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Clinical Trial Summary

This is a Phase 2 study designed to determine the preliminary anti-tumor activity and confirm the safety of VV1 in combination with cemiplimab. The study will enroll patients with three distinct separate tumor cohorts. The cancers types are colorectal, head and neck carcinoma, and melanoma that are progressing on CPI treatment.


Clinical Trial Description

Patients enrolled into three parallel doublet cohorts with an optimal Simon's two stage design. Patients will receive Voyager V1 as a direct to tumor injection (IT) in all 3 cancer groups and cemiplimab via IV infusion. Patients will return for treatment every 3 weeks until lack of clinical benefit or limiting toxicity. Efficacy evaluations will be conducted every 6 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04291105
Study type Interventional
Source Vyriad, Inc.
Contact Jennifer boughton
Phone 9085533135
Email Jboughton@vyriad.com
Status Recruiting
Phase Phase 2
Start date April 24, 2020
Completion date March 2025

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