drugset / Trial / NCT03345836

A Study of the Efficacy and Safety of Upadacitinib (ABT-494) in Participants With Moderately to Severely Active Crohn's Disease Who Have Inadequately Responded to or Are Intolerant to Biologic Therapy

NCT03345836 ↗

Phase 3 Completed 624 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objective of this study is to evaluate the efficacy and safety of upadacitinib compared to placebo as induction therapy in participants with moderately and severely active Crohn's disease (CD).

Timeline

Start
2017-11-29
Primary completion
2021-08-11
Completion
2021-08-11

Outcome

Met primary endpoint

registry analysis (superiority test); Part 1 (Double Blind): Placebo vs Part 1 (Double Blind): Upadacitinib 45 mg; p <0.0001; Adjusted Risk Difference 17.9 (95% CI 10.0 to 25.8) NCT03345836 ↗

registry analysis (superiority test); Part 1 (Double Blind): Placebo vs Part 1 (Double Blind): Upadacitinib 45 mg; p <0.0001; Adjusted Risk Difference 31.2 (95% CI 25.5 to 37.0) NCT03345836 ↗

release “today announced positive top-line results from U-EXCEED, a Phase 3 induction study, showing upadacitinib (45 mg once daily) achieved both primary endpoints” abbvie.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Upadacitinib Small molecule 30 mg Oral
Subject Upadacitinib Small molecule 45 mg Oral

Indications