CRISPR Therapeutics has faced challenges in the market, with its stock declining over the past three years.
Despite this, the company has recently received regulatory approvals for its gene-editing medicine, Casgevy, which targets sickle cell disease (SCD) and transfusion-dependent beta-thalassemia (TDT).
However, the high cost of the treatment raises concerns about affordability for patients.
The Biden administration has announced a plan to improve access to Casgevy for Medicaid patients, which is expected to expand access to the therapy.
CRISPR Therapeutics reported low revenue for the year, but analysts project significant sales potential for Casgevy.
The company faces competition from other biotech firms, but its partnership with Vertex Pharmaceuticals and successful development of Casgevy position it well in the market.
Despite current stock performance, CRISPR Therapeutics' innovative approach to gene editing and government initiatives may lead to recovery and expansion in the future.