Semafore reports positive interim results from Phase I cancer trial
The data from the solid tumor trial demonstrate that SF1126 is well-tolerated in a twice-weekly IV infusion at exposure levels that have been shown to be active in
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).