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Machine translation
1. (WO2002028375) A CONTROLLED-RELEASE, PARENTERALLY ADMINISTRABLE MICROPARTICLE PREPARATION
Latest bibliographic data on file with the International Bureau   

Pub. No.:    WO/2002/028375    International Application No.:    PCT/SE2001/002165
Publication Date: 11.04.2002 International Filing Date: 05.10.2001
Chapter 2 Demand Filed:    29.04.2002    
IPC:
A61K 9/16 (2006.01), A61K 38/17 (2006.01), A61K 38/27 (2006.01)
Applicants: JAGOTEC AG [CH/CH]; Eptingerstrasse 51 CH-4132 Muttenz (CH) (For All Designated States Except US).
RESLOW, Mats [SE/SE]; (SE) (For US Only).
BJÖRN, Sören [DK/DK]; (DK) (For US Only).
DRUSTRUP, Jörn [DK/DK]; (DK) (For US Only).
GUSTAFSSON, Nils, Ove [SE/SE]; (SE) (For US Only).
JÖNSSON, Monica [SE/SE]; (SE) (For US Only).
LAAKSO, Timo [SE/GB]; (GB) (For US Only)
Inventors: RESLOW, Mats; (SE).
BJÖRN, Sören; (DK).
DRUSTRUP, Jörn; (DK).
GUSTAFSSON, Nils, Ove; (SE).
JÖNSSON, Monica; (SE).
LAAKSO, Timo; (GB)
Agent: AWAPATENT AB; Box 45086 S-104 30 Stockholm (SE)
Priority Data:
0003614-5 06.10.2000 SE
60/260,495 08.01.2001 US
Title (EN) A CONTROLLED-RELEASE, PARENTERALLY ADMINISTRABLE MICROPARTICLE PREPARATION
(FR) PREPARATION DE MICROPARTICULES ADMINISTRABLES PAR VOIE PARENTERALE A LIBERATION REGULEE
Abstract: front page image
(EN)A parenterally administrable, biodegradable microparticle preparation, preferably composed of amylopectin-containing starch. The preparation contains a biologically active substance which, during the first 24 hours after injection, exhibits a release of the active substance that is less than 25 % of the total release, determined from a concentration-time curve in the form of the ratio between the area under the curve during the said first 24 hours and the total area under the curve in question.
(FR)L'invention concerne une préparation de microparticules biodégradables pouvant être administrées par voie parentérale composées de préférence d'amidon contenant de l'amylopectine. La préparation contient une substance bioactive qui, pendant les 24 heures suivant l'injection, présente une libération de la substance active inférieure à 25 % de la libération totale, déterminée à partir d'une courbe de concentration-temps se présentant sous la forme du rapport entre la zone située au-dessus de la courbe pendant les premières 24 hures et la zone totale située sous la courbe en question.
Designated States: AE, AG, AL, AM, AT, AU, AZ, BA, BB, BG, BR, BY, BZ, CA, CH, CN, CO, CR, CU, CZ, DE, DK, DM, DZ, EC, EE, ES, FI, GB, GD, GE, GH, GM, HR, HU, ID, IL, IN, IS, JP, KE, KG, KP, KR, KZ, LC, LK, LR, LS, LT, LU, LV, MA, MD, MG, MK, MN, MW, MX, MZ, NO, NZ, PH, PL, PT, RO, RU, SD, SE, SG, SI, SK, SL, TJ, TM, TR, TT, TZ, UA, UG, US, UZ, VN, YU, ZA, ZW.
African Regional Intellectual Property Organization (GH, GM, KE, LS, MW, MZ, SD, SL, SZ, TZ, UG, ZW)
Eurasian Patent Organization (AM, AZ, BY, KG, KZ, MD, RU, TJ, TM)
European Patent Office (AT, BE, CH, CY, DE, DK, ES, FI, FR, GB, GR, IE, IT, LU, MC, NL, PT, SE, TR)
African Intellectual Property Organization (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, GW, ML, MR, NE, SN, TD, TG).
Publication Language: English (EN)
Filing Language: English (EN)