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Phase 1 and 2 Randomized Clinical Studies Determine Lack of Efficacy for Anti-IL-17C Antibody MOR106 in Moderate-Severe Atopic Dermatitis.
Thaçi, Diamant; Singh, Dave; Lee, Mark; Timmis, Helen; Jacobs, Dominique; Passier, Paul; Rohrer, Susanne; Beetens, Johan; Phung, De; Sondag, Eric; Babic, Goran; Würth, Guido; Kloepfer, Pia; Härtle, Stefan; Hüttner, Silke.
Afiliación
  • Thaçi D; Institute and Comprehensive Center for Inflammation Medicine, University of Lübeck, 23538 Lübeck, Germany.
  • Singh D; Medicines Evaluation Unit, Manchester University NHS Foundation Trust, University of Manchester, Manchester M23 9LT, UK.
  • Lee M; Progressive Clinical Research, San Antonio, TX 78213, USA.
  • Timmis H; Galapagos, 2800 Mechelen, Belgium.
  • Jacobs D; Galapagos, 2800 Mechelen, Belgium.
  • Passier P; Galapagos, 2800 Mechelen, Belgium.
  • Rohrer S; Novartis Pharma AG, 4056 Basel, Switzerland.
  • Beetens J; Galapagos, 2800 Mechelen, Belgium.
  • Phung; Galapagos, 2800 Mechelen, Belgium.
  • Sondag E; Galapagos, 2800 Mechelen, Belgium.
  • Babic G; MorphoSys AG, 82152 Planegg, Germany.
  • Würth G; MorphoSys AG, 82152 Planegg, Germany.
  • Kloepfer P; MorphoSys AG, 82152 Planegg, Germany.
  • Härtle S; MorphoSys AG, 82152 Planegg, Germany.
  • Hüttner S; Galapagos, 2800 Mechelen, Belgium.
J Clin Med ; 11(23)2022 Dec 06.
Article en En | MEDLINE | ID: mdl-36498818
Interleukin 17C (IL-17C) modulates epithelial inflammation and has a possible role in atopic dermatitis (AD) pathology. Four randomized clinical studies (Phase 1 and 2) investigated the safety, tolerability, efficacy, and pharmacokinetic profile of the anti-IL-17C monoclonal antibody MOR106 for up to 12 weeks (NCT03568071: n = 207 adults with moderate-severe AD; NCT03689829 Part 1: n = 32 healthy males; NCT03689829 Part 2: n = 44 adults with moderate-severe AD; and NCT03864627: n = 76 adults with moderate-severe AD). In these studies, MOR106 was either administered intravenously (i.v.) every 2 or 4 weeks at doses between 1-10 mg/kg, or subcutaneously (s.c.), either as a single dose or doses every 2 weeks at 320 mg. Overall, MOR106 was well-tolerated, and the safety profile was consistent with monoclonal antibodies approved for AD. Bioavailability following s.c. dosing was 55%, and steady-state drug levels were reached at 2-4 weeks. Ongoing studies were terminated following a futility analysis of the Phase 2 placebo-controlled dose-finding study (NCT03568071) due to a low probability for achieving the primary efficacy endpoint. Cumulatively, MOR106 demonstrated ineffectiveness for the treatment of AD, but its safety and pharmacokinetic characteristics warrant further drug development in other indications. Funding: sponsored by Galapagos NV; funded by Novartis AG.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: J Clin Med Año: 2022 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: J Clin Med Año: 2022 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Suiza