HomeTrialNCT06615635
🔬NCT06615635NARECRUITING

Alpha Radiation Emitters Device (DaRT) for the Treatment of Cutaneous SCC for Immunocompromised Patients

Study Summary

This is a multi-center clinical study enrolling up to 28 participants. The primary objectives are to determine the objective response rate (ORR) established by the confirmed best overall response (BOR) following intratumoral administration of DaRT - Diffusing Alpha-Emitters Radiation Therapy. Secondary objectives are to: 1. Determine Progression Free Survival (PFS) up to 12 months after Alpha DaRT sources insertion. 2. Assess Overall Survival (OS) of patients treated with DaRT up to 12 months. 3. Assess Local control up to 12 months after DaRT insertion.

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment28 participants
Primary Completion
Lead SponsorAlpha Tau Medical LTD.
Data Retrieved2026-06-17 02:56:49.846114+00:00
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