[EN] STAT3 TRANSCRIPTION FACTOR INHIBITORS AND METHODS OF USING THE SAME [FR] INHIBITEURS DU FACTEUR DE TRANSCRIPTION STAT3 ET LEURS PROCÉDÉS D'UTILISATION
STAT3 TRANSCRIPTION FACTOR INHIBITORS AND METHODS OF USING THE SAME
申请人:The Regents of the University of Colorado, a body
corporate
公开号:EP3891132A2
公开(公告)日:2021-10-13
SALICYLANILIDES ENHANCE ORAL DELIVERY OF THERAPEUTIC PEPTIDES
申请人:Fogelman Alan M.
公开号:US20090163408A1
公开(公告)日:2009-06-25
This invention pertains to the surprising discovery that salicylanilides, e.g., niclosamide and/or niclosamide analogues when orally administered in conjunction with a peptide pharmaceutical (e.g., a class A amphipathic helical peptide as described herein) significantly increases the bioavailability of that peptide. Methods of peptide delivery using such “delivery agents” and pharmaceutical formulations are provided.
SALICYLANILIDE MODIFIED PEPTIDES FOR USE AS ORAL THERAPEUTICS
申请人:Fogelman Alan M.
公开号:US20110183889A1
公开(公告)日:2011-07-28
This invention pertains to the surprising discovery that salicylanilides, e.g., niclosamide and/or niclosamide analogues can be reacted with a therapeutically active peptide to produce a modified peptide complex that shows increased resistance to proteolysis and that shows higher bioactivity when orally administered than the unmodified peptide.
US8148328B2
申请人:——
公开号:US8148328B2
公开(公告)日:2012-04-03
[EN] SALICYLANILIDES ENHANCE ORAL DELIVERY OF THERAPEUTIC PEPTIDES<br/>[FR] LES SALICYLANILIDES RENFORCENT L'ADMINISTRATION PAR VOIE ORALE DE PEPTIDES THÉRAPEUTIQUES
申请人:UNIV CALIFORNINA
公开号:WO2008021088A2
公开(公告)日:2008-02-21
[EN] This invention pertains to the surprising discovery that salicylanilides, e.g., niclosamide and/or niclosamide analogues when orally administered in conjunction with a peptide pharmaceutical (e.g., a class A amphipathic helical peptide as described herein) significantly increases the bioavailability of that peptide. Methods of peptide delivery using such "delivery agents" and pharmaceutical formulations are provided. [FR] La présente invention concerne la découverte surprenante que l'administration par voie orale de salicylanilides, notamment la niclosamide et/ou certains de ses analogues, en association avec un peptide pharmaceutique tel qu'un peptide hélicoïdal amphipathique de classe A tel que décrit ici, augmente notablement la biodisponibilité de ce peptide. L'invention concerne également, d'une part des procédés d'administration de ces peptides au moyen d'agents d'administration, et d'autre part des formulations pharmaceutiques correspondantes.