HRP20140073T1 - Kombinacija rosuvastatina inhibitora reduktaze hmg-coa s inhibitorom fosfodiesteraze-4, kao što je roflumilast, roflumilast-n-oksid, za lijeäśenje pluä†nih bolesti - Google Patents

Kombinacija rosuvastatina inhibitora reduktaze hmg-coa s inhibitorom fosfodiesteraze-4, kao što je roflumilast, roflumilast-n-oksid, za lijeäśenje pluä†nih bolesti Download PDF

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HRP20140073T1
HRP20140073T1 HRP20140073TT HRP20140073T HRP20140073T1 HR P20140073 T1 HRP20140073 T1 HR P20140073T1 HR P20140073T T HRP20140073T T HR P20140073TT HR P20140073 T HRP20140073 T HR P20140073T HR P20140073 T1 HRP20140073 T1 HR P20140073T1
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Croatia
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roflumilast
inhibitor
hmg
coa reductase
pharmaceutically acceptable
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HRP20140073TT
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Stefan-Lutz Wollin
Andrea Wohlsen
Clemens Braun
Degenhard Marx
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Takeda Gmbh
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Claims (34)

1. Farmaceutski sastav, naznačen time, da obuhvaća farmaceutsku formulaciju koja uključuje jednu količinu PDE4-inhibitora, jednu količinu inhibitora reduktaze HMG-CoA i barem jedno farmaceutski prihvatljivo pomoćno sredstvo, pri čemu je PDE4-inhibitor odabran iz skupine koju čine: ROFLUMILAST, farmaceutski prihvatljiva sol od ROFLUMILASTA, ROFLUMILAST-N-oksid i farmaceutski prihvatljiva sol od ROFLUMILAST-N-oksida, dok inhibitor reduktaze HMG-CoA je ROSUVASTATIN ili njegova farmaceutski prihvatljiva sol, te pritom prva količina i druga količina zajedno sastavljaju učinkovitu količinu za prevenciju ili liječenje upalne plućne bolesti.
2. Kombinirani proizvod, naznačen time, da sadrži sljedeće sastojke: (A) jednu količinu PDE4-inhibitora; (B) jednu količinu inhibitora reduktaze HMG-CoA; pri čemu prva količina i druga količina zajedno sastavljaju učinkovitu količinu za prevenciju ili liječenje upalne plućne bolesti, gdje svaki od sastojaka (A) i (B) je formuliran u mješavini s barem jednim farmaceutski prihvatljivim pomoćnim sredstvom, dok je PDE4-inhibitor odabran iz skupine koju čine: ROFLUMILAST, farmaceutski prihvatljiva sol od ROFLUMILASTA, ROFLUMILAST-N-oksid i farmaceutski prihvatljiva sol od ROFLUMILAST-N-oksida, a inhibitor reduktaze HMG-CoA je ROSUVASTATIN ili njegova farmaceutski prihvatljiva sol.
3. Garnitura, naznačena time, da sadrži sljedeće sastojke: (A) farmaceutska formulacija koja uključuje jednu količinu PDE4-inhibitora u mješavini s barem jednim farmaceutski prihvatljivim pomoćnim sredstvom; (B) farmaceutska formulacija koja uključuje jednu količinu inhibitora reduktaze HMG-CoA u mješavini s barem jednim farmaceutski prihvatljivim pomoćnim sredstvom; pri čemu prva količina i druga količina zajedno sastavljaju učinkovitu količinu za prevenciju ili liječenje upalne plućne bolesti, dok je PDE4-inhibitor odabran iz skupine koju čine: ROFLUMILAST, farmaceutski prihvatljiva sol od ROFLUMILASTA, ROFLUMILAST-N-oksid i farmaceutski prihvatljiva sol od ROFLUMILAST-N-oksida, a inhibitor reduktaze HMG-CoA je ROSUVASTATIN ili njegova farmaceutski prihvatljiva sol.
4. Farmaceutski sastav prema zahtjevu 1, naznačen time, da PDE4-inhibitor je ROFLUMILAST.
5. Farmaceutski sastav prema zahtjevu 1, naznačen time, da PDE4-inhibitor je ROFLUMILAST-N-oksid.
6. Farmaceutski sastav prema bilo kojem od zahtjeva 1, 4 ili 5, naznačen time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN hemi-kalcij.
7. Farmaceutski sastav prema bilo kojem od zahtjeva 1, 4 ili 5, naznačen time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN natrij.
8. Farmaceutski sastav prema bilo kojem od zahtjeva 1, 4 ili 5, naznačen time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN.
9. Kombinirani proizvod prema zahtjevu 2, naznačen time, da PDE4-inhibitor je ROFLUMILAST.
10. Kombinirani proizvod prema zahtjevu 2, naznačen time, da PDE4-inhibitor je ROFLUMILAST-N-oksid.
11. Kombinirani proizvod prema bilo kojem od zahtjeva 2, 9 ili 10, naznačen time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN hemi-kalcij.
12. Kombinirani proizvod prema bilo kojem od zahtjeva 2, 9 ili 10, naznačen time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN natrij.
13. Kombinirani proizvod prema bilo kojem od zahtjeva 2, 9 ili 10, naznačen time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN.
14. Garnitura prema zahtjevu 3, naznačena time, da PDE4-inhibitor je ROFLUMILAST.
15. Garnitura prema zahtjevu 3, naznačena time, da PDE4-inhibitor je ROFLUMILAST-N-oksid.
16. Garnitura prema bilo kojem od zahtjeva 3, 14 ili 15, naznačena time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN hemi-kalcij.
17. Garnitura prema bilo kojem od zahtjeva 3, 14 ili 15, naznačena time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN natrij.
18. Garnitura prema bilo kojem od zahtjeva 3, 14 ili 15, naznačena time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN.
19. Farmaceutski sastav prema bilo kojem od zahtjeva 1, 4, 5, 6, 7 ili 8, naznačen time, da je upalna plućna bolest odabrana iz skupine koju čine: astma, COPD, skleroza, alveolitis, sarkoidoza, idiopatska plućna fibroza i plućna hipertenzija.
20. Farmaceutski sastav prema bilo kojem od zahtjeva 1, 4, 5, 6, 7 ili 8, naznačen time, da upalna plućna bolest je COPD.
21. Kombinirani proizvod prema bilo kojem od zahtjeva 2, 9, 10, 11, 12 ili 13, naznačen time, da je upalna plućna bolest odabrana iz skupine koju čine: astma, COPD, skleroza, alveolitis, sarkoidoza, idiopatska plućna fibroza i plućna hipertenzija.
22. Kombinirani proizvod prema bilo kojem od zahtjeva 2, 9, 10, 11, 12 ili 13, naznačen time, da upalna plućna bolest je COPD.
23. Garnitura prema bilo kojem od zahtjeva 3, 14, 15, 16, 17 ili 18, naznačena time, da je upalna plućna bolest odabrana iz skupine koju čine: astma, COPD, skleroza, alveolitis, sarkoidoza, idiopatska plućna fibroza i plućna hipertenzija.
24. Garnitura prema bilo kojem od zahtjeva 3, 14, 15, 16, 17 ili 18, naznačena time, da upalna plućna bolest je COPD.
25. Uporaba PDE4-inhibitora i inhibitora reduktaze HMG-CoA, naznačena time, da je za proizvodnju lijeka, posebno farmacetskog sastava prema izumu, za prevenciju ili liječenje upalne plućne bolesti, pri čemu je PDE4-inhibitor odabran iz skupine koju čine: ROFLUMILAST, farmaceutski prihvatljiva sol od ROFLUMILASTA, ROFLUMILAST-N-oksid i farmaceutski prihvatljiva sol od ROFLUMILAST-N-oksida, a inhibitor reduktaze HMG-CoA je ROSUVASTATIN ili njegova farmaceutski prihvatljiva sol.
26. Uporaba PDE4-inhibitora i inhibitora reduktaze HMG-CoA, naznačena time, da je za proizvodnju dodatnog lijeka koji se daje uzastopno ili odvojeno uz prvi lijek, posebno kombiniranog proizvoda ili garniture prema izumu, za prevenciju ili liječenje upalne plućne bolesti, pri čemu je PDE4-inhibitor odabran iz skupine koju čine: ROFLUMILAST, farmaceutski prihvatljiva sol od ROFLUMILASTA, ROFLUMILAST-N-oksid i farmaceutski prihvatljiva sol od ROFLUMILAST-N-oksida, a inhibitor reduktaze HMG-CoA je ROSUVASTATIN ili njegova farmaceutski prihvatljiva sol.
27. Uporaba prema zahtjevu 25 ili 26, naznačena time, da PDE4-inhibitor je ROFLUMILAST.
28. Uporaba prema zahtjevu 25 ili 26, naznačena time, da PDE4-inhibitor je ROFLUMILAST-N-oksid.
29. Uporaba prema bilo kojem od zahtjeva 25, 26, 27 ili 28, naznačena time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN hemi-kalcij.
30. Uporaba prema bilo kojem od zahtjeva 25, 26, 27 ili 28, naznačena time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN natrij.
31. Uporaba prema bilo kojem od zahtjeva 25, 26, 27 ili 28, naznačena time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN.
32. Uporaba prema bilo kojem od zahtjeva 25 do 31, naznačena time, da je upalna plućna bolest odabrana iz skupine koju čine: astma, COPD, skleroza, alveolitis, sarkoidoza, idiopatska plućna fibroza i plućna hipertenzija.
33. Uporaba prema bilo kojem od zahtjeva 25 do 31, naznačena time, da upalna plućna bolest je COPD.
34. Postupak za proizvodnju farmaceutskog sastava prema bilo kojem od zahtjeva 1, 4, 5, 6, 7, 8, 19 ili 20, naznačen time, da obuhvaća miješanje PDE4-inhibitora ili njegove farmaceutski prihvatljive soli s inhibitorom reduktaze HMG-CoA ili s njegovom farmaceutski prihvatljivom soli.
HRP20140073TT 2006-07-05 2014-01-21 Kombinacija rosuvastatina inhibitora reduktaze hmg-coa s inhibitorom fosfodiesteraze-4, kao što je roflumilast, roflumilast-n-oksid, za lijeäśenje pluä†nih bolesti HRP20140073T1 (hr)

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HRP20140073TT HRP20140073T1 (hr) 2006-07-05 2014-01-21 Kombinacija rosuvastatina inhibitora reduktaze hmg-coa s inhibitorom fosfodiesteraze-4, kao što je roflumilast, roflumilast-n-oksid, za lijeäśenje pluä†nih bolesti
HRP20140707TT HRP20140707T1 (hr) 2006-07-05 2014-07-22 KOMBINACIJA ATORVASTATINA ILI SIMVASTATINA KAO INHIBITORA REDUKTAZE HMG-CoA S INHIBITOROM FOSFODIESTERAZE 4 KOJI JE ROFLUMILAST, ZA LIJEČENJE UPALNIH BOLESTI PLUĆA

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Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI436767B (zh) * 2008-03-14 2014-05-11 Otsuka Pharma Co Ltd 基質金屬蛋白酶-2(mmp-2)及/或基質金屬蛋白酶-9(mmp-9)抑制劑
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
CA2953209A1 (en) * 2014-06-05 2015-12-10 Transgenion-International Institute For Regenerative Translational Medicine Gmbh Methods of diagnosing chronic obstructive pulmonary disease (copd) using novel molecular biomarkers
JP6755242B2 (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
JP6755241B2 (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
US20210031012A1 (en) 2018-01-26 2021-02-04 Progenity, Inc. Treatment of a disease of the gastrointestinal tract with a pde4 inhibitor
WO2020106757A1 (en) 2018-11-19 2020-05-28 Progenity, Inc. Ingestible device for delivery of therapeutic agent to the gastrointestinal tract
US11707610B2 (en) 2019-12-13 2023-07-25 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
WO2024028388A1 (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
IL60219A (en) 1979-06-15 1985-05-31 Merck & Co Inc Hypocholesteremic fermentation products of the hmg-coa reductase inhibitor type,their preparation and pharmaceutical compositions containing them
AU548996B2 (en) 1980-02-04 1986-01-09 Merck & Co., Inc. Tetrahydro-2h-pyran-2-one derivatives
MX7065E (es) 1980-06-06 1987-04-10 Sankyo Co Un procedimiento microbiologico para preparar derivados de ml-236b
AU570021B2 (en) 1982-11-22 1988-03-03 Novartis Ag Analogs of mevalolactone
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
CA2396738C (en) 1990-11-30 2006-08-29 Masatoshi Chihiro Thiazole derivatives as active superoxide radical inhibitors
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
EP1380571A1 (en) * 1992-04-02 2004-01-14 Smithkline Beecham Corporation Compounds useful for treating allergic and inflammatory diseases
US5552438A (en) 1992-04-02 1996-09-03 Smithkline Beecham Corporation Compounds useful for treating allergic and inflammatory diseases
CZ290266B6 (cs) * 1993-07-02 2002-06-12 Byk Gulden Lomberg Chemische Fabrik Gmbh Substituované benzamidy, způsob jejich výroby a farmaceutické prostředky s jejich obsahem
GB9504460D0 (en) 1995-03-06 1995-04-26 Bayer Ag N-(3-Benzofuranyl)urea-derivatives
US6004974A (en) 1995-06-06 1999-12-21 Pfizer Inc Tricyclic 5,6-dihydro-9h-pyrazolo[3,4-c]-1,2,4-triazolo[4,3-α]pyridines
DE19636150A1 (de) 1996-09-06 1998-03-12 Asta Medica Ag N-substituierte Indol-3-glyoxylamide mit antiasthmatischer, antiallergischer und immunsuppressiver/immunmodulierender Wirkung
UA59443C2 (uk) 1998-04-28 2003-09-15 Арцнайміттельверк Дрезден Гмбх Гідроксііндол, спосіб його одержання, лікарська форма на його основі та спосіб її одержання
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
MY134008A (en) 1999-12-22 2007-11-30 Merck Frosst Canada Inc Subtituted 8-arylquinoline phospohodiestrase-4 inhibitors
US6410563B1 (en) * 1999-12-22 2002-06-25 Merck Frosst Canada & Co. Substituted 8-arylquinoline phosphodiesterase-4 inhibitors
JP2001294526A (ja) * 2000-02-10 2001-10-23 Takeda Chem Ind Ltd TNF−α抑制剤
AU2001232245A1 (en) 2000-02-10 2001-08-20 Takeda Chemical Industries Ltd. 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
CA2422820A1 (en) 2000-09-19 2002-03-28 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
EA200300836A1 (ru) * 2001-02-15 2004-02-26 Алтана Фарма Аг Производные фталазинон-пиперидина в качестве ингибиторов pde4
KR20100036390A (ko) * 2001-03-06 2010-04-07 셀러지 파마세우티칼스, 인크 비뇨생식기 장애 치료용 화합물 및 그 방법
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
AU2002257459B2 (en) * 2001-05-24 2006-12-14 Merck Frosst Canada Ltd 1-biaryl-1,8-napthyridin-4-one phosphodiesterase-4 inhibitors
CA2450686A1 (en) * 2001-06-27 2003-01-09 Merck Frosst Canada & Co./Merck Frosst Canada & Cie Substituted 8-arylquinoline pde4 inhibitors
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
EP1519922A1 (en) * 2002-07-02 2005-04-06 Merck Frosst Canada & Co. Di-aryl-substituted ethane pyridone pde4 inhibitors
BR0316256A (pt) * 2002-11-18 2005-10-04 Celgene Corp Métodos de inibir a produção de tnf-alfa e a atividade de pde4, de tratar ou prevenir uma doença ou um distúrbio, de controlar os nìveis de camp em uma célula e de produzir um composto, composição farmacêutica e composto
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
WO2004047829A1 (en) * 2002-11-27 2004-06-10 Altana Pharma Ag New synergistic combination comprising roflumilast and 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
US20040254238A1 (en) * 2003-04-07 2004-12-16 Osteoscreen Bone growth stimulation with NO/statin and other NO modulating combinations
DE602004020332D1 (de) 2003-04-11 2009-05-14 Glenmark Pharmaceuticals Sa Neue heterozyklische verbindungen, die sich für die behandlung von entzündlichen und allergischen erkrankungen eignen: verfahren zu deren herstellung und pharmazeutische zusammensetzungen, die diese enthalten
CN100441185C (zh) * 2003-04-30 2008-12-10 麦克弗罗斯特加拿大有限公司 8-(3-联芳基)苯基喹啉磷酸二酯酶-4抑制剂
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
WO2004103407A2 (en) * 2003-05-22 2004-12-02 Altana Pharma Ag Composition comprising a pde4 inhibitor and a pde5 inhibitor
WO2004110368A2 (en) * 2003-06-06 2004-12-23 Merck & Co., Inc. 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
CA2563693C (en) * 2004-04-19 2010-07-06 Loma Linda University Composition and method of decreasing renal ischemic damage
ZA200609228B (en) * 2004-04-23 2008-05-28 Celgene Corp 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
EP1894576B1 (en) 2005-06-08 2011-05-25 Kowa Company, Ltd. Novel triglyceride reducing agent
AU2006304787A1 (en) 2005-10-21 2007-04-26 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
AU2006313430B2 (en) 2005-11-08 2012-09-06 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

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