drugset / Trial / NCT02574260

An Extension Protocol for the Extended Use of Talimogene Laherparepvec for Eligible Patients Who Participated in Study 002/03 (NCT00289016)

NCT02574260

Phase 2 Completed 3 enrolled BioVex Limited Covance · collab
NaSingle-groupOpen-labelTreatment

Summary

The primary objective of this extension study was to further assess the safety and tolerability of talimogene laherparepvec. Secondary objectives were to assess objective tumor response rate and survival.

Timeline

Start
2008-08
Primary completion
2010-01
Completion
2010-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Talimogene Laherparepvec Other / unclassified 1e+08 unknown Other

Indications