drugset / Trial / NCT02285062

Efficacy and Safety Study of Lenalidomide Plus R-CHOP Chemotherapy Versus Placebo Plus R-CHOP Chemotherapy in Untreated ABC Type Diffuse Large B-cell Lymphoma

NCT02285062 ↗

Phase 3 Completed 570 enrolled Celgene Corporation
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To evaluate the efficacy and safety of lenalidomide, rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R2-CHOP) chemotherapy versus placebo, rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (placebo-R-CHOP) chemotherapy in patients who have previously untreated ABC type DLBCL.

Timeline

Start
2015-02-17
Primary completion
2019-03-15
Completion
2022-07-28

Outcome

Missed primary endpoint

registry p = 0.2864; Hazard Ratio (HR) 0.849 (95% CI 0.632 to 1.140); Log Rank NCT02285062 ↗

paper The primary end point of PFS was not met, with a hazard ratio of 0.85 (95% CI, 0.63 to 1.14) and P = .29; PMID 33621109 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenalidomide Other / unclassified 15 mg Oral
Background Cyclophosphamide Other / unclassified — —
Background Doxorubicin Other / unclassified — —
Background Prednisone Other / unclassified — —
Background Rituximab Monoclonal antibody — —
Background Vincristine Small molecule — —