FOXG1 Research Foundation

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FDA Clears FOXG1 Gene Therapy FRF-001 for Clinical Trials

The U.S. Food and Drug Administration has approved an Investigational New Drug application for FRF-001, a viral gene therapy for FOXG1 syndrome developed at the University at Buffalo. The first-in-human trial will be independently sponsored by the FOXG1 Research Foundation.

Related Clinical Trials

NCT ID Title Status Phase
NCT07293546

Phase 1/2 Study of FRF-001, an AAV-9 Gene Therapy, in Patients With FOXG1 Syndrome (FS)

NOT_YET_RECRUITING PHASE1/PHASE2