Stoke Therapeutics reported revenue of $4.8 million and a net loss of $25.7 million for the second quarter of 2024. The FDA removed the Partial Clinical Hold as the company advances toward a Phase 3 registrational study of zorevunersen.
FDA removed Partial Clinical Hold on zorevunersen.
Company plans to share data from Phase 1/2a and OLE studies of zorevunersen at the 15th European Epilepsy Congress in September 2024.
Company is on track to provide a regulatory update on Phase 3 registrational plans for zorevunersen in the second half of 2024.
Company is on track to initiate the Phase 1 study (OSPREY) of STK-002 for the treatment of Autosomal Dominant Optic Atrophy (ADOA) this year.
The company plans to share previously presented positive data from patients treated in the Phase 1/2a and open label extension (OLE) studies of zorevunersen in children and adolescents with Dravet syndrome at the 15th European Epilepsy Congress (EEC), September 7 – 11, 2024, in Rome, Italy. The company is on track to initiate the Phase 1 study (OSPREY) of STK-002 for the treatment of Autosomal Dominant Optic Atrophy (ADOA) this year.