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Clinical Trial Summary

This is a Phase 1b, single-center, open-label study, evaluating efficacy and safety of RP1 for the treatment of resectable cutaneous Squamous Cell Carcinoma in up to 12 evaluable patients. In this study, patients will receive RP1 via direct intratumoral (IT) injection into superficial cutaneous solid tumors to assess the safety and tolerability as well efficacy of RP1 treatment. The primary efficacy population is up to 12 evaluable patients with resectable CSCC. The enrollment of patients with CSCC will determine study duration.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05858229
Study type Interventional
Source Rochester Dermatologic Surgery
Contact Sherrif Ibrahim, MD. PhD
Phone 5852221400
Email dr.ibrahim@rochesterdermsurgery.com
Status Recruiting
Phase Phase 1/Phase 2
Start date June 16, 2023
Completion date June 2026

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