drugset / Trial / NCT03291002

Study of Intratumoral CV8102 in cMEL, cSCC, hnSCC, and ACC

NCT03291002

Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study evaluates intratumoral administration of CV8102 in patients with advanced melanoma, squamous cell carcinoma of the skin, squamous cell carcinoma of the head and neck, or adenoid cystic carcinoma. Patients will receive CV8102 as single agent or in combination with SoC anti-PD-1 therapy.

Timeline

Start
2017-09-25
Primary completion
2022-10
Completion
2023-02

Drugs

EvaluationDrugModalityDoseRoute
Subject CV8102 Other / unclassified 600 ug Intrathecal
Subject CV8102 Other / unclassified 900 ug Intrathecal