de ruxolitinib de liberacion sostenida

Info

Publication number
PE20151157A1
PE20151157A1 PE2015000624A PE2015000624A PE20151157A1 PE 20151157 A1 PE20151157 A1 PE 20151157A1 PE 2015000624 A PE2015000624 A PE 2015000624A PE 2015000624 A PE2015000624 A PE 2015000624A PE 20151157 A1 PE20151157 A1 PE 20151157A1
Authority
PE
Peru
Prior art keywords
ruxolitinib
dosage forms
sustained release
useful
treatment
Prior art date
Application number
PE2015000624A
Other languages
English (en)
Spanish (es)
Inventor
Yong Ni
Krishnaswamy Yeleswaram
Susan Erickson-Viitanen
William V Williams
Bhavnish Parikh
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=49681181&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20151157(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Incyte Corp filed Critical Incyte Corp
Publication of PE20151157A1 publication Critical patent/PE20151157A1/es

Links

Classifications

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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2022—Organic macromolecular compounds
    • A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • A—HUMAN NECESSITIES
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Diabetes (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Virology (AREA)
  • Rheumatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Neurology (AREA)
  • Epidemiology (AREA)
  • Endocrinology (AREA)
  • Communicable Diseases (AREA)
  • Obesity (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Molecular Biology (AREA)
  • Dermatology (AREA)
  • Urology & Nephrology (AREA)
  • Nutrition Science (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pulmonology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Biotechnology (AREA)
  • Vascular Medicine (AREA)
PE2015000624A 2012-11-15 2013-11-14 Formas de dosificacion de ruxolitinib de liberacion sostenida PE20151157A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261726893P 2012-11-15 2012-11-15
US201361769408P 2013-02-26 2013-02-26

Publications (1)

Publication Number Publication Date
PE20151157A1 true PE20151157A1 (es) 2015-08-19

Family

ID=49681181

Family Applications (2)

Application Number Title Priority Date Filing Date
PE2019001988A PE20200175A1 (es) 2012-11-15 2013-11-14 Formas de dosificacion de ruxolitinib de liberacion sostenida
PE2015000624A PE20151157A1 (es) 2012-11-15 2013-11-14 Formas de dosificacion de ruxolitinib de liberacion sostenida

Family Applications Before (1)

Application Number Title Priority Date Filing Date
PE2019001988A PE20200175A1 (es) 2012-11-15 2013-11-14 Formas de dosificacion de ruxolitinib de liberacion sostenida

Country Status (34)

Country Link
US (9) US10166191B2 (enExample)
EP (2) EP3949953A1 (enExample)
JP (4) JP2015537030A (enExample)
KR (3) KR102242077B1 (enExample)
CN (3) CN113384546A (enExample)
AR (1) AR093490A1 (enExample)
AU (4) AU2013344780B2 (enExample)
BR (1) BR112015010663B1 (enExample)
CA (2) CA2890755C (enExample)
CL (1) CL2015001286A1 (enExample)
CR (2) CR20190073A (enExample)
CY (1) CY1124446T1 (enExample)
DK (1) DK2919766T3 (enExample)
EA (1) EA201590930A1 (enExample)
ES (1) ES2880814T3 (enExample)
HR (1) HRP20211158T1 (enExample)
HU (1) HUE055894T2 (enExample)
IL (4) IL317061A (enExample)
LT (1) LT2919766T (enExample)
MX (3) MX380147B (enExample)
MY (1) MY191357A (enExample)
NZ (2) NZ708157A (enExample)
PE (2) PE20200175A1 (enExample)
PH (2) PH12020551186B1 (enExample)
PL (1) PL2919766T3 (enExample)
PT (1) PT2919766T (enExample)
RS (1) RS62329B1 (enExample)
SG (3) SG10202111768XA (enExample)
SI (1) SI2919766T1 (enExample)
SM (1) SMT202100436T1 (enExample)
TW (4) TW202228704A (enExample)
UA (1) UA120834C2 (enExample)
WO (1) WO2014078486A1 (enExample)
ZA (1) ZA202202711B (enExample)

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EP2432555B1 (en) 2009-05-22 2014-04-30 Incyte Corporation N-(hetero)aryl-pyrrolidine derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines and pyrrol-3-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors
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WO2015184305A1 (en) 2014-05-30 2015-12-03 Incyte Corporation TREATMENT OF CHRONIC NEUTROPHILIC LEUKEMIA (CNL) AND ATYPICAL CHRONIC MYELOID LEUKEMIA (aCML) BY INHIBITORS OF JAK1
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