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AR103711A2 - Procedimiento para modificar formación de cristal de fármaco, cristales modificados y composiciones que los contienen - Google Patents

Procedimiento para modificar formación de cristal de fármaco, cristales modificados y composiciones que los contienen

Info

Publication number
AR103711A2
AR103711A2 ARP160100409A ARP160100409A AR103711A2 AR 103711 A2 AR103711 A2 AR 103711A2 AR P160100409 A ARP160100409 A AR P160100409A AR P160100409 A ARP160100409 A AR P160100409A AR 103711 A2 AR103711 A2 AR 103711A2
Authority
AR
Argentina
Prior art keywords
drug substance
crystals
crystal habit
procedure
acicular
Prior art date
Application number
ARP160100409A
Other languages
English (en)
Original Assignee
Novartis Ag
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=9951448&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR103711(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of AR103711A2 publication Critical patent/AR103711A2/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/87Benzo [c] furans; Hydrogenated benzo [c] furans
    • C07D307/88Benzo [c] furans; Hydrogenated benzo [c] furans with one oxygen atom directly attached in position 1 or 3
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/28Dragees; Coated pills or tablets, e.g. with film or compression coating
    • A61K9/2806Coating materials
    • A61K9/2833Organic macromolecular compounds
    • A61K9/286Polysaccharides, e.g. gums; Cyclodextrin
    • A61K9/2866Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Immunology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Transplantation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Medicinal Preparation (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Furan Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Saccharide Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Se describe un procedimiento para modificar el hábito de cristal de sustancias de fármaco aciculares, cristales obtenidos a través de dicho procedimiento, y formas de cristal particulares o modificaciones de ácido micofenólico o micofenolato de sodio, así como composiciones farmacéuticas que comprenden los cristales, métodos y tratamiento y usos de los mismos. Reivindicación 1: Un procedimiento para modificar el hábito de cristal de una sustancia de fármaco acicular, caracterizada porque la sustancia de fármaco acicular es una sal de sodio de micofenolato, que comprende suspender dicha sustancia de fármaco cristalina en un sistema de solvente metanol / agua en una relación en el rango entre 98:2 y 90:10 y, y someter dicha suspensión a una oscilación de temperatura, donde el hábito de cristal es modificado y que la relación de aspecto media de los cristales procesados es menor que 10:1 y la densidad aparente es mayor que 200 kg/m³. Reivindicación 2: Un procedimiento para recristalizar una sustancia de fármaco acidular cristalina caracterizada porque la sustancia de fármaco acicular es una sal de sodio de micofenolato, que comprende suspender dicha sustancia de fármaco cristalina en un sistema de solvente metanol / agua en una relación en el rango entre 98:2 y 90:10 y, y someter dicha suspensión a una oscilación de temperatura, donde el hábito de cristal es modificado ya que la relación de aspecto media de los cristales procesados es menor que 10:1 y la densidad aparente es mayor que 200 kg/m³.
ARP160100409A 2003-01-20 2016-02-15 Procedimiento para modificar formación de cristal de fármaco, cristales modificados y composiciones que los contienen AR103711A2 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB0301259.8A GB0301259D0 (en) 2003-01-20 2003-01-20 Organic compounds

Publications (1)

Publication Number Publication Date
AR103711A2 true AR103711A2 (es) 2017-05-31

Family

ID=9951448

Family Applications (2)

Application Number Title Priority Date Filing Date
ARP040100142A AR043343A1 (es) 2003-01-20 2004-01-19 Procedimiento para modificar formacion de cristal de farmaco
ARP160100409A AR103711A2 (es) 2003-01-20 2016-02-15 Procedimiento para modificar formación de cristal de fármaco, cristales modificados y composiciones que los contienen

Family Applications Before (1)

Application Number Title Priority Date Filing Date
ARP040100142A AR043343A1 (es) 2003-01-20 2004-01-19 Procedimiento para modificar formacion de cristal de farmaco

Country Status (32)

Country Link
US (3) US20060122265A1 (es)
EP (2) EP2308471A1 (es)
JP (1) JP4549976B2 (es)
KR (5) KR100855149B1 (es)
CN (2) CN100595199C (es)
AR (2) AR043343A1 (es)
AT (1) ATE546132T1 (es)
AU (1) AU2004206731B2 (es)
BR (1) BRPI0406827A (es)
CA (2) CA2706900A1 (es)
CL (1) CL2004000073A1 (es)
CO (1) CO5580738A2 (es)
CY (1) CY1112772T1 (es)
DK (1) DK1592401T3 (es)
EC (1) ECSP055918A (es)
ES (1) ES2382035T3 (es)
GB (1) GB0301259D0 (es)
HK (1) HK1084874A1 (es)
IL (1) IL169484A (es)
MX (1) MXPA05007691A (es)
MY (1) MY148297A (es)
NO (1) NO20053846L (es)
NZ (1) NZ541073A (es)
PE (2) PE20110276A1 (es)
PL (2) PL376525A1 (es)
PT (1) PT1592401E (es)
RU (1) RU2388757C2 (es)
SG (1) SG155046A1 (es)
SI (1) SI1592401T1 (es)
TW (1) TWI325785B (es)
WO (1) WO2004064806A2 (es)
ZA (1) ZA200504442B (es)

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* Cited by examiner, † Cited by third party
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GB0124953D0 (en) 2001-10-17 2001-12-05 Novartis Ag Organic Compounds
GB0301259D0 (en) 2003-01-20 2003-02-19 Novartis Ag Organic compounds
AR045957A1 (es) * 2003-10-03 2005-11-16 Novartis Ag Composicion farmaceutica y combinacion
EP1740564A2 (en) 2004-04-26 2007-01-10 Teva Gyógyszergyár Zártköruen Muködo Részvenytarsaság Process for preparation of mycophenolic acid and ester derivatives thereof
CA2555461A1 (en) 2004-04-27 2005-11-10 Teva Gyogyszergyar Zartkoeruen Mukoedo Reszvenytarsasag Process for preparation of mycophenolate mofetil and other esters of mycophenolic acid
ATE461182T1 (de) * 2004-07-20 2010-04-15 Teva Gyogyszergyar Zartkoeruen Kristallines mycophenolat-natrium
GB0419355D0 (en) * 2004-08-31 2004-09-29 Novartis Ag Organic compounds
US20080176937A1 (en) * 2007-01-23 2008-07-24 Apotex Fermentation Inc. Novel crystalline mycophenolate sodium polymorph and processes to manufacture same
MX2011003731A (es) * 2008-10-09 2011-08-03 Abdi Ibrahim Ilac Sanayi Ve Ticaret Anonim Sirketi Uso de solventes organicos en la granulacion humeda de moxifloxacino.
CN101756958B (zh) * 2008-11-10 2011-07-20 鲁南制药集团股份有限公司 一种治疗关节炎的药物组合物及其制备方法
US20110009347A1 (en) 2009-07-08 2011-01-13 Yin Liang Combination therapy for the treatment of diabetes
ES2416459T3 (es) * 2009-07-10 2013-08-01 Janssen Pharmaceutica, N.V. Procedimiento de cristalización para 1-( -D-glucopiranosil)-4-metil-3-[5-(4-fluorofenil)-2-tienilmetil]benceno
WO2011046546A1 (en) * 2009-10-13 2011-04-21 Teva Pharmaceutical Industries Ltd. Delayed release compositions
CN108558740B (zh) 2010-01-27 2021-10-19 艾尼纳制药公司 S1p1受体调节剂及其盐的制备方法
CA2799204C (en) 2010-05-11 2018-11-06 Janssen Pharmaceutica Nv Pharmaceutical formulations comprising 1 - (beta-d-glucopyranosyl) - 2 -thienylmethylbenzene derivatives as inhibitors of sglt
CN103880800A (zh) * 2010-11-16 2014-06-25 北京京卫信康医药科技发展有限公司 麦考酚酸钠的新晶型及其制备方法
CN103880799A (zh) * 2010-11-16 2014-06-25 北京京卫信康医药科技发展有限公司 麦考酚酸钠的新晶型及其制备方法
ES2586846T3 (es) 2011-04-13 2016-10-19 Janssen Pharmaceutica, N.V. Proceso de preparación de compuestos útiles como inhibidores de SGLT2
TWI582078B (zh) * 2013-01-23 2017-05-11 北京貝美拓新藥研發有限公司 抑制脯氨酸羥化酶活性的化合物的晶型及其應用
MA42807A (fr) 2015-06-22 2018-07-25 Arena Pharm Inc Sel l-arginine cristallin d'acide (r)-2-(7-(4-cyclopentyl-3-(trifluorométhyl)benzyloxy)-1,2,3,4-tétrahydrocyclo-penta[b]indol-3-yl)acétique (composé 1) pour une utilisation dans des troubles associés au récepteur de s1p1
US20170071970A1 (en) 2015-09-15 2017-03-16 Janssen Pharmaceutica Nv Co-therapy comprising canagliflozin and phentermine for the treatment of obesity and obesity related disorders
US10323025B2 (en) * 2015-12-21 2019-06-18 Janssen Pharmaceutica Nv Crystallization procedure for obtaining canagliflozin hemihydrate crystals
US11478448B2 (en) 2017-02-16 2022-10-25 Arena Pharmaceuticals, Inc. Compounds and methods for treatment of inflammatory bowel disease with extra-intestinal manifestations
MA47504A (fr) 2017-02-16 2019-12-25 Arena Pharm Inc Composés et méthodes de traitement de l'angiocholite biliaire primitive
CN108727317A (zh) * 2017-04-25 2018-11-02 鲁南制药集团股份有限公司 一种麦考酚酸的晶型物
CN108727318A (zh) * 2017-04-25 2018-11-02 鲁南制药集团股份有限公司 麦考酚酸的晶型物
CN110922371B (zh) * 2019-12-27 2020-08-11 广东蓝宝制药有限公司 一种m2晶型麦考酚钠的制备方法
WO2023234158A1 (ja) * 2022-05-31 2023-12-07 本州化学工業株式会社 4,4'-ビス(1,1-ビス(4-ヒドロキシ-3-メチルフェニル)エチル)ビフェニルの結晶及び、その製造方法

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Also Published As

Publication number Publication date
KR101129105B1 (ko) 2012-04-12
WO2004064806A2 (en) 2004-08-05
MXPA05007691A (es) 2005-09-30
SG155046A1 (en) 2009-09-30
US8124795B2 (en) 2012-02-28
RU2388757C2 (ru) 2010-05-10
CA2706900A1 (en) 2004-08-05
PT1592401E (pt) 2012-05-10
ES2382035T3 (es) 2012-06-04
CL2004000073A1 (es) 2005-01-14
DK1592401T3 (da) 2012-05-21
EP1592401A2 (en) 2005-11-09
PE20040826A1 (es) 2004-12-23
JP2006515016A (ja) 2006-05-18
KR100855149B1 (ko) 2008-08-28
SI1592401T1 (sl) 2012-05-31
EP1592401B1 (en) 2012-02-22
CN100595199C (zh) 2010-03-24
ECSP055918A (es) 2005-11-22
PL376525A1 (pl) 2006-01-09
CA2509796C (en) 2010-09-14
KR20050096940A (ko) 2005-10-06
EP2308471A1 (en) 2011-04-13
US20060122265A1 (en) 2006-06-08
KR20090115821A (ko) 2009-11-06
NZ541073A (en) 2008-12-24
CO5580738A2 (es) 2005-11-30
ATE546132T1 (de) 2012-03-15
RU2005126328A (ru) 2006-07-27
KR20090115898A (ko) 2009-11-09
IL169484A (en) 2016-03-31
CN1738605A (zh) 2006-02-22
CN101333201A (zh) 2008-12-31
AU2004206731B2 (en) 2008-03-20
GB0301259D0 (en) 2003-02-19
ZA200504442B (en) 2006-02-22
CY1112772T1 (el) 2016-02-10
BRPI0406827A (pt) 2005-12-27
AR043343A1 (es) 2005-07-27
MY148297A (en) 2013-03-29
WO2004064806A3 (en) 2004-10-28
IL169484A0 (en) 2007-07-04
CA2509796A1 (en) 2004-08-05
TW200505505A (en) 2005-02-16
JP4549976B2 (ja) 2010-09-22
US20110288313A1 (en) 2011-11-24
AU2004206731A1 (en) 2004-08-05
TWI325785B (en) 2010-06-11
HK1084874A1 (en) 2006-08-11
AU2004206731A8 (en) 2004-08-05
PL213192B1 (pl) 2013-01-31
NO20053846L (no) 2005-08-16
US20090209639A1 (en) 2009-08-20
PE20110276A1 (es) 2011-05-27
PL393385A1 (pl) 2011-03-14
KR20070087181A (ko) 2007-08-27
KR20100120321A (ko) 2010-11-15
US8008511B2 (en) 2011-08-30

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