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Study identifier: NCT06615635 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Squamous Cell Carcinoma · Alpha Radiation · Immunocompromised  ·  Sponsor: Alpha Tau Medical LTD.

PhaseNA
Planned participants28
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Liron Dimnik  ·  +972-2-3737-210  ·  LironD@alphatau.com

Aviya Hoida  ·  +972-2-3737-210  ·  aviyah@alphatau.com

Always discuss trial participation with your own doctor first.

Locations (11)

Banner HealthGilbert, Arizona, United StatesRecruiting
Us Dermatology ParthnersPhoenix, Arizona, United StatesRecruiting
Alliance DermatologyPhoenix, Arizona, United StatesRecruiting
Integrity Research Clinical AssociatesBoca Raton, Florida, United StatesNot Yet Recruiting
Hollywood DermatologyHollywood, Florida, United StatesRecruiting
Palm Beach Dermatology GroupPalm Beach, Florida, United StatesNot Yet Recruiting
Day Star Skin Cancer CenterPoinciana, Florida, United StatesNot Yet Recruiting
Emory UniversityAtlanta, Georgia, United StatesRecruiting
Mayo ClinicRochester, Minnesota, United StatesNot Yet Recruiting
Bassett HealthcareCooperstown, New York, United StatesRecruiting
Hadassah Medical CenterJerusalem, IsraelNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT06615635