drugset / Trial / NCT05672199

Long-term Safety and Efficacy of Efavaleukin Alfa in Participants With Moderately to Severely Active Ulcerative Colitis

NCT05672199 ↗

Phase 2 Terminated 25 enrolled Amgen
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to evaluate the long-term safety and tolerability of efavaleukin alfa in participants with moderate to severe ulcerative colitis (UC).

Timeline

Start
2023-04-28
Primary completion
2024-10-31
Completion
2024-10-31

Outcome

Outcome not reported

Stopped: “The parent study 20170104 was terminated due to the study meeting a prespecified futility rule. Consequently, this study was terminated.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Efavaleukin alfa Protein / enzyme biologic — Subcutaneous

Indications