AR062659A1 - Composicion de liberacion sostenida de levodopa y metodo para su uso - Google Patents

Composicion de liberacion sostenida de levodopa y metodo para su uso

Info

Publication number
AR062659A1
AR062659A1 ARP070103916A ARP070103916A AR062659A1 AR 062659 A1 AR062659 A1 AR 062659A1 AR P070103916 A ARP070103916 A AR P070103916A AR P070103916 A ARP070103916 A AR P070103916A AR 062659 A1 AR062659 A1 AR 062659A1
Authority
AR
Argentina
Prior art keywords
levodopa
subject
composition
interval
hours
Prior art date
Application number
ARP070103916A
Other languages
English (en)
Inventor
Michael Grimshaw
Jonathan Bortz
Michael F Dickus
David F Erkoboni
Original Assignee
Drug Tech Corp
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 Drug Tech Corp filed Critical Drug Tech Corp
Publication of AR062659A1 publication Critical patent/AR062659A1/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/197Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
    • A61K31/198Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0053Mouth and digestive tract, i.e. intraoral and peroral administration
    • A61K9/0065Forms with gastric retention, e.g. floating on gastric juice, adhering to gastric mucosa, expanding to prevent passage through the pylorus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/205Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/205Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose

Landscapes

  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical & Material Sciences (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Physiology (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Nutrition Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Psychology (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicinal Preparation (AREA)

Abstract

Composiciones farmacéuticas que comprende levodopa y que, cuando se administra en una dosis unitaria de levodopa de alrededor de 100 hasta alrededor de 500 mg con un intervalo entre tomas de alrededor de 6 hasta alrededor de 24 horas, exhibe un período de liberacion suficientemente prolongado y un tiempo de residencia suficientemente prolongado en el tracto gastrointestinal alto para proporcional una concentracion mínima de levodopa en el plasma del sujeto que no es inferior a una concentracion umbral mínima por debajo de la cual se observan en el sujeto efectos motores adversos. También se proporciona un método para tratar la enfermedad de Parkinson en un sujeto, que comprende administrar por vía oral dicha composicion al sujeto en una dosis unitaria de levodopa de alrededor de 50 hasta alrededor de 1000 mg con un intervalo entre tomas de alrededor de 3 hasta alrededor de 24 horas. Reivindicacion 1: Una composicion farmacéutica que se puede administrar por vía oral y que comprende levodopa y al menos un excipiente adecuado para uso farmacéutico, caracterizada porque la composicion, cuando se administra por vía oral en una dosis unitaria de levodopa de alrededor de 100 hasta alrededor de 50 mg a un sujeto humano con un intervalo entre tomas de alrededor de 6 hasta alrededor de 24 horas, exhibe (a) un período de liberacion de levodopa suficientemente prolongado y (b) un tiempo de resistencia en el tracto gastrointestinal alto del sujeto suficientemente prolongado para proporcionar una concentracion mínima de levodopa en el plasma del sujeto que no es inferior a una concentracion umbral mínima de alrededor de 300 ng/ml.
ARP070103916A 2006-09-08 2007-09-05 Composicion de liberacion sostenida de levodopa y metodo para su uso AR062659A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US82498506P 2006-09-08 2006-09-08
US82827606P 2006-10-05 2006-10-05

Publications (1)

Publication Number Publication Date
AR062659A1 true AR062659A1 (es) 2008-11-26

Family

ID=39157983

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP070103916A AR062659A1 (es) 2006-09-08 2007-09-05 Composicion de liberacion sostenida de levodopa y metodo para su uso

Country Status (5)

Country Link
US (1) US20080139655A1 (es)
AR (1) AR062659A1 (es)
CL (1) CL2007002574A1 (es)
PE (1) PE20080669A1 (es)
WO (1) WO2008030830A2 (es)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101687781B1 (ko) 2008-08-15 2016-12-20 데포메드 인코퍼레이티드 Cns 장애의 치료 및 예방을 위한 위 체류성 약학적 조성물
US10022320B2 (en) 2014-03-13 2018-07-17 Neuroderm, Ltd. Dopa decarboxylase inhibitor compositions
US10258585B2 (en) 2014-03-13 2019-04-16 Neuroderm, Ltd. DOPA decarboxylase inhibitor compositions
ES2897024T3 (es) * 2017-03-01 2022-02-28 Arena Pharm Inc Composiciones que comprenden agonistas del receptor de PGI2 y procesos para la preparación de las mismas
CN109439645B (zh) * 2018-10-31 2022-07-19 武汉工程大学 利用锐孔法制备解磷微生物缓释海藻酸钠微球的方法
WO2020230089A1 (en) 2019-05-14 2020-11-19 Clexio Biosciences Ltd. Treatment of nocturnal symptoms and morning akinesia in subjects with parkinson's disease
WO2022005926A1 (en) * 2020-06-30 2022-01-06 Imbria Pharmaceuticals, Inc. Modified release formulations of modified forms of trimetazidine
US11213502B1 (en) 2020-11-17 2022-01-04 Neuroderm, Ltd. Method for treatment of parkinson's disease
US11331293B1 (en) 2020-11-17 2022-05-17 Neuroderm, Ltd. Method for treatment of Parkinson's disease
US11844754B2 (en) 2020-11-17 2023-12-19 Neuroderm, Ltd. Methods for treatment of Parkinson's disease
WO2022195476A1 (en) 2021-03-15 2022-09-22 Clexio Biosciences Ltd. Gastroretentive devices for assessment of intragastric conditions

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4424235A (en) * 1981-09-14 1984-01-03 Hoffmann-La Roche Inc. Hydrodynamically balanced controlled release compositions containing L-dopa and a decarboxylase inhibitor
ZA889189B (en) * 1986-06-16 1989-08-30 Merck & Co Inc Controlled release combination of carbidopa/levodopa
US5190763A (en) * 1990-05-07 1993-03-02 Alza Corporation Dosage form indicated for the management of abnormal posture, tremor and involuntary movement
IL133196A0 (en) * 1999-11-29 2001-03-19 Yissum Res Dev Co Gastroretentive controlled release pharmaceutical dosage forms
KR20030013460A (ko) * 2000-06-23 2003-02-14 테바 파마슈티컬 인더스트리즈 리미티드 치료제의 위 체류 및 방출 조절을 위한 급속 팽창성조성물과 이 조성물을 포함하는 제형
US6531153B2 (en) * 2001-05-29 2003-03-11 Drugtech Corporation Composition with sustained release of levodopa and carbidopa
CA2409552A1 (en) * 2001-10-25 2003-04-25 Depomed, Inc. Gastric retentive oral dosage form with restricted drug release in the lower gastrointestinal tract
US20030224045A1 (en) * 2002-05-29 2003-12-04 Chien-Hsuan Han Combination immediate release sustained release levodopa/carbidopa dosage forms
WO2004032906A1 (en) * 2002-10-11 2004-04-22 Depomed Development, Ltd. Gastro-retentive levodopa delivery form
US20040185097A1 (en) * 2003-01-31 2004-09-23 Glenmark Pharmaceuticals Ltd. Controlled release modifying complex and pharmaceutical compositions thereof

Also Published As

Publication number Publication date
US20080139655A1 (en) 2008-06-12
WO2008030830A3 (en) 2008-05-29
CL2007002574A1 (es) 2008-05-23
WO2008030830A2 (en) 2008-03-13
PE20080669A1 (es) 2008-07-18

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