CY1115462T1 - ΣΥΝΔΥΑΣΜΟΣ ΑΝΑΣΤΟΛΕΩΝ ΗΜG-CoΑ ΑΝΑΓΩΓΑΣΗΣ ΑΤΟΡΒΑΣΤΑΤΙΝΗΣ Ή ΣYΜΒΑΣΤΑΤΙΝΗΣ ΜΕ ΑΝΑΣΤΟΛΕΑ ΦΩΣΦΟΔΙΕΣΤΕΡΑΣΗΣ 4 ΟΠΩΣ ΡΟΦΛΟΥΜΙΛΑΣΤΗ ΓΙΑ ΤΗ ΘΕΡΑΠΕΙΑ ΦΛΕΓΜΟΝΩΔΩΝ ΠΝΕΥΜΟΝΙΚΩΝ ΑΣΘΕΝΕΙΩΝ - Google Patents

ΣΥΝΔΥΑΣΜΟΣ ΑΝΑΣΤΟΛΕΩΝ ΗΜG-CoΑ ΑΝΑΓΩΓΑΣΗΣ ΑΤΟΡΒΑΣΤΑΤΙΝΗΣ Ή ΣYΜΒΑΣΤΑΤΙΝΗΣ ΜΕ ΑΝΑΣΤΟΛΕΑ ΦΩΣΦΟΔΙΕΣΤΕΡΑΣΗΣ 4 ΟΠΩΣ ΡΟΦΛΟΥΜΙΛΑΣΤΗ ΓΙΑ ΤΗ ΘΕΡΑΠΕΙΑ ΦΛΕΓΜΟΝΩΔΩΝ ΠΝΕΥΜΟΝΙΚΩΝ ΑΣΘΕΝΕΙΩΝ

Info

Publication number
CY1115462T1
CY1115462T1 CY20141100621T CY141100621T CY1115462T1 CY 1115462 T1 CY1115462 T1 CY 1115462T1 CY 20141100621 T CY20141100621 T CY 20141100621T CY 141100621 T CY141100621 T CY 141100621T CY 1115462 T1 CY1115462 T1 CY 1115462T1
Authority
CY
Cyprus
Prior art keywords
coa
roflionimon
atomvastatin
anastoleis
hgg
Prior art date
Application number
CY20141100621T
Other languages
English (en)
Inventor
Stefan-Lutz Wollin
Andrea Wohlsen
Clemens Braun
Degenhard Marx
Original Assignee
Takeda Gmbh
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
Application filed by Takeda Gmbh filed Critical Takeda Gmbh
Publication of CY1115462T1 publication Critical patent/CY1115462T1/el

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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/21Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A61K31/22Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/275Nitriles; Isonitriles
    • A61K31/277Nitriles; Isonitriles having a ring, e.g. verapamil
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/343Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/365Lactones
    • A61K31/366Lactones having six-membered rings, e.g. delta-lactones
    • 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
    • A61K31/405Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4425Pyridinium derivatives, e.g. pralidoxime, pyridostigmine
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/453Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with oxygen as a ring hetero atom
    • 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/502Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/04Drugs for disorders of the respiratory system for throat disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives

Landscapes

  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Pulmonology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Emergency Medicine (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Otolaryngology (AREA)
  • Cardiology (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)

Abstract

Η εφεύρεση αφορά στην συνδυασμένη χρήση ενός αναστολέα ΡDΕ4 με έναν αναστολέα ΗΜG-CoΑ αναγωγάσης για την προληπτική και θεραπευτική αγωγή μιας φλεγμονώδους πνευμονικής ασθένειας.
CY20141100621T 2006-07-05 2014-08-07 ΣΥΝΔΥΑΣΜΟΣ ΑΝΑΣΤΟΛΕΩΝ ΗΜG-CoΑ ΑΝΑΓΩΓΑΣΗΣ ΑΤΟΡΒΑΣΤΑΤΙΝΗΣ Ή ΣYΜΒΑΣΤΑΤΙΝΗΣ ΜΕ ΑΝΑΣΤΟΛΕΑ ΦΩΣΦΟΔΙΕΣΤΕΡΑΣΗΣ 4 ΟΠΩΣ ΡΟΦΛΟΥΜΙΛΑΣΤΗ ΓΙΑ ΤΗ ΘΕΡΑΠΕΙΑ ΦΛΕΓΜΟΝΩΔΩΝ ΠΝΕΥΜΟΝΙΚΩΝ ΑΣΘΕΝΕΙΩΝ CY1115462T1 (el)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP06116625 2006-07-05
EP11164518.0A EP2363130B1 (en) 2006-07-05 2007-07-03 Combination of HMG-CoA reductase inhibitors atorvastatin or simvastatin with a phosphodiesterase 4 inhibitor, such as roflumilast for the treatment of inflammatory pulmonary diseases

Publications (1)

Publication Number Publication Date
CY1115462T1 true CY1115462T1 (el) 2017-01-04

Family

ID=37311957

Family Applications (2)

Application Number Title Priority Date Filing Date
CY20141100008T CY1114742T1 (el) 2006-07-05 2014-01-07 Συνδυασμος του αναστολεα αναγωγασης ημg-coa ροζουβαστατινης με αναστολεα φωσφοδιεστερασης 4, οπως η ροφλουμιλαστη, ν-οξειδιο ροφλουμιλαστης για τη θεραπεια φλεγμονωδων πνευμονικων νοσων
CY20141100621T CY1115462T1 (el) 2006-07-05 2014-08-07 ΣΥΝΔΥΑΣΜΟΣ ΑΝΑΣΤΟΛΕΩΝ ΗΜG-CoΑ ΑΝΑΓΩΓΑΣΗΣ ΑΤΟΡΒΑΣΤΑΤΙΝΗΣ Ή ΣYΜΒΑΣΤΑΤΙΝΗΣ ΜΕ ΑΝΑΣΤΟΛΕΑ ΦΩΣΦΟΔΙΕΣΤΕΡΑΣΗΣ 4 ΟΠΩΣ ΡΟΦΛΟΥΜΙΛΑΣΤΗ ΓΙΑ ΤΗ ΘΕΡΑΠΕΙΑ ΦΛΕΓΜΟΝΩΔΩΝ ΠΝΕΥΜΟΝΙΚΩΝ ΑΣΘΕΝΕΙΩΝ

Family Applications Before (1)

Application Number Title Priority Date Filing Date
CY20141100008T CY1114742T1 (el) 2006-07-05 2014-01-07 Συνδυασμος του αναστολεα αναγωγασης ημg-coa ροζουβαστατινης με αναστολεα φωσφοδιεστερασης 4, οπως η ροφλουμιλαστη, ν-οξειδιο ροφλουμιλαστης για τη θεραπεια φλεγμονωδων πνευμονικων νοσων

Country Status (26)

Country Link
US (2) US20100069392A1 (el)
EP (3) EP2040707B1 (el)
JP (3) JP5349302B2 (el)
KR (1) KR101433394B1 (el)
CN (3) CN101484166B (el)
AT (1) ATE535244T1 (el)
AU (1) AU2007271186C1 (el)
BR (1) BRPI0713768A2 (el)
CA (1) CA2656366A1 (el)
CY (2) CY1114742T1 (el)
DK (2) DK2359826T3 (el)
EA (2) EA032476B1 (el)
ES (3) ES2378281T3 (el)
HR (2) HRP20140073T1 (el)
IL (3) IL195433A (el)
ME (2) ME01901B (el)
MX (1) MX2008016123A (el)
NO (1) NO342590B1 (el)
NZ (3) NZ594369A (el)
PL (2) PL2363130T3 (el)
PT (2) PT2363130E (el)
RS (2) RS53084B (el)
SI (2) SI2359826T1 (el)
UA (3) UA101556C2 (el)
WO (1) WO2008003701A2 (el)
ZA (1) ZA200809905B (el)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ587591A (en) * 2008-03-14 2012-10-26 Otsuka Pharma Co Ltd Diarylthiazole derivatives such as tetomilast as mmp-2 and/or mmp-9 inhibitors
CN102671198A (zh) * 2011-12-17 2012-09-19 东莞达信生物技术有限公司 一种降压降脂复方药及其制备方法
JP6755240B2 (ja) * 2014-06-05 2020-09-16 トランスゲニオン−インターナショナル インスティテュート フォー リジェネレイティヴ トランスレイショナル メディシン ゲーエムベーハー 新規分子バイオマーカーを使用して慢性閉塞性肺疾患(copd)を診断する方法
EP3152329A2 (en) 2014-06-05 2017-04-12 Transregion-International Institute For Translational Medicine Gmbh Methods of diagnosing chronic obstructive pulmonary disease (copd) using novel molecular biomarkers
WO2015185656A1 (en) * 2014-06-05 2015-12-10 Medizinische Universität Wien Methods of diagnosing chronic obstructive pulmonary disease (copd) using novel molecular biomarkers
US20210031012A1 (en) 2018-01-26 2021-02-04 Progenity, Inc. Treatment of a disease of the gastrointestinal tract with a pde4 inhibitor
KR20210095165A (ko) 2018-11-19 2021-07-30 프로제너티, 인크. 바이오의약품으로 질환을 치료하기 위한 방법 및 디바이스
EP4309722A2 (en) 2019-12-13 2024-01-24 Biora Therapeutics, Inc. Ingestible device for delivery of therapeutic agent to the gastrointestinal tract
WO2021218988A1 (zh) * 2020-04-30 2021-11-04 中国科学院上海药物研究所 Prdx1激动剂及其用途
US20240042147A1 (en) * 2022-08-03 2024-02-08 Chiesi Farmaceutici S.P.A. Dry powder inhaler

Family Cites Families (60)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU535944B2 (en) 1979-06-15 1984-04-12 Merck & Co., Inc. Hypocholestermic fermentation products from aspergillus
AU548996B2 (en) 1980-02-04 1986-01-09 Merck & Co., Inc. Tetrahydro-2h-pyran-2-one derivatives
DK149080C (da) * 1980-06-06 1986-07-28 Sankyo Co Fremgangsmaade til fremstilling af derivater af ml-236b-carboxylsyre
WO1984002131A1 (en) 1982-11-22 1984-06-07 Sandoz Ag Analogs of mevalolactone and derivatives thereof, processes for their production, pharmaceutical compositions containing them and their use as pharmaceuticals
US4681893A (en) 1986-05-30 1987-07-21 Warner-Lambert Company Trans-6-[2-(3- or 4-carboxamido-substituted pyrrol-1-yl)alkyl]-4-hydroxypyran-2-one inhibitors of cholesterol synthesis
EP0307342B1 (de) 1987-07-10 1996-01-03 Hoechst Aktiengesellschaft 3-Desmethyl-mevalonsäurederivate, Verfahren zu ihrer Herstellung, pharmazeutische Präparate auf Basis dieser Verbindungen, ihre Verwendung sowie Zwischenprodukte
CA1336714C (en) 1987-08-20 1995-08-15 Yoshihiro Fujikawa Quinoline type mevalonolactone inhibitors of cholesterol biosynthesis
US4863957A (en) 1987-12-21 1989-09-05 Rorer Pharmaceutical Corporation Novel HMG-CoA reductase inhibitors
FR2642065B1 (fr) 1989-01-24 1991-05-24 Lipha Derives d'acides benzocycloalcenyl dihydroxy alcanoiques, procede de preparation et medicaments les contenant
JP2829451B2 (ja) 1990-11-30 1998-11-25 大塚製薬株式会社 活性酸素抑制剤
JP2648897B2 (ja) 1991-07-01 1997-09-03 塩野義製薬株式会社 ピリミジン誘導体
WO1993019749A1 (en) 1992-04-02 1993-10-14 Smithkline Beecham Corporation Compounds useful for treating allergic and inflammatory diseases
RO115872B1 (ro) * 1992-04-02 2000-07-28 Smithkline Beecham Corp Derivati substituiti ai acidului fenilcarboxilic si compozitie farmaceutica ce ii contine
DK0706513T3 (da) 1993-07-02 2002-09-09 Altana Pharma Ag Fluoralkoxysubstituerede benzamider og anvendelse deraf som cyklisk-nukleotid phosphodiesteraseinhibitorer
GB9504460D0 (en) 1995-03-06 1995-04-26 Bayer Ag N-(3-Benzofuranyl)urea-derivatives
DK0837860T3 (da) 1995-06-06 2002-05-27 Pfizer Tricykliske 5,6-dihydro-9H-pyrazolo[3,4-c]-1,2,4-triazolo-[4,3-alfa]pyridiner
DE19636150A1 (de) 1996-09-06 1998-03-12 Asta Medica Ag N-substituierte Indol-3-glyoxylamide mit antiasthmatischer, antiallergischer und immunsuppressiver/immunmodulierender Wirkung
ES2262072T3 (es) 1998-04-28 2006-11-16 Elbion Ag Derivados de indol y su utilizacion como inhibidores de la fosfodiesterasa 4.
US20010006656A1 (en) 1999-02-17 2001-07-05 University Of Washington Methods and compositions for inhibiting inflammation associated with pulmonary disease
DE19944161A1 (de) 1999-09-15 2001-03-22 Bayer Ag Neue Kombination zur Behandlung von sexueller Dysfunktion
US6410563B1 (en) * 1999-12-22 2002-06-25 Merck Frosst Canada & Co. Substituted 8-arylquinoline phosphodiesterase-4 inhibitors
MY134008A (en) 1999-12-22 2007-11-30 Merck Frosst Canada Inc Subtituted 8-arylquinoline phospohodiestrase-4 inhibitors
JP2001294526A (ja) * 2000-02-10 2001-10-23 Takeda Chem Ind Ltd TNF−α抑制剤
US20030018040A1 (en) 2000-02-10 2003-01-23 Yasuo Sugiyama Tnf-alpha inhibitors
MY123585A (en) 2000-03-23 2006-05-31 Merck Canada Inc Tri-aryl-substituted-ethane pde4 inhibitors.
US20050102317A1 (en) * 2000-07-21 2005-05-12 Ali Kamarei System and method for event calendaring using a customizable rules subset
AU2002210521A1 (en) 2000-09-19 2002-04-02 Novimmune S.A. Use of statins (HMG-CoA reductase inhibitors) for the preparation of medicament as a novel type of immunomodulator, immunosuppressor and anti-inflammatory agent
US6740666B2 (en) * 2000-12-20 2004-05-25 Merck & Co., Inc. Substituted 8-arylquinoline phosphodiesterase-4 inhibitors
AU2002234634B2 (en) * 2001-02-15 2007-07-26 Takeda Gmbh Phthalayinone-piperidino-derivatives as PDE4 inhibitors
IL157734A0 (en) * 2001-03-06 2004-03-28 Cellegy Pharma Inc Pharmaceutical compositions for the treatment of urogenital disorders
JP4193435B2 (ja) * 2002-07-23 2008-12-10 ブラザー工業株式会社 インクカートリッジ、および、そのインク充填方法
DE60205899T2 (de) * 2001-05-24 2006-06-29 Merck Frosst Canada & Co, Kirkland 1-biaryl-1,8-naphthyridin-4-one als phosphodieseterase-inhibitoren
DE60204463T2 (de) * 2001-06-27 2006-05-18 Merck Frosst Canada & Co, Kirkland Substituierte 8-Arylchinoline als PDE4-Hemmer
US20030114469A1 (en) 2001-09-27 2003-06-19 Cohen David Saul Combinations
MY140561A (en) 2002-02-20 2009-12-31 Nycomed Gmbh Dosage form containing pde 4 inhibitor as active ingredient
JP2005538972A (ja) * 2002-07-02 2005-12-22 メルク フロスト カナダ アンド カンパニー ジアリール置換エタンピリドンpde4阻害剤
MXPA05005161A (es) * 2002-11-18 2005-07-22 Celgene Corp Metodos de utilizacion y composiciones que comprenden (-)3- (3, 4-dimetoxi- fenil)-3 -(1-oxo -1, 3-dihidro- isoindol- 2-il)- propionamida.
IS7839A (is) 2002-11-22 2004-05-23 Merck Frosst Canada Ltd. 4-oxó-1-(3-setið fenýl-1,4-díhýdró-1,8-naftýridín-3-karboxamíð fosfódíesterasa-4 hindrar
BR0316451A (pt) * 2002-11-27 2005-10-11 Altana Pharma Ag Combinação sinergìstica compreendendo roflumilast e formoterol
US20050119330A1 (en) 2003-03-17 2005-06-02 Kao Peter N. Use of antiproliferative agents in the treatment and prevention of pulmonary proliferative vascular diseases
WO2004091626A1 (en) * 2003-04-07 2004-10-28 Osteoscreen, Inc. Bone growth stimulation with no/statin and other no modulating combinations
KR20060017494A (ko) 2003-04-11 2006-02-23 그렌마크 파머수티칼스 에스. 아. 염증 및 알레르기성 질환 치료용으로 유용한 신규 헤테로사이클릭 화합물, 이의 제조방법 및 이를 함유하는 약학 조성물
EP1635829A1 (en) * 2003-04-30 2006-03-22 Merck Frosst Canada Ltd. 8-(3-biaryl)phenylquinoline phosphodiesterase-4-inhibitors
WO2004098578A2 (en) * 2003-05-12 2004-11-18 Altana Pharma Ag Composition comprising a pde4 inhibitor and a tnf-alfa antagonist selected from infliximab, adalimumab, cdp870 and cdp517
AU2004241749B2 (en) * 2003-05-22 2010-03-25 Takeda Gmbh Composition comprising a PDE4 inhibitor and a PDE5 inhibitor
US20060160834A1 (en) * 2003-06-06 2006-07-20 Fong Tung M Combination therapy for the treatment of hypertension
US20060148721A1 (en) * 2003-06-06 2006-07-06 Erondu Ngozi E Combination therapy for the treatment of dyslipidemia
DE10348646A1 (de) 2003-10-15 2005-05-25 Gkn Driveline International Gmbh Rollbalg mit großem Krümmungsradius
AU2005235306B2 (en) * 2004-04-19 2008-08-21 Loma Linda University Composition and method of decreasing renal ischemic damage
CA2563377A1 (en) * 2004-04-23 2005-11-03 Celgene Corporation Methods of using and compositions comprising pde4 modulators for the treatment and management of pulmonary hypertension
ES2257152B1 (es) * 2004-05-31 2007-07-01 Laboratorios Almirall S.A. Combinaciones que comprenden agentes antimuscarinicos y agonistas beta-adrenergicos.
GB0415789D0 (en) * 2004-07-15 2004-08-18 Astrazeneca Ab Novel combination
DE102004046236A1 (de) 2004-09-22 2006-03-30 Altana Pharma Ag Arzneimittelzubereitung
GB0508924D0 (en) 2005-04-30 2005-06-08 Astrazeneca Ab New use
GB0510207D0 (en) 2005-05-19 2005-06-22 Astrazeneca Ab Novel combination
ES2362534T3 (es) 2005-06-08 2011-07-07 Kowa Company, Ltd. Nuevo agente reductor de los triglicéridos.
EP2377530A3 (en) * 2005-10-21 2012-06-20 Braincells, Inc. Modulation of neurogenesis by PDE inhibition
AR057555A1 (es) * 2005-10-27 2007-12-05 Merck Frosst Canada Ltd Un inhibidor de fosfodiesterasa-4 4-oxo-1-(3-sustituido fenil-1,4-dihidro-1,8-naftiridin-3-carboxamida y un procedimiento de preparacion del mismo
WO2007054896A1 (en) 2005-11-08 2007-05-18 Ranbaxy Laboratories Limited Process for (3r, 5r)-7-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4- [(4-hydroxy methyl phenyl amino) carbonyl]-pyrrol-1-yl]-3, 5-dihydroxy-heptanoic acid hemi calcium salt
WO2008036846A2 (en) * 2006-09-22 2008-03-27 Braincells, Inc. Combination comprising an hmg-coa reductase inhibitor and a second neurogenic agent for treating a nervous system disorder and increasing neurogenesis

Also Published As

Publication number Publication date
EP2359826A1 (en) 2011-08-24
NZ603207A (en) 2013-12-20
CY1114742T1 (el) 2016-12-14
IL195433A (en) 2013-02-28
US20100069392A1 (en) 2010-03-18
EP2363130A1 (en) 2011-09-07
BRPI0713768A2 (pt) 2012-10-30
PT2359826E (pt) 2014-01-20
ES2489265T3 (es) 2014-09-01
UA101556C2 (uk) 2013-04-10
WO2008003701A2 (en) 2008-01-10
UA98466C2 (uk) 2012-05-25
AU2007271186C1 (en) 2013-08-15
NZ573378A (en) 2012-03-30
JP2009541459A (ja) 2009-11-26
EA032476B1 (ru) 2019-06-28
HRP20140073T1 (hr) 2014-02-28
PT2363130E (pt) 2014-06-25
ME01901B (me) 2014-12-20
US9713614B2 (en) 2017-07-25
HRP20140707T1 (hr) 2014-09-12
IL221307A (en) 2014-08-31
DK2363130T3 (da) 2014-07-21
EP2363130B1 (en) 2014-05-07
WO2008003701A3 (en) 2008-03-13
MX2008016123A (es) 2009-01-15
EA200900073A1 (ru) 2009-06-30
JP2013035870A (ja) 2013-02-21
EP2040707A2 (en) 2009-04-01
JP5349302B2 (ja) 2013-11-20
CN101484166A (zh) 2009-07-15
ZA200809905B (en) 2009-11-25
KR20090025368A (ko) 2009-03-10
NO342590B1 (no) 2018-06-18
PL2363130T3 (pl) 2014-09-30
CN102764440A (zh) 2012-11-07
CN102772411A (zh) 2012-11-14
PL2359826T3 (pl) 2014-04-30
AU2007271186B2 (en) 2013-01-17
JP2013035871A (ja) 2013-02-21
SI2363130T1 (sl) 2014-09-30
IL221307A0 (en) 2012-09-24
ATE535244T1 (de) 2011-12-15
AU2007271186A1 (en) 2008-01-10
DK2359826T3 (da) 2014-01-20
NO20090370L (no) 2009-02-04
EP2040707B1 (en) 2011-11-30
CA2656366A1 (en) 2008-01-10
CN101484166B (zh) 2012-09-05
ES2443342T3 (es) 2014-02-19
UA106422C2 (uk) 2014-08-26
EA201401042A1 (ru) 2016-05-31
RS53461B (en) 2014-12-31
SI2359826T1 (sl) 2014-02-28
RS53084B (en) 2014-06-30
ME01648B (me) 2014-09-20
IL195433A0 (en) 2009-08-03
KR101433394B1 (ko) 2014-08-26
EA021461B1 (ru) 2015-06-30
NZ594369A (en) 2013-10-25
EP2359826B1 (en) 2013-10-30
ES2378281T3 (es) 2012-04-10
IL221309A (en) 2014-12-31
US20150272949A1 (en) 2015-10-01

Similar Documents

Publication Publication Date Title
CY1115462T1 (el) ΣΥΝΔΥΑΣΜΟΣ ΑΝΑΣΤΟΛΕΩΝ ΗΜG-CoΑ ΑΝΑΓΩΓΑΣΗΣ ΑΤΟΡΒΑΣΤΑΤΙΝΗΣ Ή ΣYΜΒΑΣΤΑΤΙΝΗΣ ΜΕ ΑΝΑΣΤΟΛΕΑ ΦΩΣΦΟΔΙΕΣΤΕΡΑΣΗΣ 4 ΟΠΩΣ ΡΟΦΛΟΥΜΙΛΑΣΤΗ ΓΙΑ ΤΗ ΘΕΡΑΠΕΙΑ ΦΛΕΓΜΟΝΩΔΩΝ ΠΝΕΥΜΟΝΙΚΩΝ ΑΣΘΕΝΕΙΩΝ
EA200702358A1 (ru) Комбинация ингибитора pde4 и производного тетрагидробиоптерина
SMP200900013B (it) Peptidomimetici smac utili come inibitori di iap
ECSP088972A (es) Isoindoles sustituidos como inhibidores de bace y su uso
ATE480543T1 (de) Tetrahydropyrrolopyrimidindione und ihre verwendung als inhibitoren der humanen neutrophilen elastase
GT200800123A (es) Compuestos mimeticos de lisina modificados
EP1933694A4 (en) EYE TRACKING DEVICE HAVING EXTENDED SCOPE OF OPERATING DISTANCES
EA200900798A1 (ru) Производные индол-4-илпиримидинил-2-иламина и их применение в качестве ингибиторов циклинзависимой киназы
CY1112477T1 (el) Φαρμακευτικο παρασκευασμα που εχει εξαιρετικh φωτοσταθεροτητα
EP1948168A4 (en) COMPOSITIONS AND TREATMENTS FOR INHIBITING KINASE AND / OR HMG-COA REDUCTASE
ATE524182T1 (de) 2,3-substituierte pyrazinsulfonamide als crth2- hemmer
BRPI0720050A2 (pt) 6-oxo-1,6-diidropirimidin-2-ilas no tratamento de doenças proliferativas
EA200801666A1 (ru) КОМБИНАЦИЯ ПРОИЗВОДНЫХ ТРИАЗИНА И ИНГИБИТОРОВ HMG-CoA РЕДУКТАЗЫ
DK1879862T3 (da) Magnesiumsalte af HMG-COA reduktaseinhibitorer
ECSP088374A (es) Formulacion de aerosol para inhalacion
EA200800342A1 (ru) ИНГИБИТОРЫ Glepp-1 ДЛЯ ЛЕЧЕНИЯ АУТОИММУННЫХ И/ИЛИ ВОСПАЛИТЕЛЬНЫХ РАССТРОЙСТВ
UA113806C2 (xx) Пероральний препарат для лікування серцево-судинних захворювань
WO2010076564A3 (en) Isochromenones useful in the treatment of inflammation
ES1059322Y (es) Conjunto de seguridad antirrobo de rodelas de compensacion de catenaria de ferrocarril
UY32953A (es) Nuevos derivados de piridazin-3(2h)-ona
ECSP078040A (es) Derivados de espiro