Phase 2 Lymphoma Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You have been diagnosed with Mycosis Fungoides (MF), a type of skin lymphoma, confirmed by a tissue sample (biopsy), and it affects your skin.
- You have at least one skin lesion that can be seen and measured during a physical exam.
- If you were previously diagnosed with MF and have developed a new skin lesion, that new lesion may be eligible without needing another biopsy.
- Your skin lesion(s) are no taller than 1 cm (about the height of a small fingernail) when measured from the skin surface — and if you have multiple lesions meeting this requirement, each one may be enrolled separately.
- You have any stage of MF (from early to advanced) where radiation therapy is being considered to treat a specific lesion.
- You are currently receiving or planning to start a systemic (whole-body) treatment for more advanced disease.
- If you are a woman who could become pregnant, you have had a negative pregnancy blood test within the past 2 weeks, or you have signed a declaration confirming you are not pregnant.
- You are using or planning to use certain skin-based treatments (such as topical chemotherapy, retinoids, or imiquimod) on other lesions not being enrolled in the trial — as long as the lesion being enrolled has not had those treatments applied for at least 24 hours before joining the study.
Who may not be able to join:
- You are currently pregnant.
- You have been diagnosed with active lupus or scleroderma (certain autoimmune conditions).
- The skin lesion being considered for the trial is taller than 1 cm when measured from the skin surface.
- The lesion being considered for enrollment has had topical chemotherapy, retinoids, or imiquimod applied to it within the last 24 hours (confirm with trial site).
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Bouthaina S Dabaja, M.D. Anderson Cancer Center
Phone: 713-563-2300
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Local cutaneous control
Can't join this trial?
Data last synced from ClinicalTrials.gov: 5 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.