drugset / Trial / NCT01796002

Efficacy and Safety of Romidepsin CHOP vs CHOP in Patients With Untreated Peripheral T-Cell Lymphoma

NCT01796002 ↗

Phase 3 Completed 421 enrolled The Lymphoma Academic Research Organisation
RandomizedParallel-groupOpen-labelTreatment

Summary

Primary objective of the study is to compare the efficacy of romidepsin when administered with CHOP versus CHOP alone in subjects with previously untreated peripheral T-cell lymphoma (PTCL) in terms of progression-free survival (PFS) assessed according to Response criteria for malignant lymphoma 1999 by a Response Adjudication Committee (RAC).

Timeline

Start
2013-01
Primary completion
2019-12-13
Completion
2022-12-13

Outcome

Missed primary endpoint

paper The addition of romidepsin to CHOP did not improve PFS, response rates, nor overall survival PMID 34843406 ↗

release “confirmatory Phase 3 study evaluating romidepsin plus CHOP (Ro-CHOP) versus CHOP in first-line PTCL patients, but the trial did not meet the primary efficacy endpoint” bms.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Romidepsin Peptide 12 mg/m2 Intravenous
Background Cyclophosphamide Other / unclassified — —
Background Doxorubicin Other / unclassified — —
Background Prednisone Other / unclassified — —
Background Vincristine Small molecule — —