Accu-Break, Alembic in new Accu-Break tablets development agreement
ABP said its patented Accu-Break tablets can be split easily by hand into exact smaller doses, which will make it easier and safer for patients and caregivers to
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).