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.
GE HealthCare's Photonova Spectra gains FDA clearance
Nuwellis completes Rendiatech acquisition
HeartBeam and Mount Sinai partner to advance AI-enabled cardiac monitoring
Medicomp Systems client IJN in Malaysia granted Stage 7 validation from HIMSS EMRAM
Precision BioSciences receives FDA Fast Track designation for PBGENE-DMD
GAIA and Daiichi Sankyo Europe partner on digital therapeutic for cardiovascular care
Esperion to acquire Corstasis, expanding cardiovascular portfolio
Circio reports up to 50-fold gene expression gain in eye for circVec-AAV platform