drugset / Trial / NCT03945019

CT-P13 (Infliximab) Subcutaneous Administration in Patients With Moderately to Severely Active Crohn's Disease (LIBERTY-CD)

NCT03945019 ↗

Phase 3 Completed 396 enrolled Celltrion
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is Phase 3, Randomized, Placebo-controlled study to demonstrate superiority of CT-P13 SC over Placebo SC in Patients With Moderately to Severely Active Crohn's Disease

Timeline

Start
2019-10-28
Primary completion
2022-08-23
Completion
2023-08-22

Outcome

Met primary endpoint

paper statistically significant higher proportions of CT-P13 SC-treated patients vs placebo-treated patients achieved clinical remission (62.3% vs 32.1%; P < .0001) PMID 38788861 ↗

paper endoscopic response (51.1% vs 17.9%; P < .0001). PMID 38788861 ↗

release “Based on the results of the LIBERTY UC and LIBERTY CD studies, ZYMFENTRA demonstrated superiority in the primary endpoints of clinical remission (UC and CD)” celltrion.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Infliximab Monoclonal antibody 120 mg Subcutaneous

Indications