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
|
EP0705837B1
(fr)
*
|
1994-09-06 |
2002-08-07 |
Ube Industries, Ltd. |
Préparation de derivés de l'acide 3-oxy-5-oxo-6-heptènoique
|
NZ332313A
(en)
|
1996-04-16 |
2000-02-28 |
Bayer Ag |
D-mannitol and its preparation as a powder of not more than 1 square meter per gram
|
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
|
US6432931B1
(en)
|
1998-06-24 |
2002-08-13 |
Merck & Co., Inc. |
Compositions and methods for inhibiting bone resorption
|
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
|
AU5702201A
(en)
*
|
2000-04-13 |
2001-10-30 |
Mayo Foundation |
Abeta<sub>42</sub> lowering agents
|
US6627636B2
(en)
|
2000-06-15 |
2003-09-30 |
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
|
US6812345B2
(en)
|
2000-06-15 |
2004-11-02 |
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
|
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
|
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
|
JPWO2002030425A1
(ja)
*
|
2000-10-12 |
2004-02-19 |
日産化学工業株式会社 |
糖尿病合併症予防・治療剤
|
JO2409B1
(en)
|
2000-11-21 |
2007-06-17 |
شركة جانسين فارماسوتيكا ان. في |
Second-phenyl carboxy amides are useful as lipid-lowering agents
|
EP1345903A1
(fr)
*
|
2000-12-21 |
2003-09-24 |
Ciba SC Holding AG |
Formes cristallines de sodium de cerivastatine
|
JO2390B1
(en)
|
2001-04-06 |
2007-06-17 |
شركة جانسين فارماسوتيكا ان. في |
Diphenylcarboxamides act as lipid-lowering agents
|
AU2002254567B2
(en)
|
2001-04-11 |
2007-10-11 |
Bristol-Myers Squibb Company |
Amino acid complexes of C-aryl glucosides for treatment of diabetes and method
|
MXPA03009562A
(es)
*
|
2001-04-18 |
2004-02-12 |
Genzyme Corp |
METODO PARA TRATAR EL SiNDROME X CON POLIAMINAS ALIFATICAS.
|
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
|
KR20040026705A
(ko)
*
|
2001-08-16 |
2004-03-31 |
테바 파마슈티컬 인더스트리즈 리미티드 |
스타틴의 칼슘 염 형태의 제조 방법
|
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
|
HUP0700151A2
(en)
*
|
2001-10-18 |
2007-05-29 |
Bristol Myers Squibb Co |
Human glucagon-like-peptide-1 mimics and their use in the treatment of diabetes and related conditions
|
US6806381B2
(en)
*
|
2001-11-02 |
2004-10-19 |
Bristol-Myers Squibb Company |
Process for the preparation of aniline-derived thyroid receptor ligands
|
AU2002348276A1
(en)
*
|
2001-11-16 |
2003-06-10 |
Bristol-Myers Squibb Company |
Dual inhibitors of adipocyte fatty acid binding protein and keratinocyte fatty acid binding protein
|
US6831102B2
(en)
*
|
2001-12-07 |
2004-12-14 |
Bristol-Myers Squibb Company |
Phenyl naphthol ligands for thyroid hormone receptor
|
US7482366B2
(en)
|
2001-12-21 |
2009-01-27 |
X-Ceptor Therapeutics, Inc. |
Modulators of LXR
|
ES2367539T3
(es)
*
|
2001-12-21 |
2011-11-04 |
X-Ceptor Therapeutics, Inc. |
Moduladores heterocíclicos de receptores nucleares.
|
ES2421511T3
(es)
*
|
2001-12-21 |
2013-09-03 |
X Ceptor Therapeutics Inc |
Moduladores de LXR
|
IL163666A0
(en)
|
2002-02-22 |
2005-12-18 |
New River Pharmaceuticals Inc |
Active agent delivery systems and methods for protecting and administering active agents
|
WO2003088900A2
(fr)
*
|
2002-04-16 |
2003-10-30 |
Merck & Co., Inc. |
Formes solides de sels a activite tyrosine kinase
|
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
|
CN100471047C
(zh)
*
|
2002-05-14 |
2009-03-18 |
西门子公司 |
用于产生发射信号的方法
|
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
|
CA2493645A1
(fr)
*
|
2002-07-23 |
2004-01-29 |
Nutrinova Nutrition Specialties & Food Ingredients Gmbh |
Agent hypocholesterolemiant constitue de fibres alimentaires et de substances hypocholesterolemiantes
|
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
|
ES2344057T3
(es)
*
|
2002-10-23 |
2010-08-17 |
Bristol-Myers Squibb Company |
Inhibidores de la dipeptidil peptidasa iv basados en nitrilos de glicina.
|
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
|
DE60331873D1
(de)
|
2002-12-20 |
2010-05-06 |
Pfizer Prod Inc |
Dosierungsform enthaltend einen CETP-Hemmer und einen HMG-CoA Reduktase Hemmer
|
US20040132771A1
(en)
*
|
2002-12-20 |
2004-07-08 |
Pfizer Inc |
Compositions of choleseteryl ester transfer protein inhibitors and HMG-CoA reductase inhibitors
|
DE10261061A1
(de)
*
|
2002-12-24 |
2004-07-15 |
Nutrinova Nutrition Specialties & Food Ingredients Gmbh |
Diätetisches Lebensmittel zur positiven Beeinflussung der kardiovaskulären Gesundheit
|
DE10261067A1
(de)
*
|
2002-12-24 |
2004-08-05 |
Nutrinova Nutrition Specialties & Food Ingredients Gmbh |
Cholesterinsenkendes Mittel, enthaltend eine n-3-Fettsäure
|
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
|
US20040254238A1
(en)
*
|
2003-04-07 |
2004-12-16 |
Osteoscreen |
Bone growth stimulation with NO/statin and other NO modulating combinations
|
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
|
EP1790635A3
(fr)
*
|
2003-06-18 |
2007-06-13 |
Teva Pharmaceutical Industries, Inc. |
Procédés de préparation de sodium de fluvastatine amorphe
|
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
|
AU2004311577A1
(en)
*
|
2003-07-11 |
2005-07-21 |
Myriad Genetics, Inc. |
Pharmaceutical methods, dosing regimes and dosage forms for the treatment of Alzheimer's disease
|
US6995183B2
(en)
*
|
2003-08-01 |
2006-02-07 |
Bristol Myers Squibb Company |
Adamantylglycine-based inhibitors of dipeptidyl peptidase IV and methods
|
EP1673336B1
(fr)
|
2003-08-21 |
2014-06-04 |
Merck Canada Inc. |
Inhibiteurs de cathepsine et de cysteine protease
|
WO2005023778A2
(fr)
*
|
2003-08-28 |
2005-03-17 |
Teva Pharmaceutical Industries Ltd. |
Procede de preparation de sels calciques de rosuvastatine
|
JPWO2005020996A1
(ja)
|
2003-08-29 |
2007-11-01 |
興和株式会社 |
リピド・リッチ・プラークの安定化方法及び破裂予防方法
|
US20050171207A1
(en)
*
|
2003-09-26 |
2005-08-04 |
Myriad Genetics, Incorporated |
Method and composition for combination treatment of neurodegenerative disorders
|
PL1689757T3
(pl)
*
|
2003-11-12 |
2015-05-29 |
Sino Med Int Alliance Inc |
Heterocykliczne związki kwasu boronowego
|
US7576121B2
(en)
*
|
2003-11-12 |
2009-08-18 |
Phenomix Corporation |
Pyrrolidine compounds and methods for selective inhibition of dipeptidyl peptidase-IV
|
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
|
US7317109B2
(en)
*
|
2003-11-12 |
2008-01-08 |
Phenomix Corporation |
Pyrrolidine compounds and methods for selective inhibition of dipeptidyl peptidase-IV
|
WO2005051298A2
(fr)
|
2003-11-19 |
2005-06-09 |
Metabasis Therapeutics, Inc. |
Nouvelles substances thyromimetiques contenant du phosphore
|
TW200526596A
(en)
*
|
2003-11-24 |
2005-08-16 |
Teva Pharma |
Crystalline ammonium salts of rosuvastatin
|
EP1722780A4
(fr)
*
|
2003-11-26 |
2008-12-17 |
Univ Duke |
Technique de prevention ou de traitement du glaucome
|
CA2546894C
(fr)
*
|
2003-12-02 |
2009-09-08 |
Teva Pharmaceutical Industries Ltd. |
Norme de reference pour la caracterisation de la rosuvastatine
|
EP1697338A2
(fr)
*
|
2003-12-24 |
2006-09-06 |
Teva Pharmaceutical Industries Ltd. |
Procede de preparation de statines a rapport syn anti eleve
|
US7851624B2
(en)
*
|
2003-12-24 |
2010-12-14 |
Teva Pharamaceutical Industries Ltd. |
Triol form of rosuvastatin and synthesis of rosuvastatin
|
US20070179166A1
(en)
*
|
2003-12-24 |
2007-08-02 |
Valerie Niddam-Hildesheim |
Process for preparation of statins with high syn to anti ratio
|
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
|
US8158362B2
(en)
*
|
2005-03-30 |
2012-04-17 |
Decode Genetics Ehf. |
Methods of diagnosing susceptibility to myocardial infarction and screening for an LTA4H haplotype
|
US20100216863A1
(en)
*
|
2004-01-30 |
2010-08-26 |
Decode Genetics Ehf. |
Susceptibility Gene for Myocardial Infarction, Stroke, and PAOD; Methods of Treatment
|
EP1563837A1
(fr)
*
|
2004-02-03 |
2005-08-17 |
Ferrer Internacional, S.A. |
Compositions hypocholesterolemiques comprenant une statine et un médicament antiflatulent
|
EP1719524B1
(fr)
*
|
2004-02-25 |
2014-11-26 |
Kowa Company, Ltd. |
AGENT PROMOTEUR DE TRANSFERT NUCLEAIRE POUR LA PROTINE Rac ET METHODE POUR LA CRIBLER
|
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
|
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
|
WO2006001877A2
(fr)
*
|
2004-04-13 |
2006-01-05 |
Myriad Genetics, Inc. |
Composition pharmaceutique et methode de traitement de troubles neurodegeneratifs
|
US20050252144A1
(en)
*
|
2004-04-29 |
2005-11-17 |
Macdonald Robert A |
Veneers for walls, retaining walls and the like
|
EP1748761A4
(fr)
*
|
2004-05-27 |
2011-10-12 |
Dexcel Pharma Technologies Ltd |
Absorption regulee et localisee de statines dans le tractus gastro-intestinal aux fins de l'obtention de taux sanguins eleves de statines
|
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
|
EP1778220A1
(fr)
*
|
2004-07-12 |
2007-05-02 |
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
|
BRPI0514189A
(pt)
*
|
2004-08-06 |
2008-06-03 |
Transform Pharmaceuticals Inc |
composições farmacêuticas de estatina e métodos de tratamento relacionados
|
US20090149533A1
(en)
*
|
2004-08-06 |
2009-06-11 |
Transform Pharmaceuticals, Inc. |
Novel fenofibrate formulations and related methods of treatment
|
US20090042979A1
(en)
*
|
2004-08-06 |
2009-02-12 |
Transform Pharmaceuticals Inc. |
Novel Statin Pharmaceutical Compositions and Related Methods of Treatment
|
WO2006020850A2
(fr)
*
|
2004-08-11 |
2006-02-23 |
Myriad Genetics, Inc. |
Composition pharmaceutique et technique de traitement de troubles neurodegeneratifs
|
BRPI0514303A
(pt)
*
|
2004-08-11 |
2008-06-10 |
Myriad Genetics Inc |
composição farmacêutica e método para tratar distúrbios neurodegenerativos
|
WO2006020852A2
(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
|
CA2588215A1
(fr)
*
|
2004-11-22 |
2006-05-26 |
Dexcel Pharma Technologies Ltd. |
Absorption maitrisee de statines dans l'intestin
|
WO2006062876A2
(fr)
|
2004-12-09 |
2006-06-15 |
Merck & Co., Inc. |
Modulateurs du recepteur de l'oestrogene
|
TW200619204A
(en)
*
|
2004-12-10 |
2006-06-16 |
Kowa Co |
Method for reduction, stabilization and prevention of rupture of lipid rich plaque
|
US7589088B2
(en)
*
|
2004-12-29 |
2009-09-15 |
Bristol-Myers Squibb Company |
Pyrimidine-based inhibitors of dipeptidyl peptidase IV and methods
|
US7635699B2
(en)
*
|
2004-12-29 |
2009-12-22 |
Bristol-Myers Squibb Company |
Azolopyrimidine-based inhibitors of dipeptidyl peptidase IV and methods
|
US7368458B2
(en)
*
|
2005-01-12 |
2008-05-06 |
Bristol-Myers Squibb Company |
Bicyclic heterocycles as cannabinoid receptor modulators
|
WO2006076568A2
(fr)
|
2005-01-12 |
2006-07-20 |
Bristol-Myers Squibb Company |
Heterocycles bicycliques servant de modulateurs au recepteur de cannabinoides
|
WO2006076598A2
(fr)
*
|
2005-01-12 |
2006-07-20 |
Bristol-Myers Squibb Company |
Composes heterocycliques bicycliques en tant que modulateurs des recepteurs de canabinoides
|
WO2006078697A1
(fr)
*
|
2005-01-18 |
2006-07-27 |
Bristol-Myers Squibb Company |
Heterocycles bicycliques utilises comme modulateurs des recepteurs de cannabinoide
|
WO2006086464A2
(fr)
*
|
2005-02-10 |
2006-08-17 |
Bristol-Myers Squibb Company |
Dihydroquinazolinones utilisees comme modulateurs de la 5ht
|
TWI353981B
(en)
*
|
2005-02-22 |
2011-12-11 |
Teva Pharma |
Preparation of rosuvastatin
|
US20070037979A1
(en)
*
|
2005-02-22 |
2007-02-15 |
Valerie Niddam-Hildesheim |
Preparation of rosuvastatin
|
US20070167625A1
(en)
*
|
2005-02-22 |
2007-07-19 |
Anna Balanov |
Preparation of rosuvastatin
|
US20070293535A1
(en)
*
|
2005-02-24 |
2007-12-20 |
Kowa Company, Ltd. |
Nuclear Transfer Promoter for Ddc42 Protein and Method of Screening the Dame
|
EP1855674B1
(fr)
|
2005-03-02 |
2014-07-16 |
Merck Sharp & Dohme Corp. |
Composition destinee a l'inhibition de cathepsine k
|
US20080260818A1
(en)
*
|
2005-03-28 |
2008-10-23 |
Dexcel Pharma Technologies Ltd. |
Controlled Absorption of Statins in the Intestine
|
EP1879881A2
(fr)
|
2005-04-14 |
2008-01-23 |
Bristol-Myers Squibb Company |
Inhibiteurs de la 11-beta hydroxysteroide deshydrogenase de type i
|
ATE550019T1
(de)
|
2005-05-17 |
2012-04-15 |
Merck Sharp & Dohme |
Cis-4-ä(4-chlorophenyl)sulfonylü-4-(2,5- difluorophenyl)cyclohexanepropansäure zur behandlug von krebs
|
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
|
AR053495A1
(es)
*
|
2005-05-26 |
2007-05-09 |
Bristol Myers Squibb Co |
Moduladores del peptido 1 similar al glucagon humano y su uso en el tratamiento de la diabetes y condiciones relacionadas
|
TW200726765A
(en)
*
|
2005-06-17 |
2007-07-16 |
Bristol Myers Squibb Co |
Triazolopyridine cannabinoid receptor 1 antagonists
|
US7632837B2
(en)
*
|
2005-06-17 |
2009-12-15 |
Bristol-Myers Squibb Company |
Bicyclic heterocycles as cannabinoid-1 receptor modulators
|
US20060287342A1
(en)
*
|
2005-06-17 |
2006-12-21 |
Mikkilineni Amarendra B |
Triazolopyrimidine heterocycles as cannabinoid receptor modulators
|
US7317012B2
(en)
*
|
2005-06-17 |
2008-01-08 |
Bristol-Myers Squibb Company |
Bicyclic heterocycles as cannabinoind-1 receptor modulators
|
US7452892B2
(en)
*
|
2005-06-17 |
2008-11-18 |
Bristol-Myers Squibb Company |
Triazolopyrimidine cannabinoid receptor 1 antagonists
|
US7629342B2
(en)
*
|
2005-06-17 |
2009-12-08 |
Bristol-Myers Squibb Company |
Azabicyclic heterocycles as cannabinoid receptor modulators
|
CA2615063A1
(fr)
*
|
2005-07-22 |
2007-02-01 |
Myriad Genetics, Inc. |
Formes posologiques et preparations a charge medicamenteuse elevee
|
AU2006275694A1
(en)
*
|
2005-07-28 |
2007-02-08 |
Bristol-Myers Squibb Company |
Substituted tetrahydro-1H-pyrido(4,3,b)indoles as serotonin receptor agonists and antagonists
|
RU2008108078A
(ru)
*
|
2005-08-04 |
2009-09-10 |
Трансформ Фармасьютикалз, Инк. (Us) |
Новые препаративные формы, включающие фенофибрат и статин, и соответствующие способы лечения
|
JP2008515931A
(ja)
*
|
2005-08-16 |
2008-05-15 |
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 |
結晶形ロスバスタチン中間体
|
US7795436B2
(en)
*
|
2005-08-24 |
2010-09-14 |
Bristol-Myers Squibb Company |
Substituted tricyclic heterocycles as serotonin receptor agonists and antagonists
|
WO2007030302A2
(fr)
*
|
2005-09-01 |
2007-03-15 |
Prescient Medical, Inc. |
Medicaments enrobant un dispositif destine a traiter une plaque vulnerable
|
US20080139457A1
(en)
*
|
2005-09-16 |
2008-06-12 |
Virginia Commonwealth University |
Therapeutic compositions comprising chorionic gonadotropins and HMG CoA reductase inhibitors
|
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
|
AR056155A1
(es)
|
2005-10-26 |
2007-09-19 |
Bristol Myers Squibb Co |
Antagonistas del receptor 1 de la hormona de concentracion de melanina no basica
|
WO2007053819A2
(fr)
|
2005-10-31 |
2007-05-10 |
Bristol-Myers Squibb Company |
Inhibiteurs à base d'amide et de bêta-amino de pyrrolidinyle de la dipeptidyl peptidase iv 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
|
US8288339B2
(en)
|
2006-04-20 |
2012-10-16 |
Amgen Inc. |
GLP-1 compounds
|
US7659281B2
(en)
*
|
2006-04-25 |
2010-02-09 |
Bristol-Myers Squibb Company |
HMG-CoA reductase inhibitors
|
US20100022457A1
(en)
*
|
2006-05-26 |
2010-01-28 |
Bristol-Myers Squibb Company |
Sustained release glp-1 receptor modulators
|
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
|
WO2008033466A2
(fr)
*
|
2006-09-14 |
2008-03-20 |
Combinatorx (Singapore) Pre. Ltd. |
Compositions et procédés pour le traitement de maladies virales
|
EP2079448A2
(fr)
*
|
2006-10-10 |
2009-07-22 |
Dexcel Pharma Technologies Ltd. |
Libération améliorée de statines dans l'intestin
|
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
|
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
|
PE20090185A1
(es)
|
2007-03-22 |
2009-02-28 |
Bristol Myers Squibb Co |
Formulaciones farmaceuticas que contienen un inhibidor sglt2
|
TWI407955B
(zh)
|
2007-03-29 |
2013-09-11 |
Kowa Co |
高脂血症之預防及/或治療劑
|
EP2142551B1
(fr)
|
2007-04-17 |
2015-10-14 |
Bristol-Myers Squibb Company |
Composés HÉTÉROCYCLIQUEs CONDENSÉS comme INHIBITEURS DE la 11-béta-HYDROXYSTÉROÏDE DÉSHYDROGÉNASE DE TYPE I
|
PE20090696A1
(es)
|
2007-04-20 |
2009-06-20 |
Bristol Myers Squibb Co |
Formas cristalinas de saxagliptina y procesos para preparar las mismas
|
CN101754972A
(zh)
*
|
2007-05-18 |
2010-06-23 |
百时美施贵宝公司 |
Sglt2抑制剂的晶体结构及其制备方法
|
JP5616220B2
(ja)
|
2007-06-01 |
2014-10-29 |
ザ トラスティーズ オブ プリンストン ユニバーシティ |
宿主細胞代謝経路の調節によるウイルス感染治療
|
US20090011994A1
(en)
*
|
2007-07-06 |
2009-01-08 |
Bristol-Myers Squibb Company |
Non-basic melanin concentrating hormone receptor-1 antagonists and methods
|
JP2010534722A
(ja)
*
|
2007-07-27 |
2010-11-11 |
ブリストル−マイヤーズ スクイブ カンパニー |
新規グルコキナーゼ活性化薬およびその使用方法
|
ES2448839T3
(es)
|
2007-11-01 |
2014-03-17 |
Bristol-Myers Squibb Company |
Compuestos no esteroideos útiles como moderadores de la actividad del receptor de glucocorticoides AP-1 y/o NF-kappa b y uso de los mismos
|
US20090163452A1
(en)
*
|
2007-12-20 |
2009-06-25 |
Schwartz Janice B |
Compositions and methods for lowering serum cholesterol
|
EP2489656A1
(fr)
|
2007-12-21 |
2012-08-22 |
Ligand Pharmaceuticals Inc. |
Modulateurs de récepteurs androgènes sélectifs (sarm) et leurs utilisations
|
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
|
EA201101231A1
(ru)
|
2009-03-27 |
2012-06-29 |
Бристол-Майерс Сквибб Компани |
Способы предотвращения или снижения риска смертности
|
WO2010114780A1
(fr)
|
2009-04-01 |
2010-10-07 |
Merck Sharp & Dohme Corp. |
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
|
JP5625050B2
(ja)
|
2009-05-28 |
2014-11-12 |
エグゼリクシス パテント カンパニー エルエルシー |
Lxrの調節因子
|
BR112012008849A2
(pt)
|
2009-10-14 |
2015-09-22 |
Schering Corp |
composto, composição farmacêutica, e, uso de um composto
|
PT2498758T
(pt)
|
2009-11-13 |
2018-10-23 |
Astrazeneca Uk Ltd |
Formulações de comprimido bicamada
|
MX2012005425A
(es)
|
2009-11-13 |
2012-06-14 |
Astrazeneca Uk Ltd |
Formulaciones de metformina de masa reducida.
|
CA2780941C
(fr)
|
2009-11-13 |
2018-06-12 |
Bristol-Myers Squibb Company |
Formulations pour comprimes a liberation immediate
|
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
|
US8592396B2
(en)
|
2010-04-14 |
2013-11-26 |
Bristol-Myers Squibb Company |
Glucokinase activators and methods of using same
|
US8372877B2
(en)
|
2010-04-16 |
2013-02-12 |
Cumberland Pharmaceuticals |
Stabilized statin formulations
|
JP2013528172A
(ja)
|
2010-05-21 |
2013-07-08 |
ファイザー・インク |
2−フェニルベンゾイルアミド
|
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
|
WO2012030685A2
(fr)
|
2010-09-01 |
2012-03-08 |
Schering Corporation |
Dérivés d'indazole utilisables en tant qu'inhibiteurs de la voie erk
|
EP2615916B1
(fr)
|
2010-09-16 |
2017-01-04 |
Merck Sharp & Dohme Corp. |
Dérivés condensés de pyrazole utilisés comme nouveaux inhibiteurs erk
|
CN103153299A
(zh)
|
2010-10-06 |
2013-06-12 |
国立大学法人东京大学 |
淋巴水肿预防治疗剂
|
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
|
EP2675440B1
(fr)
|
2011-02-14 |
2020-03-25 |
Merck Sharp & Dohme Corp. |
Inhibiteurs de cystéine protéases, les cathepsines
|
JP2014513923A
(ja)
|
2011-03-04 |
2014-06-19 |
ファイザー・インク |
Edn3様ペプチドおよびその使用
|
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
|
WO2013102193A1
(fr)
|
2011-12-29 |
2013-07-04 |
Trustees Of Tufts College |
Fonctionnalisation de biomatériaux pour commander la régénération et des réponses à une inflammation
|
US8729092B2
(en)
*
|
2012-09-24 |
2014-05-20 |
Terence J. Scallen |
Rosuvastatin enantiomer compounds
|
JP6280554B2
(ja)
|
2012-09-28 |
2018-02-14 |
メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. |
Erk阻害剤である新規化合物
|
CA2891773C
(fr)
|
2012-11-20 |
2021-01-19 |
Lexicon Pharmaceuticals, Inc. |
Inhibiteurs du cotransporteur sodium glucose 1
|
PL2925888T3
(pl)
|
2012-11-28 |
2018-03-30 |
Merck Sharp & Dohme Corp. |
Kompozycje i sposoby do stosowania w leczeniu nowotworów
|
WO2014100065A1
(fr)
|
2012-12-20 |
2014-06-26 |
Merck Sharp & Dohme Corp. |
Imidazopyridines substituées en tant qu'inhibiteurs de hdm2
|
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
|
CN105209039B
(zh)
|
2013-03-15 |
2018-06-22 |
百时美施贵宝公司 |
Lxr调节剂
|
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
|
CN105593230B
(zh)
|
2013-10-08 |
2018-07-06 |
默沙东公司 |
组织蛋白酶半胱氨酸蛋白酶抑制剂
|
WO2015051479A1
(fr)
|
2013-10-08 |
2015-04-16 |
Merck Sharp & Dohme Corp. |
Inhibiteurs de cystéine-protéases de type cathepsines
|
US10441567B2
(en)
|
2014-01-17 |
2019-10-15 |
Ligand Pharmaceuticals Incorporated |
Methods and compositions for modulating hormone levels
|
WO2015120580A1
(fr)
|
2014-02-11 |
2015-08-20 |
Merck Sharp & Dohme Corp. |
Inhibiteurs de protéases à cystéine de type cathépsines
|
KR20160147007A
(ko)
|
2014-05-30 |
2016-12-21 |
화이자 인코포레이티드 |
선택적인 안드로겐 수용체 조절제로서의 카보니트릴 유도체
|
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
|
ES2838925T3
(es)
|
2015-02-27 |
2021-07-02 |
Univ Leland Stanford Junior |
Terapia de combinación para el tratamiento de la ateroesclerosis
|
MX2017013807A
(es)
|
2015-04-30 |
2018-03-15 |
Harvard College |
Anticuerpos anti-proteina de union al lipido de adipocito humana (ap2) y agente de union al antigeno para tratar trastornos metabolicos.
|
US10975084B2
(en)
|
2016-10-12 |
2021-04-13 |
Merck Sharp & Dohme Corp. |
KDM5 inhibitors
|
CA3063439A1
(fr)
|
2017-05-30 |
2018-12-06 |
The Board Of Trustees Of The Leland Stanford Junior University |
Traitement d'une maladie neuro-inflammatoire
|
US10947234B2
(en)
|
2017-11-08 |
2021-03-16 |
Merck Sharp & Dohme Corp. |
PRMT5 inhibitors
|
US11993602B2
(en)
|
2018-08-07 |
2024-05-28 |
Merck Sharp & Dohme Llc |
PRMT5 inhibitors
|
WO2020033284A1
(fr)
|
2018-08-07 |
2020-02-13 |
Merck Sharp & Dohme Corp. |
Inhibiteurs de prmt5
|
BR112021004839A2
(pt)
|
2018-09-26 |
2021-06-08 |
Lexicon Pharmaceuticals, Inc. |
formas 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-triidróxi-6-(metiltio)tetraidro-2h-piran-2-il)benzil)fenil)butanamida e métodos de sua síntese
|
BR112021013807A2
(pt)
|
2019-01-18 |
2021-11-30 |
Astrazeneca Ab |
Inibidores de pcsk9 e seus métodos de uso
|
BR112022012032A2
(pt)
|
2019-12-17 |
2022-09-06 |
Merck Sharp & Dohme Llc |
Inibidores de prmt5
|
WO2023275715A1
(fr)
|
2021-06-30 |
2023-01-05 |
Pfizer Inc. |
Métabolites de modulateurs sélectifs du récepteur des androgènes
|