US5506219A
(en)
*
|
1988-08-29 |
1996-04-09 |
E. R. Squibb & Sons, Inc. |
Pyridine anchors for HMG-CoA reductase inhibitors
|
DE4243279A1
(de)
*
|
1992-12-21 |
1994-06-23 |
Bayer Ag |
Substituierte Triole
|
DE4244029A1
(de)
*
|
1992-12-24 |
1994-06-30 |
Bayer Ag |
Neue substituierte Pyridine
|
DE4309553A1
(de)
*
|
1993-03-24 |
1994-09-29 |
Bayer Ag |
Verfahren zur Herstellung von 3R,5S-(+)-Natrium-erythro-(E)-7-(4-(4-flurophenyl)-2,6-diisopropyl-5-methoxymethyl-pyrid-3-yl)-3,5-dihydroxy-hept-6-enoat
|
US5677455A
(en)
*
|
1994-09-06 |
1997-10-14 |
Ube Industries, Ltd. |
Preparation of 3-oxy-5-oxo-6-heptenoic acid derivatives
|
PL329614A1
(en)
|
1996-04-16 |
1999-03-29 |
Bayer Ag |
D-mannitoll and method of obtaining same
|
DE19627420A1
(de)
*
|
1996-07-08 |
1998-01-15 |
Bayer Ag |
6-(Hydroxymethyl-ethyl)pyridine
|
DE19714343A1
(de)
|
1997-04-08 |
1998-10-15 |
Bayer Ag |
Chromatographische Enantiomerentrennung von Lactonen
|
US8679534B2
(en)
*
|
1997-12-12 |
2014-03-25 |
Andrx Labs, Llc |
HMG-CoA reductase inhibitor extended release formulation
|
US20030078211A1
(en)
*
|
1998-06-24 |
2003-04-24 |
Merck & Co., Inc. |
Compositions and methods for inhibiting bone resorption
|
WO1999067809A1
(fr)
|
1998-06-24 |
1999-12-29 |
Merck & Co., Inc. |
Compositions et procedes inhibant la resorption osseuse
|
DE19858789A1
(de)
|
1998-12-18 |
2000-06-21 |
Bayer Ag |
Kombination von Cerivastatin und Fibraten
|
US6569461B1
(en)
|
1999-03-08 |
2003-05-27 |
Merck & Co., Inc. |
Dihydroxy open-acid and salts of HMG-CoA reductase inhibitors
|
GB0003305D0
(en)
*
|
2000-02-15 |
2000-04-05 |
Zeneca Ltd |
Pyrimidine derivatives
|
US6395767B2
(en)
|
2000-03-10 |
2002-05-28 |
Bristol-Myers Squibb Company |
Cyclopropyl-fused pyrrolidine-based inhibitors of dipeptidyl peptidase IV and method
|
AU2001257022B2
(en)
*
|
2000-04-13 |
2005-02-03 |
Mayo Foundation For Medical Education And Research |
Abeta 42 lowering agents
|
US6812345B2
(en)
|
2000-06-15 |
2004-11-02 |
Bristol-Myers Squibb Company |
HMG-CoA reductase inhibitors and method
|
US20020013334A1
(en)
*
|
2000-06-15 |
2002-01-31 |
Robl Jeffrey A. |
HMG-CoA reductase inhibitors and method
|
US6627636B2
(en)
|
2000-06-15 |
2003-09-30 |
Bristol-Myers Squibb Company |
HMG-CoA reductase inhibitors and method
|
US6620821B2
(en)
|
2000-06-15 |
2003-09-16 |
Bristol-Myers Squibb Company |
HMG-CoA reductase inhibitors and method
|
JO2654B1
(en)
*
|
2000-09-04 |
2012-06-17 |
شركة جانسين فارماسوتيكا ان. في |
Multiple aryl caroxa amides are useful as lipid - lowering agents
|
US20030162829A1
(en)
*
|
2000-10-06 |
2003-08-28 |
George Kindness |
Combination of treatment of cancer utilizing a COX-2 inhibitor and a 3-hydroxy-3-methylglutaryl-coenzyme-a (HMG-CoA) reductase inhibitor
|
US6534540B2
(en)
|
2000-10-06 |
2003-03-18 |
George Kindness |
Combination and method of treatment of cancer utilizing a COX-2 inhibitor and a 3-hydroxy-3-methylglutaryl-coenzyme-a (HMG-CoA) reductase inhibitor
|
RU2003113328A
(ru)
*
|
2000-10-12 |
2004-09-10 |
Ниссан Кемикал Индастриз, Лтд (Jp) |
Профилактическое и терапевтическое средство для лечения осложнений, связанных с диабетом
|
US6777552B2
(en)
*
|
2001-08-16 |
2004-08-17 |
Teva Pharmaceutical Industries, Ltd. |
Processes for preparing calcium salt forms of statins
|
JO2409B1
(en)
*
|
2000-11-21 |
2007-06-17 |
شركة جانسين فارماسوتيكا ان. في |
Second-phenyl carboxy amides are useful as lipid-lowering agents
|
AU2002219175A1
(en)
*
|
2000-12-21 |
2002-07-01 |
Ciba Speciality Chemicals Holding Inc. |
Crystalline forms of cerivastatin sodium
|
JO2390B1
(en)
|
2001-04-06 |
2007-06-17 |
شركة جانسين فارماسوتيكا ان. في |
Diphenylcarboxamides act as lipid-lowering agents
|
WO2002083066A2
(fr)
|
2001-04-11 |
2002-10-24 |
Bristol-Myers Squibb Company |
Complexes acides amines de glugocides c-aryle pour le traitement du diabete et procede correspondant
|
AU2002257147B9
(en)
*
|
2001-04-18 |
2005-08-18 |
Genzyme Corporation |
Methods of treating syndrome X with aliphatic polyamines
|
US20040092565A1
(en)
*
|
2001-07-25 |
2004-05-13 |
George Kindness |
Composition and method of sustaining chemotherapeutic effect while reducing dose of chemotherapeutic agent using cox-2 inhibitor and statin
|
US7122143B2
(en)
|
2001-09-28 |
2006-10-17 |
Mcneil-Ppc, Inc. |
Methods for manufacturing dosage forms
|
US7238671B2
(en)
*
|
2001-10-18 |
2007-07-03 |
Bristol-Myers Squibb Company |
Human glucagon-like-peptide-1 mimics and their use in the treatment of diabetes and related conditions
|
RU2353625C2
(ru)
*
|
2001-10-18 |
2009-04-27 |
Бристол-Маерс Сквибб Компани |
Миметики человеческого глюканоподобного пептида-1 и их применение в лечении диабета и родственных состояний
|
US6806381B2
(en)
*
|
2001-11-02 |
2004-10-19 |
Bristol-Myers Squibb Company |
Process for the preparation of aniline-derived thyroid receptor ligands
|
EP1443919A4
(fr)
*
|
2001-11-16 |
2006-03-22 |
Bristol Myers Squibb Co |
Inhibiteurs doubles de la proteine de liaison des acides gras des adipocytes et de la proteine de liaison des acides gras des keratinocytes
|
US6831102B2
(en)
*
|
2001-12-07 |
2004-12-14 |
Bristol-Myers Squibb Company |
Phenyl naphthol ligands for thyroid hormone receptor
|
WO2003060078A2
(fr)
*
|
2001-12-21 |
2003-07-24 |
X-Ceptor Therapeutics, Inc. |
Modulateurs heterocycliques de recepteurs nucleaires
|
EP1465869B1
(fr)
*
|
2001-12-21 |
2013-05-15 |
Exelixis Patent Company LLC |
Modulateurs de lxr
|
US7482366B2
(en)
|
2001-12-21 |
2009-01-27 |
X-Ceptor Therapeutics, Inc. |
Modulators of LXR
|
JP4625637B2
(ja)
|
2002-02-22 |
2011-02-02 |
シャイア エルエルシー |
活性物質送達系及び活性物質を保護し投与する方法
|
US20050113577A1
(en)
*
|
2002-04-16 |
2005-05-26 |
Karki Shyam B. |
Solid forms of slats with tyrosine kinase activity
|
DE10216967A1
(de)
*
|
2002-04-16 |
2003-11-13 |
Bayer Ag |
Verfahren zur Herstellung spezieller aromatischer Aldehyde
|
AU2003225305A1
(en)
|
2002-05-08 |
2003-11-11 |
Bristol-Myers Squibb Company |
Pyridine-based thyroid receptor ligands
|
WO2003096548A2
(fr)
*
|
2002-05-14 |
2003-11-20 |
Siemens Aktiengesellschaft |
Procede pour generer un signal d'emission
|
US7057046B2
(en)
*
|
2002-05-20 |
2006-06-06 |
Bristol-Myers Squibb Company |
Lactam glycogen phosphorylase inhibitors and method of use
|
CA2488498A1
(fr)
|
2002-06-10 |
2003-12-18 |
Elan Pharma International Limited |
Formulation de polycosanol nanoparticulaires et nouvelles combinaisons de polycosanol
|
MXPA05000913A
(es)
*
|
2002-07-23 |
2005-03-23 |
Nutrinova Gmbh |
Agente reductor de colesterol hecho a partir de fibra dietetica y sustancias reductoras de colesterol.
|
UA79300C2
(en)
|
2002-08-12 |
2007-06-11 |
Janssen Pharmaceutica Nv |
N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein b secretion
|
US20080293750A1
(en)
*
|
2002-10-17 |
2008-11-27 |
Anna Helgadottir |
Susceptibility Gene for Myocardial Infarction, Stroke, Paod and Methods of Treatment
|
ATE469645T1
(de)
*
|
2002-10-23 |
2010-06-15 |
Bristol Myers Squibb Co |
Auf glycinnitril basierende hemmer der dipeptidylpeptidase iv
|
US7098235B2
(en)
|
2002-11-14 |
2006-08-29 |
Bristol-Myers Squibb Co. |
Triglyceride and triglyceride-like prodrugs of glycogen phosphorylase inhibiting compounds
|
US20040110241A1
(en)
*
|
2002-12-06 |
2004-06-10 |
Segal Mark S. |
Materials and methods for monitoring vascular endothelial function
|
ES2310676T3
(es)
|
2002-12-20 |
2009-01-16 |
Pfizer Products Inc. |
Formas de dosificacion que comprenden un inhibidor de cetp y un inhibidor de hmg-coa reductasa.
|
US20040132771A1
(en)
*
|
2002-12-20 |
2004-07-08 |
Pfizer Inc |
Compositions of choleseteryl ester transfer protein inhibitors and HMG-CoA reductase inhibitors
|
DE10261067A1
(de)
*
|
2002-12-24 |
2004-08-05 |
Nutrinova Nutrition Specialties & Food Ingredients Gmbh |
Cholesterinsenkendes Mittel, enthaltend eine n-3-Fettsäure
|
DE10261061A1
(de)
*
|
2002-12-24 |
2004-07-15 |
Nutrinova Nutrition Specialties & Food Ingredients Gmbh |
Diätetisches Lebensmittel zur positiven Beeinflussung der kardiovaskulären Gesundheit
|
TW200504021A
(en)
*
|
2003-01-24 |
2005-02-01 |
Bristol Myers Squibb Co |
Substituted anilide ligands for the thyroid receptor
|
WO2004071431A2
(fr)
*
|
2003-02-05 |
2004-08-26 |
Myriad Genetics, Inc. |
Composition et methode de traitement de troubles neurodegeneratifs
|
US20040186046A1
(en)
*
|
2003-03-17 |
2004-09-23 |
Pfizer Inc |
Treatment of type 1 diabetes with PDE5 inhibitors
|
WO2004091626A1
(fr)
*
|
2003-04-07 |
2004-10-28 |
Osteoscreen, Inc. |
Stimulation de la croissance osseuse avec no/statine et autres combinaisons modulatoires
|
US7557143B2
(en)
*
|
2003-04-18 |
2009-07-07 |
Bristol-Myers Squibb Company |
Thyroid receptor ligands
|
US7459474B2
(en)
*
|
2003-06-11 |
2008-12-02 |
Bristol-Myers Squibb Company |
Modulators of the glucocorticoid receptor and method
|
CA2613021A1
(fr)
*
|
2003-06-18 |
2004-12-29 |
Teva Pharmaceutical Industries Ltd |
Forme lxxx de cristaux de fluvastatine sodique, procedes pour les preparer, compositions et methodes pour les utiliser
|
US7368468B2
(en)
*
|
2003-06-18 |
2008-05-06 |
Teva Pharmaceutical Industries Ltd. |
Fluvastatin sodium crystal forms XIV, LXXIII, LXXIX, LXXX and LXXXVII, processes for preparing them, compositions containing them and methods of using them
|
JP2007528857A
(ja)
*
|
2003-07-11 |
2007-10-18 |
ミリアド ジェネティクス, インコーポレイテッド |
アルツハイマー病の処置のための薬学的方法、投与レジメンおよび投薬形態
|
US6995183B2
(en)
|
2003-08-01 |
2006-02-07 |
Bristol Myers Squibb Company |
Adamantylglycine-based inhibitors of dipeptidyl peptidase IV and methods
|
AU2004266740B2
(en)
|
2003-08-21 |
2010-08-26 |
Merck Frosst Canada Ltd |
Cathepsin cysteine protease inhibitors
|
CA2537271A1
(fr)
*
|
2003-08-28 |
2005-03-17 |
Teva Pharmaceutical Industries, Ltd. |
Procede de preparation de sels calciques de rosuvastatine
|
AU2004267972B2
(en)
|
2003-08-29 |
2010-07-08 |
Kowa Co., Ltd. |
Method of stabilizing lipid-rich plaque and method of preventing rupture thereof
|
US20050171207A1
(en)
*
|
2003-09-26 |
2005-08-04 |
Myriad Genetics, Incorporated |
Method and composition for combination treatment of neurodegenerative disorders
|
US7767828B2
(en)
*
|
2003-11-12 |
2010-08-03 |
Phenomix Corporation |
Methyl and ethyl substituted pyrrolidine compounds and methods for selective inhibition of dipeptidyl peptidase-IV
|
US7674913B2
(en)
|
2003-11-12 |
2010-03-09 |
Phenomix Corporation |
Heterocyclic boronic acid compounds
|
US7576121B2
(en)
*
|
2003-11-12 |
2009-08-18 |
Phenomix Corporation |
Pyrrolidine compounds and methods for selective inhibition of dipeptidyl peptidase-IV
|
US7317109B2
(en)
*
|
2003-11-12 |
2008-01-08 |
Phenomix Corporation |
Pyrrolidine compounds and methods for selective inhibition of dipeptidyl peptidase-IV
|
RU2422450C2
(ru)
|
2003-11-19 |
2011-06-27 |
Метабазис Терапеутикс, Инк. |
Новые фосфорсодержащие тиромиметики
|
CA2546701C
(fr)
*
|
2003-11-24 |
2010-07-27 |
Teva Pharmaceutical Industries Ltd. |
Sels d'ammonium cristallins de la rosuvastatine
|
WO2005053683A1
(fr)
*
|
2003-11-26 |
2005-06-16 |
Duke University |
Technique de prevention ou de traitement du glaucome
|
WO2005056534A1
(fr)
*
|
2003-12-02 |
2005-06-23 |
Teva Pharmaceutical Industries Ltd. |
Norme de reference pour la caracterisation de la rosuvastatine
|
CA2550742A1
(fr)
*
|
2003-12-24 |
2005-07-14 |
Teva Pharmaceutical Industries Ltd. |
Procede de preparation de statines a rapport syn anti eleve
|
US20070179166A1
(en)
*
|
2003-12-24 |
2007-08-02 |
Valerie Niddam-Hildesheim |
Process for preparation of statins with high syn to anti ratio
|
US7851624B2
(en)
*
|
2003-12-24 |
2010-12-14 |
Teva Pharamaceutical Industries Ltd. |
Triol form of rosuvastatin and synthesis of rosuvastatin
|
US20070161700A1
(en)
*
|
2004-12-28 |
2007-07-12 |
Kowa Company, Ltd. |
Inhibitor for the formation of y-secretase complex
|
EP1559419A1
(fr)
*
|
2004-01-23 |
2005-08-03 |
Fournier Laboratories Ireland Limited |
Composition pharmaceutique contenant une combinaison de mefformine et d'un fibrate et les procédés pour les obtenir
|
US20100216863A1
(en)
*
|
2004-01-30 |
2010-08-26 |
Decode Genetics Ehf. |
Susceptibility Gene for Myocardial Infarction, Stroke, and PAOD; Methods of Treatment
|
US8158362B2
(en)
*
|
2005-03-30 |
2012-04-17 |
Decode Genetics Ehf. |
Methods of diagnosing susceptibility to myocardial infarction and screening for an LTA4H haplotype
|
EP1563837A1
(fr)
*
|
2004-02-03 |
2005-08-17 |
Ferrer Internacional, S.A. |
Compositions hypocholesterolemiques comprenant une statine et un médicament antiflatulent
|
EP1719525B1
(fr)
*
|
2004-02-25 |
2014-12-10 |
Kowa Company, Ltd. |
Promoteur de transfert nuclaire pour la proteine cdc42 et methode de criblage pour celle-ci
|
US8309574B2
(en)
*
|
2004-02-25 |
2012-11-13 |
Kowa Company, Ltd. |
Nuclear transfer promoter for Rac protein and method of screening the same
|
US20060211752A1
(en)
|
2004-03-16 |
2006-09-21 |
Kohn Leonard D |
Use of phenylmethimazoles, methimazole derivatives, and tautomeric cyclic thiones for the treatment of autoimmune/inflammatory diseases associated with toll-like receptor overexpression
|
US20070293538A1
(en)
*
|
2004-04-13 |
2007-12-20 |
Myriad Genetics, Incorporated |
Pharmaceutical Composition And Methods For Treating Neurodegenerative Disorders
|
KR20070004036A
(ko)
*
|
2004-04-29 |
2007-01-05 |
키스톤 리테이닝 월 시스템스, 아이엔씨 |
벽, 옹벽 및 그 외 유사한 것을 위한 베니어
|
AU2005247195A1
(en)
*
|
2004-05-27 |
2005-12-08 |
Dexcel Pharma Technologies Ltd |
Localized controlled absorption of statins in the gastrointestinal tract for achieving high blood levels of statins
|
UA87854C2
(en)
|
2004-06-07 |
2009-08-25 |
Мерк Энд Ко., Инк. |
N-(2-benzyl)-2-phenylbutanamides as androgen receptor modulators
|
US7145040B2
(en)
*
|
2004-07-02 |
2006-12-05 |
Bristol-Myers Squibb Co. |
Process for the preparation of amino acids useful in the preparation of peptide receptor modulators
|
TW200611704A
(en)
*
|
2004-07-02 |
2006-04-16 |
Bristol Myers Squibb Co |
Human glucagon-like-peptide-1 modulators and their use in the treatment of diabetes and related conditions
|
US7534763B2
(en)
|
2004-07-02 |
2009-05-19 |
Bristol-Myers Squibb Company |
Sustained release GLP-1 receptor modulators
|
WO2006017292A1
(fr)
*
|
2004-07-12 |
2006-02-16 |
Phenomix Corporation |
Composes cyano contraints
|
JP2007508379A
(ja)
*
|
2004-07-13 |
2007-04-05 |
テバ ファーマシューティカル インダストリーズ リミティド |
Tempo媒介型酸化段階を包含するロスバスタチンの調製方法
|
US7572805B2
(en)
|
2004-07-14 |
2009-08-11 |
Bristol-Myers Squibb Company |
Pyrrolo(oxo)isoquinolines as 5HT ligands
|
US20090042979A1
(en)
*
|
2004-08-06 |
2009-02-12 |
Transform Pharmaceuticals Inc. |
Novel Statin Pharmaceutical Compositions and Related Methods of Treatment
|
KR20070052760A
(ko)
*
|
2004-08-06 |
2007-05-22 |
트렌스폼 파마수티컬스 인코퍼레이티드 |
신규한 페노피브레이트 제제 및 관련된 치료방법
|
KR20070038553A
(ko)
*
|
2004-08-06 |
2007-04-10 |
트렌스폼 파마수티컬스 인코퍼레이티드 |
신규한 스타틴 약제학적 조성물 및 관련된 치료방법
|
WO2006020852A2
(fr)
*
|
2004-08-11 |
2006-02-23 |
Myriad Genetics, Inc. |
Composition pharmaceutique et technique de traitement de troubles neurodegeneratifs
|
WO2006020853A2
(fr)
*
|
2004-08-11 |
2006-02-23 |
Myriad Genetics, Inc. |
Composition pharmaceutique et methode de traitement de troubles neurodegeneratifs
|
WO2006020850A2
(fr)
*
|
2004-08-11 |
2006-02-23 |
Myriad Genetics, Inc. |
Composition pharmaceutique et technique de traitement de troubles neurodegeneratifs
|
AR051446A1
(es)
*
|
2004-09-23 |
2007-01-17 |
Bristol Myers Squibb Co |
Glucosidos de c-arilo como inhibidores selectivos de transportadores de glucosa (sglt2)
|
US7517991B2
(en)
*
|
2004-10-12 |
2009-04-14 |
Bristol-Myers Squibb Company |
N-sulfonylpiperidine cannabinoid receptor 1 antagonists
|
CA2584740A1
(fr)
*
|
2004-10-19 |
2006-04-27 |
Cargill, Incorporated |
Systemes de production de viande
|
EP1817010A4
(fr)
*
|
2004-11-22 |
2009-06-17 |
Dexcel Pharma Technologies Ltd |
Absorption maitrisee de statines dans l'intestin
|
AU2005314230B2
(en)
|
2004-12-09 |
2011-05-19 |
Merck Sharp & Dohme Corp. |
Estrogen receptor modulators
|
TW200619204A
(en)
*
|
2004-12-10 |
2006-06-16 |
Kowa Co |
Method for reduction, stabilization and prevention of rupture of lipid rich plaque
|
US7635699B2
(en)
*
|
2004-12-29 |
2009-12-22 |
Bristol-Myers Squibb Company |
Azolopyrimidine-based inhibitors of dipeptidyl peptidase IV and methods
|
US7589088B2
(en)
*
|
2004-12-29 |
2009-09-15 |
Bristol-Myers Squibb Company |
Pyrimidine-based inhibitors of dipeptidyl peptidase IV and methods
|
US7361766B2
(en)
|
2005-01-12 |
2008-04-22 |
Bristol-Myers Squibb Company |
Bicyclic heterocycles as cannabinoid receptor modulators
|
WO2006076598A2
(fr)
*
|
2005-01-12 |
2006-07-20 |
Bristol-Myers Squibb Company |
Composes heterocycliques bicycliques en tant que modulateurs des recepteurs de canabinoides
|
WO2006076597A1
(fr)
*
|
2005-01-12 |
2006-07-20 |
Bristol-Myers Squibb Company |
Heterocycles bicycliques constituant des modulateurs des recepteurs cannabinoides
|
WO2006078697A1
(fr)
*
|
2005-01-18 |
2006-07-27 |
Bristol-Myers Squibb Company |
Heterocycles bicycliques utilises comme modulateurs des recepteurs de cannabinoide
|
US7238702B2
(en)
*
|
2005-02-10 |
2007-07-03 |
Bristol-Myers Squibb Company |
Dihydroquinazolinones as 5HT modulators
|
US20070167625A1
(en)
*
|
2005-02-22 |
2007-07-19 |
Anna Balanov |
Preparation of rosuvastatin
|
US20070037979A1
(en)
*
|
2005-02-22 |
2007-02-15 |
Valerie Niddam-Hildesheim |
Preparation of rosuvastatin
|
KR100945763B1
(ko)
|
2005-02-22 |
2010-03-08 |
테바 파마슈티컬 인더스트리즈 리미티드 |
로수바스타틴의 제조 방법
|
US20070293535A1
(en)
*
|
2005-02-24 |
2007-12-20 |
Kowa Company, Ltd. |
Nuclear Transfer Promoter for Ddc42 Protein and Method of Screening the Dame
|
JP2008531691A
(ja)
|
2005-03-02 |
2008-08-14 |
メルク エンド カムパニー インコーポレーテッド |
カテプシンk阻害組成物
|
EP1863449A2
(fr)
*
|
2005-03-28 |
2007-12-12 |
Dexcel Pharma Technologies Ltd. |
Absorption regulee de statines dans l'intestin
|
US20060235028A1
(en)
|
2005-04-14 |
2006-10-19 |
Li James J |
Inhibitors of 11-beta hydroxysteroid dehydrogenase type I
|
ES2382814T3
(es)
|
2005-05-17 |
2012-06-13 |
Merck Sharp & Dohme Ltd. |
Ácido cis-4-[(4-clorofenil)sulfonil]-4-(2,5-difluorofenil)ciclohexanopropanoico para el tratamiento del cáncer
|
US7521557B2
(en)
|
2005-05-20 |
2009-04-21 |
Bristol-Myers Squibb Company |
Pyrrolopyridine-based inhibitors of dipeptidyl peptidase IV and methods
|
US7825139B2
(en)
*
|
2005-05-25 |
2010-11-02 |
Forest Laboratories Holdings Limited (BM) |
Compounds and methods for selective inhibition of dipeptidyl peptidase-IV
|
PE20061448A1
(es)
*
|
2005-05-26 |
2006-12-17 |
Bristol Myers Squibb Co |
Compuestos polipeptidos como moduladores del peptido 1 similar al glucagon humano
|
US7452892B2
(en)
*
|
2005-06-17 |
2008-11-18 |
Bristol-Myers Squibb Company |
Triazolopyrimidine cannabinoid receptor 1 antagonists
|
US7317012B2
(en)
*
|
2005-06-17 |
2008-01-08 |
Bristol-Myers Squibb Company |
Bicyclic heterocycles as cannabinoind-1 receptor modulators
|
US7629342B2
(en)
*
|
2005-06-17 |
2009-12-08 |
Bristol-Myers Squibb Company |
Azabicyclic heterocycles as cannabinoid receptor modulators
|
US20060287342A1
(en)
*
|
2005-06-17 |
2006-12-21 |
Mikkilineni Amarendra B |
Triazolopyrimidine heterocycles as cannabinoid receptor modulators
|
US7632837B2
(en)
*
|
2005-06-17 |
2009-12-15 |
Bristol-Myers Squibb Company |
Bicyclic heterocycles as cannabinoid-1 receptor modulators
|
US7572808B2
(en)
*
|
2005-06-17 |
2009-08-11 |
Bristol-Myers Squibb Company |
Triazolopyridine cannabinoid receptor 1 antagonists
|
CA2615063A1
(fr)
*
|
2005-07-22 |
2007-02-01 |
Myriad Genetics, Inc. |
Formes posologiques et preparations a charge medicamenteuse elevee
|
CA2617102A1
(fr)
*
|
2005-07-28 |
2007-02-08 |
Bristol-Myers Squibb Company |
Tetrahydro-1h-pyrido[4,3,b]indoles substitues utilises en tant qu'agonistes et antagonistes des recepteurs de la serotonine
|
BRPI0614378A2
(pt)
*
|
2005-08-04 |
2011-03-22 |
Transform Pharmaceuticals Inc |
formulações compreendendo fenofibrato e uma estatina, e métodos de tratamento relacionados
|
CA2619576C
(fr)
*
|
2005-08-16 |
2011-12-06 |
Teva Pharmaceutical Industries Ltd. |
Intermediaire de rosuvastatine sous forme cristalline
|
US7795436B2
(en)
*
|
2005-08-24 |
2010-09-14 |
Bristol-Myers Squibb Company |
Substituted tricyclic heterocycles as serotonin receptor agonists and antagonists
|
EP1919393A2
(fr)
*
|
2005-09-01 |
2008-05-14 |
Prescient Medical, Inc. |
Medicaments enrobant un dispositif destine a traiter une plaque vulnerable
|
WO2007035395A2
(fr)
*
|
2005-09-16 |
2007-03-29 |
Virginia Commonwealth University Intellectual Property Foundation |
Compositions therapeutiques comprenant des gonadotropines chorioniques et des inhibiteurs de la reductase hmg coa
|
DE102005049293A1
(de)
*
|
2005-10-15 |
2007-04-26 |
Bayer Healthcare Ag |
Kombinationspräparate von Salzen oder o-Acetylsalicylsäure
|
US7741317B2
(en)
|
2005-10-21 |
2010-06-22 |
Bristol-Myers Squibb Company |
LXR modulators
|
US8618115B2
(en)
|
2005-10-26 |
2013-12-31 |
Bristol-Myers Squibb Company |
Substituted thieno[3,2-d]pyrimidinones as MCHR1 antagonists and methods for using them
|
EP2487154B1
(fr)
|
2005-10-31 |
2013-10-16 |
Bristol-Myers Squibb Company |
Inhibiteurs de la dipeptidyl peptidase IV à base amide de bêta-amino de pyrrolidinyle et procédés
|
US7888376B2
(en)
|
2005-11-23 |
2011-02-15 |
Bristol-Myers Squibb Company |
Heterocyclic CETP inhibitors
|
US7592461B2
(en)
|
2005-12-21 |
2009-09-22 |
Bristol-Myers Squibb Company |
Indane modulators of glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof
|
WO2007082264A2
(fr)
*
|
2006-01-11 |
2007-07-19 |
Bristol-Myers Squibb Company |
Modulateurs de peptides 1 de type glucagon humain et leur utilisation pour traiter le diabète et des états associés
|
US7553836B2
(en)
*
|
2006-02-06 |
2009-06-30 |
Bristol-Myers Squibb Company |
Melanin concentrating hormone receptor-1 antagonists
|
US8367112B2
(en)
*
|
2006-02-28 |
2013-02-05 |
Alkermes Pharma Ireland Limited |
Nanoparticulate carverdilol formulations
|
US20070238770A1
(en)
*
|
2006-04-05 |
2007-10-11 |
Bristol-Myers Squibb Company |
Process for preparing novel crystalline forms of peliglitazar, novel stable forms produced therein and formulations
|
EP2573111A1
(fr)
|
2006-04-20 |
2013-03-27 |
Amgen Inc. |
Composés GLP-1
|
US7659281B2
(en)
*
|
2006-04-25 |
2010-02-09 |
Bristol-Myers Squibb Company |
HMG-CoA reductase inhibitors
|
WO2007139589A1
(fr)
|
2006-05-26 |
2007-12-06 |
Bristol-Myers Squibb Company |
Modulateurs des récepteurs de glp-1 à libération prolongée
|
US7919598B2
(en)
|
2006-06-28 |
2011-04-05 |
Bristol-Myers Squibb Company |
Crystal structures of SGLT2 inhibitors and processes for preparing same
|
US20080044326A1
(en)
*
|
2006-07-04 |
2008-02-21 |
Esencia Co., Ltd. |
Sterilizer for baby products
|
US20080033045A1
(en)
*
|
2006-07-07 |
2008-02-07 |
Myriad Genetics, Incorporated |
Treatment of psychiatric disorders
|
US7727978B2
(en)
|
2006-08-24 |
2010-06-01 |
Bristol-Myers Squibb Company |
Cyclic 11-beta hydroxysteroid dehydrogenase type I inhibitors
|
US20080161324A1
(en)
*
|
2006-09-14 |
2008-07-03 |
Johansen Lisa M |
Compositions and methods for treatment of viral diseases
|
US20080118572A1
(en)
*
|
2006-10-10 |
2008-05-22 |
Harold Richard Hellstrom |
Methods and compositions for reducing the risk of adverse cardiovascular events associated with the administration of artificial blood
|
US20100055173A1
(en)
*
|
2006-10-10 |
2010-03-04 |
Adel Penhasi |
Release of statins in the intestine
|
US20110218176A1
(en)
|
2006-11-01 |
2011-09-08 |
Barbara Brooke Jennings-Spring |
Compounds, methods, and treatments for abnormal signaling pathways for prenatal and postnatal development
|
WO2008057862A2
(fr)
|
2006-11-01 |
2008-05-15 |
Bristol-Myers Squibb Company |
Modulateurs de récepteur de glucocorticoïde, d'activité ap-1 et/ou nf-κb, et leur utilisation
|
TW200904405A
(en)
|
2007-03-22 |
2009-02-01 |
Bristol Myers Squibb Co |
Pharmaceutical formulations containing an SGLT2 inhibitor
|
TWI407955B
(zh)
|
2007-03-29 |
2013-09-11 |
Kowa Co |
高脂血症之預防及/或治療劑
|
US8546394B2
(en)
|
2007-04-17 |
2013-10-01 |
Bristol-Myers Squibb Company |
Substituted [1,2,4]triazolo[4,3-A]pyrazine 11-beta-hydroxysteroid dehydrogenase inhibitors
|
PE20090696A1
(es)
|
2007-04-20 |
2009-06-20 |
Bristol Myers Squibb Co |
Formas cristalinas de saxagliptina y procesos para preparar las mismas
|
JP2010528023A
(ja)
*
|
2007-05-18 |
2010-08-19 |
ブリストル−マイヤーズ スクイブ カンパニー |
Sglt2阻害剤の結晶構造およびその製造方法
|
AU2008287542C1
(en)
|
2007-06-01 |
2015-01-22 |
The Trustees Of Princeton University |
Treatment of viral infections by modulation of host cell metabolic pathways
|
US20090011994A1
(en)
*
|
2007-07-06 |
2009-01-08 |
Bristol-Myers Squibb Company |
Non-basic melanin concentrating hormone receptor-1 antagonists and methods
|
ES2408384T3
(es)
*
|
2007-07-27 |
2013-06-20 |
Bristol-Myers Squibb Company |
Nuevos activadores de glucoquinasa y procedimientos de uso de los mismos
|
WO2009058944A2
(fr)
|
2007-11-01 |
2009-05-07 |
Bristol-Myers Squibb Company |
Composés non stéroïdiens utiles en tant que modulateurs de l'activité ap-1 et/ou nf-κb du récepteur des glucocorticoïdes et leur utilisation
|
US20090163452A1
(en)
*
|
2007-12-20 |
2009-06-25 |
Schwartz Janice B |
Compositions and methods for lowering serum cholesterol
|
US8354446B2
(en)
|
2007-12-21 |
2013-01-15 |
Ligand Pharmaceuticals Incorporated |
Selective androgen receptor modulators (SARMs) and uses thereof
|
PE20091928A1
(es)
*
|
2008-05-29 |
2009-12-31 |
Bristol Myers Squibb Co |
Tienopirimidinas hidroxisustituidas como antagonistas de receptor-1 de hormona concentradora de melanina no basicos
|
US20120046364A1
(en)
|
2009-02-10 |
2012-02-23 |
Metabasis Therapeutics, Inc. |
Novel Sulfonic Acid-Containing Thyromimetics, and Methods for Their Use
|
US20100256153A1
(en)
|
2009-03-27 |
2010-10-07 |
Bristol-Myers Squibb Company |
Methods for preventing or reducing risk of mortality
|
EP2413932A4
(fr)
|
2009-04-01 |
2012-09-19 |
Merck Sharp & Dohme |
Inhibiteurs de l'activité akt
|
US8470805B2
(en)
*
|
2009-04-30 |
2013-06-25 |
Kaohsiung Medical University |
Processes for preparing piperazinium salts of KMUP and use thereof
|
LT2435410T
(lt)
|
2009-05-28 |
2017-04-10 |
Exelixis Patent Company Llc |
Lxr moduliatoriai
|
EP2488028B1
(fr)
|
2009-10-14 |
2020-08-19 |
Merck Sharp & Dohme Corp. |
Pipéridines substituées qui accroissent l'activité de p53 et utilisations de ces composés
|
EP2498757A1
(fr)
|
2009-11-13 |
2012-09-19 |
Bristol-Myers Squibb Company |
Formulations de metformine a masse reduite
|
CN102711739B
(zh)
|
2009-11-13 |
2015-12-16 |
阿斯利康(瑞典)有限公司 |
双层片剂
|
BR112012011733A2
(pt)
|
2009-11-13 |
2019-09-24 |
Bristol-Myers Squibb Company |
formulações de comprimido de liberação imediata
|
AR079336A1
(es)
*
|
2009-12-11 |
2012-01-18 |
Irm Llc |
Antagonistas de la pro-proteina convertasa-subtilisina/quexina tipo 9 (pcsk9)
|
TWI562775B
(en)
|
2010-03-02 |
2016-12-21 |
Lexicon Pharmaceuticals Inc |
Methods of using inhibitors of sodium-glucose cotransporters 1 and 2
|
ES2559209T3
(es)
|
2010-04-14 |
2016-02-11 |
Bristol-Myers Squibb Company |
Nuevos activadores de la glucocinasa y métodos de uso de los mismos
|
US8372877B2
(en)
|
2010-04-16 |
2013-02-12 |
Cumberland Pharmaceuticals |
Stabilized statin formulations
|
EP2571860A1
(fr)
|
2010-05-21 |
2013-03-27 |
Pfizer Inc |
2-phénylbenzoylamides
|
EP2584903B1
(fr)
|
2010-06-24 |
2018-10-24 |
Merck Sharp & Dohme Corp. |
Nouveaux composés hétérocycliques utilisés comme inhibiteurs de erk
|
JP6042330B2
(ja)
|
2010-07-09 |
2016-12-14 |
ビーエイチヴィ ファーマ、インコーポレイテッド |
レモグリフロジンを含めた半減期が短い医薬品のための組合せ即時/遅延放出送達システム
|
US8946216B2
(en)
|
2010-09-01 |
2015-02-03 |
Merck Sharp & Dohme Corp. |
Indazole derivatives useful as ERK inhibitors
|
US9242981B2
(en)
|
2010-09-16 |
2016-01-26 |
Merck Sharp & Dohme Corp. |
Fused pyrazole derivatives as novel ERK inhibitors
|
KR20130137623A
(ko)
|
2010-10-06 |
2013-12-17 |
고쿠리츠다이가쿠호우진 도쿄다이가쿠 |
림프 부종 예방 치료제
|
TWI462739B
(zh)
|
2010-11-02 |
2014-12-01 |
Univ Kaohsiung Medical |
Sildenafil-同族物四級銨哌嗪鹽類之製備及醫療用途
|
WO2012087772A1
(fr)
|
2010-12-21 |
2012-06-28 |
Schering Corporation |
Dérivés d'indazole utiles en tant qu'inhibiteurs de erk
|
TWI631963B
(zh)
|
2011-01-05 |
2018-08-11 |
雷西肯製藥股份有限公司 |
包含鈉-葡萄糖共同輸送體1與2之抑制劑的組合物與應用方法
|
US8791162B2
(en)
|
2011-02-14 |
2014-07-29 |
Merck Sharp & Dohme Corp. |
Cathepsin cysteine protease inhibitors
|
EP2680874A2
(fr)
|
2011-03-04 |
2014-01-08 |
Pfizer Inc |
Peptides de type edn3 et utilisations associées
|
AR088728A1
(es)
|
2011-03-25 |
2014-07-02 |
Bristol Myers Squibb Co |
Moduladores de lxr como prodroga de imidazol
|
US8586527B2
(en)
|
2011-10-20 |
2013-11-19 |
Jaipal Singh |
Cerivastatin to treat pulmonary disorders
|
EP2770987B1
(fr)
|
2011-10-27 |
2018-04-04 |
Merck Sharp & Dohme Corp. |
Nouveaux composés qui sont des inhibiteurs d'erk
|
KR101466617B1
(ko)
|
2011-11-17 |
2014-11-28 |
한미약품 주식회사 |
오메가-3 지방산 및 HMG-CoA 환원효소 억제제를 포함하는 안정성이 증가된 경구용 복합 제제
|
US20150010630A1
(en)
|
2011-12-29 |
2015-01-08 |
Trustees Of Tufts College |
Functionalization of biomaterials to control regeneration and inflammation responses
|
US8729092B2
(en)
*
|
2012-09-24 |
2014-05-20 |
Terence J. Scallen |
Rosuvastatin enantiomer compounds
|
WO2014052563A2
(fr)
|
2012-09-28 |
2014-04-03 |
Merck Sharp & Dohme Corp. |
Nouveaux composés inhibiteurs de erk
|
JP6278971B2
(ja)
|
2012-11-20 |
2018-02-14 |
レクシコン ファーマシューティカルズ インコーポレイテッド |
ナトリウムグルコース共輸送体1の阻害剤
|
CA2892361A1
(fr)
|
2012-11-28 |
2014-06-05 |
Merck Sharp & Dohme Corp. |
Utilisation d'un inhibiteur wee1 pour traiter un cancer caracterise par de faibles niveaux d'expression de proteines tyrosine et threonine kinases 1 (pkmyt1) associee a la membrane
|
AU2013361694B2
(en)
|
2012-12-20 |
2017-10-26 |
Merck Sharp & Dohme Corp. |
Substituted imidazopyridines as HDM2 inhibitors
|
WO2014120748A1
(fr)
|
2013-01-30 |
2014-08-07 |
Merck Sharp & Dohme Corp. |
Purines 2,6,7,8-substituées utilisées en tant qu'inhibiteurs de hdm2
|
WO2014144037A1
(fr)
|
2013-03-15 |
2014-09-18 |
Bristol-Myers Squibb Company |
Modulateurs des lxr
|
EP2986599A1
(fr)
|
2013-04-17 |
2016-02-24 |
Pfizer Inc. |
Dérivés de n-pipéridin-3-ylbenzamide dans le traitement des maladies cardiovasculaires
|
WO2015027021A1
(fr)
|
2013-08-22 |
2015-02-26 |
Bristol-Myers Squibb Company |
Dérivés imide et acylurée utilisés comme modulateurs du récepteur de glucocorticoïdes
|
WO2015054089A1
(fr)
|
2013-10-08 |
2015-04-16 |
Merck Sharp & Dohme Corp. |
Inhibiteurs de protéases à cystéine de type cathepsines
|
WO2015051479A1
(fr)
|
2013-10-08 |
2015-04-16 |
Merck Sharp & Dohme Corp. |
Inhibiteurs de cystéine-protéases de type cathepsines
|
WO2015108988A2
(fr)
|
2014-01-17 |
2015-07-23 |
Ligand Pharmaceuticals, Inc. |
Méthodes et compositions pour moduler les taux d'hormone
|
WO2015120580A1
(fr)
|
2014-02-11 |
2015-08-20 |
Merck Sharp & Dohme Corp. |
Inhibiteurs de protéases à cystéine de type cathépsines
|
WO2015181676A1
(fr)
|
2014-05-30 |
2015-12-03 |
Pfizer Inc. |
Dérivés carbonitriles en tant que modulateurs sélectifs du récepteur des androgènes
|
CA2958898A1
(fr)
|
2014-09-15 |
2016-03-24 |
The Board Of Trustees Of The Leland Stanford Junior University |
Ciblage d'une maladie anevrismale par des voies de modulation de la phagocytose
|
WO2016055901A1
(fr)
|
2014-10-08 |
2016-04-14 |
Pfizer Inc. |
Composés d'amide substitué
|
EP4218812A1
(fr)
|
2015-02-27 |
2023-08-02 |
The Board of Trustees of the Leland Stanford Junior University |
Polythérapie pour le traitement de l'atherosclérose
|
WO2016176656A2
(fr)
|
2015-04-30 |
2016-11-03 |
President And Fellows Of Harvard College |
Anticorps anti-ap2 et agents de liaison à l'antigène utilisables en vue du traitement d'affections métaboliques
|
EP3706742B1
(fr)
|
2017-11-08 |
2023-03-15 |
Merck Sharp & Dohme LLC |
Inhibiteurs de prmt5
|
US11981701B2
(en)
|
2018-08-07 |
2024-05-14 |
Merck Sharp & Dohme Llc |
PRMT5 inhibitors
|
WO2020033282A1
(fr)
|
2018-08-07 |
2020-02-13 |
Merck Sharp & Dohme Corp. |
Inhibiteurs de prmt5
|
MX2021003545A
(es)
|
2018-09-26 |
2021-05-27 |
Lexicon Pharmaceuticals Inc |
Formas solidas cristalinas de n-(1-((2-(dimetilamino)etil)amino)-2 -metil-1-oxopropan-2-il)-4-(4-(2-metil-5-((2s,3r,4r,5s,6r)-3,4,5- trihidroxi-6-(metiltio)tetrahidro-2h-piran-2-il)bencil)fenil)buta namida y metodos para su sintesis.
|
CA3125765A1
(fr)
|
2019-01-18 |
2020-07-23 |
Astrazeneca Ab |
Inhibiteurs de pcsk9 et leurs procedes d'utilisation
|
CA3160153A1
(fr)
|
2019-12-17 |
2021-06-24 |
Michelle Machacek |
Inhibiteurs de prmt5
|
WO2023275715A1
(fr)
|
2021-06-30 |
2023-01-05 |
Pfizer Inc. |
Métabolites de modulateurs sélectifs du récepteur des androgènes
|