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Unicycive Therapeutics (Nasdaq: UNCY) announced that the FDA has accepted the resubmission of its New Drug Application (NDA) for oxylanthanum carbonate (OLC), the company’s investigational oral phosphate binder for the treatment of hyperphosphatemia in patients with chronic kidney disease (CKD) on dialysis. The FDA deemed the resubmission a Class II complete response, resulting in a six-month review period, and assigned a PDUFA target action date of June 29, 2026. Unicycive Therapeutics is a B2i
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