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Viernes 2 oct 2026SEC · NASDAQ biomédico

Calendario›INCY›INCB028050

INCB028050

INCB028050 Compared to Background Therapy in Patients With Active Rheumatoid Arthritis (RA) With Inadequate Response to Disease Modifying Anti-Rheumatic Drugs

Ensayo de INCYTE CORP en Artritis reumatoide.

Más ensayos de: Artritis reumatoide.

Fase
Fase 2
Estado
Completado
Participantes
127
previstos
Centros
49
Fin del objetivo primario
jun 2010
fecha real

Qué significa cada fase y cada estado.

Estudio de intervención, aleatorizado, doble ciego. Comenzó en may 2009.

Qué mide

The Percentage of Participants Achieving American College of Rheumatology (ACR) 20 Improvement (del registro, en inglés) (semana 12)

Cómo lo describe el promotor

En el documentoEn inglés, del registroThis was a randomized, double blind, placebo controlled, dose ranging, parallel group study. Participants who had active rheumatoid arthritis (RA) who had inadequate response to any disease modifying anti-rheumatic drug (DMARD) therapy including biologics were enrolled. Screening evaluations were performed within approximately 28 days of randomization. The duration of the study was 6 months with the primary endpoint assessed at 3 months. Eligible participants were randomly assigned to one of three doses (4, 7 or 10 mg QD) of INCB028050 (Baricitinib) or placebo.

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Todos los de INCY, en su ficha.

Ficha completa en ClinicalTrials.gov (NCT00902486), actualizada en ago 2018.