An investigational study to assess the safety and effectiveness of a new investgational drug in people with moderately to severely active Ulcerative Colitis

Mise à jour : Il y a 4 ans
Référence : EUCTR2014-005217-24

Femme et Homme

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Extrait

• To evaluate the efficacy of GS-5745 to induce EBS clinical remission at Week 8 (Cohort 1) • To evaluate the efficacy of GS-5745 to maintain EBS clinical remission at Week 52 (Cohort 2) • To evaluate the safety and tolerability of GS-5745


Critère d'inclusion

  • Ulcerative colitis