
Five-pathway obesity drug outperforms Ozempic in mice, signaling a multi-target therapy future
Munich researchers engineered a single molecule that activates five metabolic targets (GLP-1, GIP, plus three internal PPAR switches) with gut-targeted delivery. In obese mice it reduced appetite, body fat, and weight more than semaglutide (Ozempic) and a GLP-1/GIP co-agonist, while also improving blood sugar control and lowering liver fat/inflammation without the usual lanifibranor-side effects; if results translate to humans, this could pave the way for a weekly, five-target obesity therapy, though clinical trials will take years.













