Oriel Therapeutics granted new US patent
The invention addresses the field of dry powder inhalers, and more specifically the drug containment systems (DCS) necessary for containment, protection and delivery of dry powder medicaments. Materials,
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).
The international, double-blind, placebo-controlled safety and efficacy study of oral Dimebon is known as the Connection study. The Connection study will enroll approximately 525 patients with mild-to-moderate Alzheimer’s