CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 72 enrolled
Drug / intervention
Talimogene laherparepvec +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04068181
NCT04068181Phase 2Completed

Phase 2 Study of Talimogene Laherparepvec in Combination With Pembrolizumab in Subjects With Unresectable/Metastatic Stage IIIB-IVM1d Melanoma Who Have Progressed on Prior Anti PD-1 Based Therapy

Amgen·interventional·Posted Aug 28, 2019·Updated Jan 7, 2025

In Brief

A Phase 2 clinical trial evaluating Talimogene laherparepvec and Pembrolizumab for Melanoma. Completed, enrolled 72 participants across 46 sites in 11 countries.

Detailed Summary

This is a phase 2, open-label, single-arm, multicenter clinical trial designed to evaluate the efficacy and safety of talimogene laherparepvec in combination with pembrolizumab following disease progression on prior anti-programmed cell death protein (anti-PD-1) therapy in unresectable/metastatic melanoma (stage IIIB-IVM1d) or prior anti-PD-1 therapy in the adjuvant setting. Subjects will be treated with talimogene laherparepvec and pembrolizumab until confirmed complete response, disappearance of all injectable lesions, documented confirmed disease progression per modified immune-related Response Criteria simulating Response Evaluation Criteria in Solid Tumors (irRC-RECIST), intolerance of study treatment, or 102 weeks from the first dose of talimogene laherparepvec and/or pembrolizumab, whichever occurs first.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMelanoma
CountriesAustralia, Canada, France, Germany, Greece, Italy, Netherlands, Poland, Spain, United Kingdom, United States

Timeline

Phase 2CompletedFinished
2020202120222023202420252026
First PostedAug 28, 2019
Enrollment StartJan 22, 2020
Primary CompletionAug 19, 2021
Study CompletionFeb 26, 2024
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 6.8 years ago

Interventions

Talimogene laherparepvecdrug

Intralesional injection into injectable cutaneous, subcutaneous and nodal legions.

Pembrolizumabdrug

Intravenous (IV) infusion.