Roche’s Chlamydia test wins European approval
The test is designed with a dual target approach to help ensure reliability of test results even when mutations occur in the bacteria’s cryptic plasmid DNA. The highly
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).