Innovent Biologics Inc (HKEX: 01801), a biopharmaceutical company focused on treatment of oncologic, autoimmune, cardiovascular and metabolic, ophthalmologic and other major diseases, announced Thursday that the first participant has been successfully dosed in GLORY-3, a Phase 3 clinical study of mazdutide (Innovent R&D Code: IBI362).
Mazdutide is a dual glucagon (GCG) and glucagon-like peptide 1 receptor (GLP-1) receptor agonist for treating overweight or obesity accompanied metabolic dysfunction-associated fatty liver disease (MAFLD).
GLORY-3 is a multi-centre, randomised, open-label Phase 3 clinical study comparing the efficacy and safety of mazdutide versus semaglutide in Chinese adults with overweight or obesity accompanied MAFLD. The study is planned to enrol approximately 470 participants, randomised 1:1 to receive mazdutide 9 mg or semaglutide 2.4 mg.
Innovent has entered into an exclusive licence agreement with Eli Lilly and Company (NYSE:LLY) for the development and potential commercialisation of OXM3 (mazdutide), which may offer additional benefits beyond those of GLP-1 receptor agonists -- such as promoting insulin secretion, lowering blood glucose and reducing body weight -- by activating the glucagon receptor to increase energy expenditure and improve hepatic fat metabolism.
Accord Healthcare introduces Dehydrated Alcohol Injection for cardiovascular indications
Innovent presents mazdutide Phase 3 clinical study results at ADA 85th Scientific Sessions
Breckenridge Pharmaceutical's generic for Ablysinol granted final FDA approval
Cumberland Pharmaceuticals reports ifetroban Phase 2 DMD heart disease trial results
EDX Medical and Spire Healthcare sign strategic diagnostic partnership agreement
Bayer and Broad Institute extend cardiovascular research alliance to advance precision therapies
CirCode Biomed's IND application for HM2002 receives FDA clearance