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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03291002
Study type Interventional
Source CureVac AG
Contact
Status Active, not recruiting
Phase Phase 1
Start date September 25, 2017
Completion date February 2023

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