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 granted priority review to Roche’s supplemental biologics licence application (sBLA) for Gazyva/Gazyvaro (obinutuzumab) to treat adults with primary membranous nephropathy (pMN).