RU97121002A - USE OF R-ENANTIOMER OF N-PROPARGYL-1-AMINOINDANE, ITS SALTS AND COMPOSITIONS CONTAINING THEM - Google Patents

USE OF R-ENANTIOMER OF N-PROPARGYL-1-AMINOINDANE, ITS SALTS AND COMPOSITIONS CONTAINING THEM

Info

Publication number
RU97121002A
RU97121002A RU97121002/14A RU97121002A RU97121002A RU 97121002 A RU97121002 A RU 97121002A RU 97121002/14 A RU97121002/14 A RU 97121002/14A RU 97121002 A RU97121002 A RU 97121002A RU 97121002 A RU97121002 A RU 97121002A
Authority
RU
Russia
Prior art keywords
propargyl
use according
pharmaceutically acceptable
acceptable salt
salt
Prior art date
Application number
RU97121002/14A
Other languages
Russian (ru)
Other versions
RU2203653C2 (en
Inventor
Б.Х.Юдим Мусса
П.М.Финберг Джон
Леви Рут
Стерлинг Джеффри
Лернер Дэвид
Йеллин Хаим
Вайнберг Алекс
Original Assignee
Тева Фармасьютикал Индастриз Лтд.
Текнион Рисерч Энд Дивелопмент Фаундейшн Лтд.
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
Priority claimed from US08/446,439 external-priority patent/US5744500A/en
Application filed by Тева Фармасьютикал Индастриз Лтд., Текнион Рисерч Энд Дивелопмент Фаундейшн Лтд. filed Critical Тева Фармасьютикал Индастриз Лтд.
Publication of RU97121002A publication Critical patent/RU97121002A/en
Application granted granted Critical
Publication of RU2203653C2 publication Critical patent/RU2203653C2/en

Links

Claims (9)

1. Использование R(+)-N-пропаргил-1-аминоиндана или его фармацевтически приемлемой соли для получения фармацевтической композиции для лечения ишемии мозга, удара, поражения при травме головы, поражение при травме позвоночника, нейротравмы, нейродегенеративного заболевания или нейротоксического поражения; или для предотвращения нервного поражения у субъекта.1. The use of R (+) - N-propargyl-1-aminoindan or its pharmaceutically acceptable salt for the preparation of a pharmaceutical composition for the treatment of cerebral ischemia, stroke, damage to a head injury, damage to a spinal injury, neurotrauma, neurodegenerative disease or neurotoxic lesion; or to prevent nerve damage in a subject. 2. Использование по п.1, где при лечении ишемии мозга или удара область ишемического поражения мозга уменьшается на 35%. 2. The use according to claim 1, where in the treatment of cerebral ischemia or stroke, the area of ischemic brain damage is reduced by 35%. 3. Использование по п.1, где нервное нарушение представляют собой нарушение структуры нерва или нарушение структуры зрительного нерва. 3. The use according to claim 1, where the nervous disorder is a violation of the structure of the nerve or a violation of the structure of the optic nerve. 4. Использование по любому из пп.1-3, где фармацевтически приемлемую соль R(+)-N-пропаргил-1-аминоиндана выбирают из группы, состоящей из: мезилатной соли; этилсульфонатной соли; сульфатной соли и гидрохлоридной соли. 4. The use according to any one of claims 1 to 3, wherein the pharmaceutically acceptable salt of R (+) - N-propargyl-1-aminoindan is selected from the group consisting of: a mesylate salt; ethyl sulfonate salt; sulfate salt and hydrochloride salt. 5. Использование по любому из пп.1-4, где эффективное количество R(+)-N-пропаргил-1-аминоиндана или его фармацевтически приемлемой соли, которое должно быть введено, составляет 0,5 - 2,5 мг/кг веса тела субъекта. 5. The use according to any one of claims 1 to 4, where the effective amount of R (+) - N-propargyl-1-aminoindane or its pharmaceutically acceptable salt to be administered is 0.5 to 2.5 mg / kg body of the subject. 6. Использование по любому из пп.1-5, где R(+)-N-пропаргил-1-аминоиндан или его фармацевтически приемлемую соль вводят внутривенно, перорально, ректально, трансдермально или парентерально. 6. The use according to any one of claims 1 to 5, wherein R (+) - N-propargyl-1-aminoindane or a pharmaceutically acceptable salt thereof is administered intravenously, orally, rectally, transdermally or parenterally. 7. Использование по любому из пп.1-4, где субъектом является человек и эффективное количество составляет 0,01 - 50,0 мг в сутки. 7. The use according to any one of claims 1 to 4, where the subject is a person and an effective amount is 0.01 to 50.0 mg per day. 8. Использование по п. 7, где эффективное количество составляет 0,1 - 10,0 мг в сутки. 8. The use of claim 7, wherein the effective amount is 0.1 to 10.0 mg per day. 9. Использование по п. 7 или 8, где R(+)-N-пропаргил-1-аминоиндан или его фармацевтически приемлемую соль вводят внутривенно. 9. The use of claim 7 or 8, wherein R (+) - N-propargyl-1-aminoindan or a pharmaceutically acceptable salt thereof is administered intravenously.
RU97121002/14A 1995-05-22 1996-05-22 Using n-propargyl-1-aminoindane r-enantiomer, its salts and compositions comprising thereof RU2203653C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US08/446,439 US5744500A (en) 1990-01-03 1995-05-22 Use of R-enantiomer of N-propargyl-1-aminoindan, salts, and compositions thereof
US08/446,439 1995-05-22

Publications (2)

Publication Number Publication Date
RU97121002A true RU97121002A (en) 1999-09-27
RU2203653C2 RU2203653C2 (en) 2003-05-10

Family

ID=23772591

Family Applications (1)

Application Number Title Priority Date Filing Date
RU97121002/14A RU2203653C2 (en) 1995-05-22 1996-05-22 Using n-propargyl-1-aminoindane r-enantiomer, its salts and compositions comprising thereof

Country Status (22)

Country Link
US (6) US5744500A (en)
EP (1) EP0828485A4 (en)
JP (1) JP3341898B2 (en)
KR (1) KR100412154B1 (en)
CN (1) CN1096853C (en)
AU (1) AU699090B2 (en)
BR (1) BR9608733A (en)
CA (1) CA2221458A1 (en)
CZ (1) CZ288724B6 (en)
EE (1) EE03741B1 (en)
HK (1) HK1015269A1 (en)
HU (1) HUP9901629A3 (en)
IL (1) IL118247A (en)
LT (1) LT4455B (en)
LV (1) LV12083B (en)
MX (1) MX9708977A (en)
NO (1) NO975331L (en)
NZ (1) NZ308866A (en)
PL (1) PL184124B1 (en)
RU (1) RU2203653C2 (en)
SK (1) SK283675B6 (en)
WO (1) WO1996037199A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2622999C2 (en) * 2011-03-14 2017-06-21 Н.В. Нютрисиа Method for neurotrauma treatment

Families Citing this family (82)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5744500A (en) 1990-01-03 1998-04-28 Teva Pharmaceutical Industries, Ltd. Use of R-enantiomer of N-propargyl-1-aminoindan, salts, and compositions thereof
US5877218A (en) * 1994-01-10 1999-03-02 Teva Pharmaceutical Industries, Ltd. Compositions containing and methods of using 1-aminoindan and derivatives thereof and process for preparing optically active 1-aminoindan derivatives
US5726969A (en) * 1994-12-28 1998-03-10 Matsushita Electric Industrial Co., Ltd. Optical recording medium having dual information surfaces
IL118836A (en) * 1996-07-11 2001-01-11 Teva Pharma Pharmaceutical compositions comprising s-(-)-n-propargyl-1-aminoindan
US7129061B1 (en) * 1996-08-07 2006-10-31 Biogen Idec Ma Inc. Tumor necrosis factor related ligand
GB9715082D0 (en) * 1997-07-17 1997-09-24 Scherer Ltd R P Treatment of attention deficit hyperactivity disorder and narcolepsy
US6232326B1 (en) 1998-07-14 2001-05-15 Jodi A. Nelson Treatment for schizophrenia and other dopamine system dysfunctions
DE60029131T2 (en) 1999-10-27 2007-01-18 Teva Pharmaceutical Industries Ltd. USE OF 1-AMINOINDANE DERIVATIVES FOR THE TREATMENT OF MANIE IN CONNECTION WITH MANIC-DEPRESSIVE DISEASE
DE60231896D1 (en) 2001-11-05 2009-05-20 Krele Pharmaceuticals Llc COMPOSITIONS AND METHODS FOR INCREASING THE COMPLIANCE WITH THERAPIES USING ALDEHYDEDEHYDROGENASE INHIBITORS AND TREATING ALCOHOL MUSIC
US20040010038A1 (en) * 2002-02-27 2004-01-15 Eran Blaugrund Propargylamino indan derivatives and propargylamino tetralin derivatives as brain-selective MAO inhibitors
US8058442B2 (en) * 2002-11-07 2011-11-15 Technion Research And Development Foundation Ltd. Neuroprotective iron chelators and pharmaceutical compositions comprising them
EP1567152B1 (en) * 2002-11-15 2013-08-14 Teva Pharmaceutical Industries Limited Use of rasagiline with riluzole to treat amyotrophic lateral sclerosis
US20040176430A1 (en) * 2002-11-21 2004-09-09 Jeffrey Sterling Propargyl-trifluoromethoxy-amino-benzothiazole derivatives
CN1605336A (en) 2003-10-10 2005-04-13 中国医学科学院药物研究所 Application of L-butylphthalide in the process for preparing cerebral infarction preventing and treating medicine
CA2547053C (en) * 2003-11-25 2014-05-27 Technion Research & Development Foundation Ltd. Compositions and methods for treatment of cardiovascular disorders and diseases
US8097608B2 (en) * 2003-11-25 2012-01-17 Technion Research And Development Foundation Ltd. Methods for treatment of cardiovascular disorders and diseases
JP2005232148A (en) * 2004-02-03 2005-09-02 Technion Research & Development Foundation Ltd Use of propargylamine as neuroprotective agent
US20050197365A1 (en) * 2004-02-27 2005-09-08 Jeffrey Sterling Diamino thiazoloindan derivatives and their use
US20060018957A1 (en) * 2004-07-26 2006-01-26 Lerner E I Pharmaceutical dosage forms including rasagiline
US20060025446A1 (en) * 2004-07-27 2006-02-02 Jeffrey Sterling Propargyl nitroxides and indanyl nitroxides and their use for the treatment of neurologic diseases and disorders
WO2006014968A2 (en) * 2004-07-27 2006-02-09 Teva Pharmaceutical Industries, Ltd. Propargyl nitroxydes and indanyl nitroxides and their use for the treatment of neurologic diseases and disorders
US20080261894A1 (en) * 2005-02-17 2008-10-23 Rivka Kreitman Combination Therapy with Glatiramer Acetate and Rasagiline for the Treatment of Multiple Sclerosis
US20100167983A1 (en) * 2007-10-22 2010-07-01 Teva Pharmaceutical Industries, Ltd. Combination therapy with glatiramer acetate and rasagiline for the treatment of multiple sclerosis
EP2332408B1 (en) 2005-02-17 2013-11-13 Biogen Idec MA Inc. Treating neurological disorders
KR20140103356A (en) * 2005-02-23 2014-08-26 테바 파마슈티컬 인더스트리즈 리미티드 Rasagiline formulations of improved content uniformity
US8022104B2 (en) * 2005-02-24 2011-09-20 Yissum Research Development Company Of The Hebrew University Of Jerusalem Formulations of ladostigil tartrate
JP5339901B2 (en) 2005-05-10 2013-11-13 バイオジェン・アイデック・エムエイ・インコーポレイテッド Treatment and evaluation of inflammatory injury
WO2006130726A2 (en) * 2005-06-01 2006-12-07 Teva Pharmaceutical Industries, Ltd. Use of ladostigil for the treatment of multiple sclerosis
FR2886549B1 (en) * 2005-06-06 2007-09-07 Biocodex PHARMACEUTICAL COMPOSITION FOR PREVENTING OR TREATING CEREBRAL EDEMA
US8263655B2 (en) * 2005-10-06 2012-09-11 Technion Research And Development Foundation Ltd Methods for treatment of renal failure
US7491847B2 (en) * 2005-11-17 2009-02-17 Teva Pharmaceutical Industries, Ltd. Methods for isolating propargylated aminoindans
US7572834B1 (en) 2005-12-06 2009-08-11 Teva Pharmaceutical Industries, Ltd. Rasagiline formulations and processes for their preparation
JP2009518433A (en) * 2005-12-09 2009-05-07 イッサム リサーチ ディベロップメント カンパニー オブ ザ ヘブライ ユニバーシティー オブ エルサレム Use of low-dose radostigil for neuroprotection
US20070135518A1 (en) * 2005-12-09 2007-06-14 Marta Weinstock-Rosin Use of low-dose ladostigil for neuroprotection
US20110047685A1 (en) * 2006-02-16 2011-03-03 Ferrara Vincent R Impact energy management method and system
JP5701485B2 (en) 2006-02-21 2015-04-15 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 Use of rasagiline for the treatment of multiple system atrophy
TW200744576A (en) * 2006-02-24 2007-12-16 Teva Pharma Propargylated aminoindans, processes for preparation, and uses thereof
WO2007117431A2 (en) * 2006-04-03 2007-10-18 Teva Pharmaceutical Industries, Ltd. Use of rasagiline for the treatment of restless legs syndrome
CN101062897B (en) * 2006-04-25 2011-11-23 重庆医药工业研究院有限责任公司 Improved process for preparing 2,3-dihydro-1H-indenes-1-amine and derivative thereof
EP1892233A1 (en) * 2006-08-18 2008-02-27 Ratiopharm GmbH New salts of the active component rasagiline
PT2101569E (en) * 2006-12-14 2012-01-13 Teva Pharma Crystalline solid rasagiline base
DK2101570T3 (en) 2006-12-14 2013-05-27 Teva Pharma Tannate salt of rasagiline
EP1987816A1 (en) * 2007-04-30 2008-11-05 Ratiopharm GmbH Adsorbate of a rasagiline salt with a water-soluble inactive ingredient
JP2010538067A (en) * 2007-09-05 2010-12-09 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 Treatment of glaucoma using rasagiline
US8188149B2 (en) * 2007-09-17 2012-05-29 Teva Pharmaceutical Industries, Ltd. Use of R(+)-N-propargy1-1-aminoindan to treat or prevent hearing loss
US20090181086A1 (en) * 2008-01-11 2009-07-16 Muhammad Safadi Rasagiline formulations, their preparation and use
WO2009118657A2 (en) * 2008-03-28 2009-10-01 Medichem, S.A. Polymorphic form of an aminoindan mesylate derivative
WO2009147432A1 (en) * 2008-06-02 2009-12-10 Generics [Uk] Limited An improved process for the preparation of amines
CA2723869C (en) * 2008-06-02 2013-07-16 Generics [Uk] Limited A process for the preparation of enantiomerically pure amines
ES2389353T3 (en) * 2008-06-10 2012-10-25 Teva Pharmaceutical Industries Ltd. Rasagiline soft gelatin capsules
WO2009151625A1 (en) * 2008-06-13 2009-12-17 Teva Pharmaceutical Industries, Ltd. Rasagiline for parkinson's disease modification
CA2727017A1 (en) * 2008-06-19 2009-12-23 Teva Pharmaceutical Industries Ltd. Process for preparing and drying solid rasagiline base
EP2299993A4 (en) * 2008-06-19 2014-08-20 Teva Pharma Process for purifying rasagiline base
WO2011012140A2 (en) 2008-07-11 2011-02-03 Synthon Bv Polymorphs of rasagiline hydrochloride
EP2321258A1 (en) * 2008-07-30 2011-05-18 Generics [UK] Limited Polymorphic form of rasagiline mesylate
EP2218444A3 (en) 2009-01-23 2010-08-25 Teva Pharmaceutical Industries, Ltd. Delayed release rasagiline formulation
US20100189791A1 (en) * 2009-01-23 2010-07-29 Teva Pharmaceutical Industries, Ltd. Delayed release rasagiline malate formulation
CN102365265A (en) * 2009-04-09 2012-02-29 欧加农股份有限公司 Indane derivatives
EP2451771B1 (en) 2009-07-09 2014-06-18 Ratiopharm GmbH Salts of rasagiline and pharmaceutical preparations thereof
CN102048717B (en) 2009-10-29 2014-02-19 重庆医药工业研究院有限责任公司 Stable rasagiline composition
EP2325159A1 (en) 2009-11-24 2011-05-25 LEK Pharmaceuticals d.d. Novel salts of rasagiline
US8741962B2 (en) * 2009-11-26 2014-06-03 Usv Limited Process for preparation of Rasagiline and salts thereof
EP2939669A1 (en) 2009-12-22 2015-11-04 Teva Pharmaceutical Industries, Ltd. 3-keto-n-propargyl-1-aminoindan
RU2734632C2 (en) 2010-02-03 2020-10-21 Фарма Ту Б Лтд. Rasagiline compositions with prolonged release and use thereof
EP2563347B1 (en) 2010-04-30 2016-10-12 Teikoku Pharma USA, Inc. Propynylaminoindan transdermal compositions
CA2806737A1 (en) 2010-07-27 2012-02-02 Teva Pharmaceutical Industries Ltd. Dispersions of rasagiline citrate
US8569379B2 (en) 2010-07-27 2013-10-29 Teva Pharmaceutical Industries Ltd. Use of rasagiline for the treatment of olfactory dysfunction
DK2611440T3 (en) 2010-09-01 2017-05-15 Tonix Pharmaceuticals Inc Treatment for cocaine addiction
AU2011320611A1 (en) 2010-10-26 2013-06-13 Teva Pharmaceutical Industries Ltd. Deuterium enriched rasagiline
WO2012129429A2 (en) 2011-03-24 2012-09-27 Teikoku Pharma Usa, Inc. Transdermal compositions comprising an active agent layer and an active agent conversion layer
EP2766004A4 (en) 2011-10-10 2015-04-22 Teva Pharma R(+)-n-methyl-propargyl-aminoindan
US9346746B2 (en) 2011-10-10 2016-05-24 Teva Pharmaceutical Industries, Ltd. R(+)-N-formyl-propargyl-aminoindan
US9913812B2 (en) 2011-11-09 2018-03-13 Teikoku Pharma Usa, Inc. Methods for the treatment of skin neoplasms
MX343986B (en) 2012-03-21 2016-12-01 Synthon Bv Stabilized pharmaceutical compositions comprising rasagiline salts.
WO2013175493A1 (en) 2012-04-09 2013-11-28 Cadila Healthcare Limited Stable oral pharmaceutical compositions
AR092168A1 (en) 2012-08-17 2015-03-25 Teva Pharma PARENTERAL FORMULATIONS OF RASAGILINA
US10918607B2 (en) 2012-11-02 2021-02-16 Teikoku Pharma Usa, Inc. Propynylaminoindan transdermal compositions
EP2796130A3 (en) * 2013-02-06 2015-02-25 Galenicum Health S.L. Immediate release tablets of rasagiline hemitartrate
ES2502140T1 (en) * 2013-02-06 2014-10-02 Galenicum Health S.L. Rasagiline hemitartrate immediate-release tablets
WO2014141280A1 (en) * 2013-03-13 2014-09-18 Abital Pharma Pipelines Ltd. Methods, compositions and devices for treatment of motor and depression symptoms associated with parkinson's disease
CN103804200B (en) * 2014-02-21 2015-04-29 常州市第四制药厂有限公司 Preparation method of rasagiline and analogue thereof
US11701340B2 (en) * 2019-04-17 2023-07-18 Vici Health Sciences., Llc Liquid pharmaceutical compositions

Family Cites Families (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US513244A (en) * 1894-01-23 Island
US3201470A (en) * 1965-08-17 Chsx c cech
US3253037A (en) * 1962-06-19 1966-05-24 Ciba Geigy Corp N-2-alkynyl-amino-benzocylo-alkanes
GB1187017A (en) 1966-07-16 1970-04-08 Aspro Nicholas Ltd Substituted 1-Amino Indanes and Tetrahydronaphthalens
GB1037014A (en) 1963-08-02 1966-07-20 Aspro Nicholas Ltd Derivatives of 1-aminoindane
US3513249A (en) * 1968-12-24 1970-05-19 Ideal Ind Explosion connector with improved insulating means
GB1548022A (en) 1976-10-06 1979-07-04 Wyeth John & Brother Ltd Pharmaceutial dosage forms
DE3779500T2 (en) 1986-06-10 1993-01-21 Chiesi Farma Spa LEVODOPA METHYL ESTER CONTAINING PHARMACEUTICAL COMPOSITIONS, THEIR PRODUCTION AND THERAPEUTIC USE.
ES2052593T3 (en) 1986-08-21 1994-07-16 Roussel Uclaf PROCEDURE FOR PREPARING DERIVATIVES OF INDANO.
HU197510B (en) 1986-12-19 1989-04-28 Chinoin Gyogyszer Es Vegyeszet Process for producing pharmaceutical composition containing phenyl-alkyl-amine derivatives, against motion-sick
US4855326A (en) * 1987-04-20 1989-08-08 Fuisz Pharmaceutical Ltd. Rapidly dissoluble medicinal dosage unit and method of manufacture
CA1327795C (en) 1987-08-14 1994-03-15 Jules Freedman Antidepressants which are aryloxy inadanamines
FR2626877B1 (en) 1988-02-05 1991-04-05 Delalande Sa ALKYLIC OR BENZYL ETHERS OF PHENOL, PROCESSES FOR THEIR PREPARATION AND THEIR APPLICATION IN THERAPEUTICS
HU208484B (en) 1988-08-17 1993-11-29 Chinoin Gyogyszer Es Vegyeszet Process for producing pharmaceutical composition containing acid additional salt of selegilin as active component for treating schisofrenia
GB8909793D0 (en) 1989-04-28 1989-06-14 Beecham Group Plc Pharmaceutical formulation
US5079018A (en) * 1989-08-14 1992-01-07 Neophore Technologies, Inc. Freeze dry composition and method for oral administration of drugs, biologicals, nutrients and foodstuffs
JPH04504760A (en) 1989-09-25 1992-08-20 アメリカ合衆国 Evaluation methods for detecting inflammatory responses and predicting responses to stress
DK0494972T3 (en) 1989-10-02 1997-05-12 Cima Labs Inc Shower dose form and method of administration thereof
FR2655044B1 (en) 1989-11-24 1995-03-03 Delalande Sa DERIVATIVES OF (HETERO) ARYLMETHYLOXY-4 PHENYL TETRAZOLE AND OXADIAZOLE, THEIR PREPARATION PROCESS AND THEIR THERAPEUTIC APPLICATION.
JPH03176457A (en) 1989-12-04 1991-07-31 Nippon Paint Co Ltd Novel propargyl compound, its production and coating material containing the same compound
IL92952A (en) 1990-01-03 1994-06-24 Teva Pharma R-enantiomers of n-propargyl-1-aminoindan compounds, their preparation and pharmaceutical compositions containing them
US5744500A (en) * 1990-01-03 1998-04-28 Teva Pharmaceutical Industries, Ltd. Use of R-enantiomer of N-propargyl-1-aminoindan, salts, and compositions thereof
CA2039742A1 (en) 1990-04-23 1991-10-24 Andrew B. Dennis Tablet composition and method for problem pharmaceutical materials
US5169868A (en) 1991-03-01 1992-12-08 University Of Saskatchewan Aliphatic propargylamines as specific mao-b inhibitors
US5767164A (en) * 1991-04-04 1998-06-16 Innovations Foundation Use of deprenyl to rescue damaged nerve cells
US5444095A (en) * 1991-04-04 1995-08-22 University Of Toronto, Innovations Foundation Use of deprenyl to rescue damaged nerve cells
US5844003A (en) * 1991-04-04 1998-12-01 Innovations Foundation Use of deprenyl compounds to maintain, prevent loss, or recover nerve cell function
IL112819A (en) 1991-10-16 2001-11-25 Teva Pharma Fluorinated 1-aminoindan compounds and a process for their preparation
WO1993012769A1 (en) 1991-12-24 1993-07-08 Yamanouchi Pharmaceutical Co., Ltd. Intrabuccally disintegrating preparation and production thereof
US5298261A (en) * 1992-04-20 1994-03-29 Oregon Freeze Dry, Inc. Rapidly distintegrating tablet
WO1993025197A1 (en) 1992-06-12 1993-12-23 Affymax Technologies N.V. Compositions and methods for enhanced drug delivery
SE501848C2 (en) 1992-11-18 1995-06-06 Kvaerner Pulping Tech Method to cook pulp continuously at constant temperature
IL111240A (en) 1993-10-18 2001-10-31 Teva Pharma Salts of r(+) - enantiomers of n- propargyl-1-aminoindan and pharmaceutical compositions comprising them
IL112779A (en) 1994-03-01 1999-11-30 Gergely Gerhard Granular product or tablet containing an efferescent system and an active pharmaceutical substance and its preparation
NZ302723A (en) 1995-03-02 1998-04-27 Scherer Ltd R P Composition comprising monoamine oxidase b inhibitor and a carrier formulated for pre-gastric absorption of the monoamine oxidase b inhibitor
IL115357A (en) 1995-09-20 2000-01-31 Teva Pharma Stable compositions containing N-propargyl-1-aminoindan and polyhydric alcohols
IL118836A (en) 1996-07-11 2001-01-11 Teva Pharma Pharmaceutical compositions comprising s-(-)-n-propargyl-1-aminoindan
WO1999037293A2 (en) * 1998-01-27 1999-07-29 Thomas Thomas N Use of an mao-a or mao-b inhibitor for the treatment of vascular disorders
FI104042B1 (en) * 1998-09-29 1999-11-15 Aaro Kiuru Method for measuring pulmonary perfusion
US6248363B1 (en) * 1999-11-23 2001-06-19 Lipocine, Inc. Solid carriers for improved delivery of active ingredients in pharmaceutical compositions
US20030180352A1 (en) * 1999-11-23 2003-09-25 Patel Mahesh V. Solid carriers for improved delivery of active ingredients in pharmaceutical compositions
CA2452738C (en) * 2001-07-04 2011-06-14 Sun Pharmaceutical Industries Limited Gastric retention controlled drug delivery system
US20040010038A1 (en) * 2002-02-27 2004-01-15 Eran Blaugrund Propargylamino indan derivatives and propargylamino tetralin derivatives as brain-selective MAO inhibitors
US20040166159A1 (en) * 2002-05-29 2004-08-26 Chien-Hsuan Han Pharmaceutical dosage forms having immediate and controlled release properties that contain an aromatic amino acid decarboxylase inhibitor and levodopa
US20060009483A1 (en) * 2002-05-31 2006-01-12 Bayer Pharmaceuticals Corporation Compounds and compositions for the treatment of diabetes and diabetes-related disorders
US20040115254A1 (en) * 2002-09-06 2004-06-17 Genteric, Inc. Microcapsules and methods of use
EP1567152B1 (en) * 2002-11-15 2013-08-14 Teva Pharmaceutical Industries Limited Use of rasagiline with riluzole to treat amyotrophic lateral sclerosis
US20050026979A1 (en) * 2003-07-31 2005-02-03 Maha Ghazzi Methods for treating inflammation and inflammation-associated diseases with a statin and ether
KR20140103356A (en) * 2005-02-23 2014-08-26 테바 파마슈티컬 인더스트리즈 리미티드 Rasagiline formulations of improved content uniformity

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2622999C2 (en) * 2011-03-14 2017-06-21 Н.В. Нютрисиа Method for neurotrauma treatment

Similar Documents

Publication Publication Date Title
RU97121002A (en) USE OF R-ENANTIOMER OF N-PROPARGYL-1-AMINOINDANE, ITS SALTS AND COMPOSITIONS CONTAINING THEM
KR890701559A (en) 3-indolepyruvic acid derivatives and pharmaceutical uses thereof
RU2203653C2 (en) Using n-propargyl-1-aminoindane r-enantiomer, its salts and compositions comprising thereof
CA2260037A1 (en) Pharmaceutical compositions comprising s-(-)-n-propargyl-1-aminoindan
SI9111227B (en) Pharmaceutical composition with an active agent Flupirtine for treating muscle tension
RU95114405A (en) USE OF RILUZOL AS A MEDICINAL PRODUCT FOR TREATMENT OF NEUROLOGICAL DISORDERS CAUSED BY INJURIES AND METHOD FOR PRODUCING A MEDICINE
HUP9900508A2 (en) Use of 4-amino-4-(4-fluorobenzylamino)-1-ethoxy-carbonylaminobenzene for prophylaxis and treatment of sequelae of reduced circulation in the brain and neurodegenerative disorders
US4497826A (en) Antiparkinsonian agent
RU97114608A (en) METHOD FOR TREATING CEREBRAL ISCHEMIA AND CEREBRAL DAMAGE TO NEUROPROTECTIVE MEANS
CA2492081A1 (en) Pharmaceutical compositions comprising dextromethorphan and quinidine for the treatment of neurological disorders
EP1621195A3 (en) The use of pyridinic NK-1 receptor antagonists for the treatment of brain, spinal or nerve injury
DE102008037682A1 (en) Use of equipotent doses of local anesthetics or derivatives thereof for the treatment of chronic pain
NO306509B1 (en) Pyrimidine derivatives, their use and pharmaceutical preparation
CA2459470A1 (en) Pharmaceutical composition comprising gabapentin or an analogue thereof and an .alpha.-aminoamide and its analgesic use
CA2143610A1 (en) Use of norastemizole for the treatment of allergic disorders
RU94034109A (en) AGENT FOR THE TREATMENT OF THE STATE OF ALARM
GB2259013A (en) Neuroprotective use of CCK antagonists
JP2717844B2 (en) Novel therapeutic pharmaceutical composition
JP2000204049A (en) Therapy and control of development of eye
DE69814089T2 (en) USE OF A DRAFLAZINE ANALOGUE FOR TREATMENT
US3995058A (en) Treatment of ethanol withdrawal symptoms with levodopa
DE60125062T2 (en) Quetiapine for the treatment of dyskinesia in non-psychotic patients
JPH02502920A (en) Pharmaceutical composition for the treatment of epileptic seizures
WO1997044045A1 (en) Malatonin in combination with analgesics
KR100757226B1 (en) A pharmaceutical composition comprising adatanserin for the treatment of neurodegenerative conditions