drugset / Trial / NCT05188729

Summary

This is a 2-part, open-label, multicenter, dose-escalation, proof-of-concept study with a safety run-in designed to assess the safety, tolerability, MTD, and objective antitumor efficacy of ascending dose strengths of VP-315 when administered intratumorally to adults with biopsy proven basal cell carcinoma (BCC). The study is expected to enroll approximately 86 subjects with a histological diagnosis of BCC in at least 1 eligible target lesion (confirmed by punch or shave biopsy).

Timeline

Start
2022-02-01
Primary completion
2024-04-15
Completion
2024-04-15

Drugs

EvaluationDrugModalityDoseRoute
Subject VP-315 Unknown 2 mg Other
Subject VP-315 Unknown 3 mg Other
Subject VP-315 Unknown 4 mg Other
Subject VP-315 Unknown 5 mg Other
Subject VP-315 Unknown 6 mg Other
Subject VP-315 Unknown 7 mg Other
Subject VP-315 Unknown 8 mg Other