Clinical trial
Phase 1/2 Study to Evaluate the Safety, Feasibility, and Efficacy of FP-1201 (Intravenous Interferon-Beta-1a) to Prevent Toxicities After CD19-Directed CAR T-Cell Therapy
NCT05936229 is registered in ClinicalTrials.gov with Fred Hutchinson Cancer Center as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Phase 1/2 Study to Evaluate the Safety, Feasibility, and Efficacy of FP-1201 (Intravenous Interferon-Beta-1a) to Prevent Toxicities After CD19-Directed CAR T-Cell Therapy
- Lead sponsor
- Fred Hutchinson Cancer Center
- Phase
- Phase 1/2
- Overall status
- Withdrawn
- Start date
- April 1, 2025
- Completion date
- October 30, 2027
- Enrollment
- 0 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
recurrent b acute lymphoblastic leukemia, recurrent b-cell non-hodgkin lymphoma, recurrent mantle cell lymphoma, refractory b acute lymphoblastic leukemia, refractory b-cell non-hodgkin lymphoma, refractory mantle cell lymphoma