Clinical Trial SuccessUnicycive announced the successful completion of the UNI-494 Phase 1 study in healthy volunteers, with UNI-494 overall well-tolerated in single doses up to 160 mg and multiple doses of 40 mg twice daily.
Product DifferentiationOLC's small pill size and ability to be taken without chewing are two differentiating attributes that make it an attractive treatment option among phosphate binders.
Regulatory MilestoneThe NDA for OLC was accepted for review by FDA with a PDUFA date, presenting a significant opportunity for Unicycive.