Study #2023-0470
A phase 1a/1b trial in Relapsed/Refractory T-cell Non-Hodgkin Lymphoma to determine the safety profile, pharmacology, and maximum tolerated dose of ST-001, a Fenretinide Phospholipid suspension (12.5 mg/mL) for IV infusion
MD Anderson Study Status
Enrolling
Treatment Agent
Fenretinide
Description
This study evaluates a fenretinide phospholipid suspension for the treatment of T-cell non-Hodgkin's lymphoma (NHL).
Resources and Links
Phone Number: 1-877-MDA-6789
Information and next steps
Disease:
T-cell Lymphoma, Cutaneous/Peripheral T-Cell Lymphoma, Peripheral T-cell Lymphoma, Peripheral T-Cell Lymphoma, Not Classified, Primary Cutaneous T-cell Lymphoma, Cutaneous T-Cell Lymphoma, Unspecified, Cutaneous T-cell Lymphoma, Follicular T-Cell Lymphoma, Angioimmunoblastic T-cell Lymphoma, Sézary's Disease, Mycosis Fungoides
Study phase:
Phase I
Physician name:
Auris Huen
Department:
Dermatology
For general questions about clinical trials:
1-844-994-3163
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