drugset / Trial / NCT02014441

Single-arm Trial to Evaluate the Biodistribution and Shedding of Talimogene Laherparepvec

NCT02014441

Phase 2 Completed 61 enrolled Amgen
NaSingle-groupOpen-labelTreatment

Summary

The primary objective was to estimate the proportion of participants with detectable talimogene laherparepvec deoxyribonucleic acid (DNA) in the blood and urine at any time after administration of talimogene laherparepvec within the first 3 cycles.

Timeline

Start
2014-04-07
Primary completion
2016-01-25
Completion
2018-04-19

Drugs

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

Indications