Sarepta Therapeutics Provides Clarifying Statement on ELEVIDYS
1. FDA investigating death of patient after ELEVIDYS gene therapy. 2. Sarepta confirms death was deemed unrelated to the therapy.
1. FDA investigating death of patient after ELEVIDYS gene therapy. 2. Sarepta confirms death was deemed unrelated to the therapy.
The investigation indicates potential safety concerns which can deter investors. Historical instances such as the FDA scrutiny of other gene therapies have led to price declines.
The investigation could reflect poorly on SRPT's products, impacting investor confidence and stock performance.
Immediate market reactions to safety concerns typically occur, but longer-term effects depend on further investigation outcomes.