Fulcrum Therapeutics can resume testing its oral capsule in a Phase Ib study in patients with sickle cell disease, the biotech said Tuesday morning.
The FDA lifted the full clinical hold on FTX-6058, with trial revisions to focus on sicker patients after the small molecule spent six months in the waiting zone. The study protocol now stipulates patients must have severe cases of the red blood cell disorder or lack access to advanced therapies, either due to availability limitations or insurance hindrances. The trial was originally designed as an all-comers study.
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