Akashi gets FDA nod to restart clinical development of DMD drug HT-100
Akashi plans to initiate a new study, HALO-DMD-04. “We are pleased to learn that the FDA is allowing Akashi to resume the clinical development of HT-100,” said Pat
The US Food and Drug Administration (FDA) has declined to approve Unicycive Therapeutics’ resubmitted new drug application (NDA) for oxylanthanum carbonate (OLC) to treat hyperphosphatemia in chronic kidney disease (CKD) patients on dialysis.