drugset / Trial / NCT02263508

Pembrolizumab With Talimogene Laherparepvec or Placebo in Unresected Melanoma

NCT02263508

Phase 3 Terminated 713 enrolled Amgen Merck Sharp & Dohme LLC · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objectives of the Phase 1b part of the study are to evaluate the safety, as assessed by incidence of dose limiting toxicity (DLT), of talimogene laherparepvec in combination with pembrolizumab in adults with previously untreated, unresectable, stage IIIB to IVM1c melanoma. The primary objective of Phase 3 are to evaluate the efficacy of talimogene laherparepvec with pembrolizumab versus placebo with pembrolizumab, as assessed by progression-free survival (PFS) (response evaluation by blinded independent central review using modified Response Evaluation Criteria in Solid Tumors \[RECIST\] 1.1) and overall survival (OS).

Timeline

Start
2014-12-08
Primary completion
2021-03-11
Completion
2021-03-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Pembrolizumab Monoclonal antibody 200 mg Intravenous
Subject Talimogene Laherparepvec Other / unclassified 4 ml Other

Indications