MA30786B1 - Procede d'optimisation de traitement de la leucemie philadelphie positive avec des inhibiteurs de tyrosine kinase abl. - Google Patents

Procede d'optimisation de traitement de la leucemie philadelphie positive avec des inhibiteurs de tyrosine kinase abl.

Info

Publication number
MA30786B1
MA30786B1 MA31775A MA31775A MA30786B1 MA 30786 B1 MA30786 B1 MA 30786B1 MA 31775 A MA31775 A MA 31775A MA 31775 A MA31775 A MA 31775A MA 30786 B1 MA30786 B1 MA 30786B1
Authority
MA
Morocco
Prior art keywords
leukemia
tyrosine kinase
abl tyrosine
cmin
bcr
Prior art date
Application number
MA31775A
Other languages
English (en)
Inventor
Francois-Xavier Mahon
Mathieu Molimard
Stephane Picard
Yanfeng Wang
Insa Gathmann
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=39092883&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA30786(B1) "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 MA30786B1 publication Critical patent/MA30786B1/fr

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
    • A61K31/495Heterocyclic 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
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/483Physical analysis of biological material
    • G01N33/487Physical analysis of biological material of liquid biological material
    • G01N33/49Blood
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2800/00Detection or diagnosis of diseases
    • G01N2800/52Predicting or monitoring the response to treatment, e.g. for selection of therapy based on assay results in personalised medicine; Prognosis

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Hematology (AREA)
  • Epidemiology (AREA)
  • Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • Immunology (AREA)
  • Ecology (AREA)
  • Pathology (AREA)
  • General Physics & Mathematics (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Urology & Nephrology (AREA)
  • Food Science & Technology (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (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)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

LA PRÉSENTE INVENTION CONCERNE UN PROCÉDÉ DE TRAITEMENT DE LA LEUCÉMIE PHILADELPHIE POSITIVE (PH+), TELLE QUE LA LEUCÉMIE LYMPHOBLASTE AIGUË POSITIVE DU CHROMOSOME DE PHILADELPHIE (PH+ ALL) OU LA LEUCÉMIE MYÉLOÏDE CHRONIQUE (LMC), CHEZ UN PATIENT HUMAIN COMPRENANT LES ÉTAPES SUIVANTES : (A) L'ADMINISTRATION D'UNE QUANTITÉ FIXE PRÉDÉTERMINÉE D'UN INHIBITEUR DE TYROSINE KINASE BCR-ABL, TEL QUE L'IMANITIB, OU UN SEL PHARMACEUTIQUEMENT ACCEPTABLE DE CELUI-CI À DES PATIENTS HUMAINS ATTEINTS DE LA LEUCÉMIE PH+, (B) LE PRÉLÈVEMENT D'AU MOINS UN ÉCHANTILLON SANGUIN DESDITS PATIENTS, (C) LA DÉTERMINATION DU NIVEAU DE LA CONCENTRATION PLASMIQUE MINIMALE(CMIN) DE L'INHIBITEUR DE TYROSINE KINASE OU D'UN MÉTABOLITE DE CELUI-CI AINSI QUE DES TAUX MMR, (D) L'ÉVALUATION D'UN POTENTIEL DE DISCRIMINATION DE CONCENTRATIONS DE DÉPRESSION PLASMIQUE POUR MMR ET L'IDENTIFICATION D'UN SEUIL CMIN POUR UNE SENSIBILITÉ ET UNE SPÉCIFICITÉ OPTIMALES ET (E)L'AJUSTEMENT DE LA DOSE DE L'INHIBITEUR DE TYROSINE KINASE BCR-ABL OU D'UN SEL PHARMACEUTIQUEMENT ACCEPTABLE DE CELUI-CI APPLIQUÉ À DES PATIENTS INDIVIDUELS PARMI LADITE POPULATION DE PATIENTS ET, ÉVENTUELLEMENT, DES PATIENTS FUTURS ATTEINTS DE LA LEUCÉMIE PH+ DE SORTE QU'UNE CMIN SOIT ATTEINT DANS CHAQUE PATIENT INDIVIDUEL ÉGAL OU INFÉRIEUR AU CMIN SEUIL OBTENU À L'ÉTAPE (D).
MA31775A 2006-09-22 2009-04-10 Procede d'optimisation de traitement de la leucemie philadelphie positive avec des inhibiteurs de tyrosine kinase abl. MA30786B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US82662206P 2006-09-22 2006-09-22
US82827806P 2006-10-05 2006-10-05

Publications (1)

Publication Number Publication Date
MA30786B1 true MA30786B1 (fr) 2009-10-01

Family

ID=39092883

Family Applications (1)

Application Number Title Priority Date Filing Date
MA31775A MA30786B1 (fr) 2006-09-22 2009-04-10 Procede d'optimisation de traitement de la leucemie philadelphie positive avec des inhibiteurs de tyrosine kinase abl.

Country Status (24)

Country Link
US (2) US20090281113A1 (fr)
EP (2) EP2251042A3 (fr)
JP (1) JP5735742B2 (fr)
KR (1) KR20090065512A (fr)
AT (1) ATE495761T1 (fr)
AU (1) AU2007299764B2 (fr)
BR (1) BRPI0717099A2 (fr)
CA (1) CA2662977A1 (fr)
CL (1) CL2007002725A1 (fr)
CY (1) CY1111356T1 (fr)
DE (1) DE602007012122D1 (fr)
DK (1) DK2068938T3 (fr)
HR (1) HRP20110250T1 (fr)
IL (1) IL197296A (fr)
MA (1) MA30786B1 (fr)
MX (1) MX2009003082A (fr)
NO (1) NO20091490L (fr)
NZ (1) NZ575113A (fr)
PL (1) PL2068938T3 (fr)
PT (1) PT2068938E (fr)
TN (1) TN2009000094A1 (fr)
TW (1) TWI398251B (fr)
WO (1) WO2008036792A2 (fr)
ZA (1) ZA200901220B (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL2237783T3 (pl) * 2008-01-23 2015-04-30 Novartis Ag Sposób optymalizacji leczenia chorób proliferacyjnych, w których pośredniczy receptor kinazy tyrozynowej kit, z użyciem imatynibu
US8697702B2 (en) 2008-12-01 2014-04-15 Novartis Ag Method of optimizing the treatment of Philadelphia-positive leukemia with imatinib mesylate
US20110046919A1 (en) 2009-03-02 2011-02-24 Juliesta Elaine Sylvester Method for accurate measurement of enzyme activities
FR2943418A1 (fr) * 2009-03-17 2010-09-24 Centre Nat Rech Scient Procedes de mesure de la quantite intracellulaire de molecules d'interet intrinsequement fluorescentes par cytometrie en flux et leurs applications
US20160289663A1 (en) * 2013-11-22 2016-10-06 National Center For Child Health And Development Novel chimeric gene atf7ip-pdgfrb of acute lymphoblastic leukemia
DK3319987T3 (da) * 2015-07-07 2021-06-21 Codexis Inc Nye p450-bm3-varianter med forbedret aktivitet
IT201900008808A1 (it) 2019-06-13 2020-12-13 Univ Ca Foscari Metodo per la determinazione della concentrazione di 4-[(4-metil-1-piperazinil)metil]-n-(4-metil-3-{[4-(3-piridinil)-2-pirimidinil]-ammino}fenil)benzammide(imatinib) in campioni di plasma
CN114994213A (zh) * 2022-06-28 2022-09-02 北京赛诺浦生物技术有限公司 一种测定人血浆中抗肿瘤药物酪氨酸激酶抑制血药浓度的试剂盒及测定方法

Family Cites Families (11)

* 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
CO4940418A1 (es) 1997-07-18 2000-07-24 Novartis Ag Modificacion de cristal de un derivado de n-fenil-2- pirimidinamina, procesos para su fabricacion y su uso
EP1169038B9 (fr) 1999-04-15 2013-07-10 Bristol-Myers Squibb Company Inhibiteurs cycliques de proteine tyrosine kinase
GB0202873D0 (en) 2002-02-07 2002-03-27 Novartis Ag Organic compounds
US20050164196A1 (en) * 2002-04-17 2005-07-28 Dressman Marlene M. Methods to predict patient responsiveness to tyrosine kinase inhibitors
GB0209265D0 (en) 2002-04-23 2002-06-05 Novartis Ag Organic compounds
GB0215676D0 (en) 2002-07-05 2002-08-14 Novartis Ag Organic compounds
GB0222514D0 (en) 2002-09-27 2002-11-06 Novartis Ag Organic compounds
AU2005254982B2 (en) 2004-06-10 2008-11-27 Irm Llc Compounds and compositions as protein kinase inhibitors
GB0421525D0 (en) 2004-09-28 2004-10-27 Novartis Ag Inhibitors of protein kineses
MY148074A (en) 2005-05-10 2013-02-28 Novartis Ag Pharmaceutical compositions comprising imatinib and a release retardant

Also Published As

Publication number Publication date
KR20090065512A (ko) 2009-06-22
TN2009000094A1 (en) 2010-08-19
WO2008036792A3 (fr) 2008-11-13
IL197296A (en) 2011-11-30
EP2068938A2 (fr) 2009-06-17
JP2010504353A (ja) 2010-02-12
CA2662977A1 (fr) 2008-03-27
HK1133194A1 (en) 2010-03-19
TW200822926A (en) 2008-06-01
EP2251042A3 (fr) 2012-05-02
WO2008036792A2 (fr) 2008-03-27
ATE495761T1 (de) 2011-02-15
CY1111356T1 (el) 2015-08-05
EP2068938B1 (fr) 2011-01-19
DK2068938T3 (da) 2011-04-04
NO20091490L (no) 2009-06-15
US20090281113A1 (en) 2009-11-12
PT2068938E (pt) 2011-03-23
JP5735742B2 (ja) 2015-06-17
BRPI0717099A2 (pt) 2013-10-15
US20170007605A1 (en) 2017-01-12
CL2007002725A1 (es) 2008-05-16
DE602007012122D1 (de) 2011-03-03
IL197296A0 (en) 2011-08-01
PL2068938T3 (pl) 2011-06-30
ZA200901220B (en) 2010-02-24
MX2009003082A (es) 2009-04-01
EP2251042A2 (fr) 2010-11-17
NZ575113A (en) 2012-03-30
AU2007299764A1 (en) 2008-03-27
TWI398251B (zh) 2013-06-11
HRP20110250T1 (hr) 2011-05-31
RU2009114856A (ru) 2010-10-27
AU2007299764B2 (en) 2011-10-13

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