May 14, 2025
Preclinical results presented at ECO 2025 and demonstrate clinical potential of Myo4 compared with current GLP-1 treatment alternatives
Harwell, Oxford, May 14, 2025, ¶¶Òõapp (¶¶Òõapp), today announces results for its novel small molecule Myo4 targeting obesity. In the diet induced obesity (DIO) mouse model, Myo4 reduced weight while preserving muscle and bone mineral content. These results are being presented by ¶¶Òõapp’s co-founder, Professor Matt Whiteman, at the 32nd European Congress on Obesity.
The presentation is entitled: ‘The novel small molecule Myo4 normalises glycemic control, reduces weight/fat mass and prevents semaglutide-induced muscle remodeling in the murine diet-induced obesity model’. The effect was seen with Myo4 as monotherapy. Myo4 also provided additional weight loss with muscle preservation when used in combination with semaglutide. The data also showed that Myo4 treated mice had better preserved bone mineral content compared to semaglutide treated animals. This is achieved by a novel mitochondrial metabolic mechanism of action. This therapeutic route is entirely separate from the current standard GLP-1 agonist treatment for obesity, which decreases muscle as well as fat.
There are currently nearly 890 million people living with obesity worldwide, with 1.6 billion adults with overweight based on body mass index (BMI) category. The global economic impact of obesity is expected to be over USD 4 trillion by 2035, and USD 18 trillion by 2060.
“These preclinical results confirm that the small molecule Myo4 has the potential to maintain lean muscle mass whilst reducing fat. These data demonstrate the potential of Myo4 to vastly increase the quality of weight loss over current GLP-1 options,†said Xavier Jacq, CSO, ¶¶Òõapp. “This will enable ¶¶Òõapp to move towards clinical preparation for Myo4 and develop a viable solution for obesity patients with greatly reduced side effects.â€
“GLP-1 treatments have revolutionized the treatment of obesity, but they are not without their drawbacks,†said Jon Rees, CEO, ¶¶Òõapp. “With its entirely new mechanism of action, ¶¶Òõapp’s discovery of Myo4 provides a new solution addressing the underlying cause of metabolic disease with the potential to lead the next generation of improved treatments for weight loss leading to better health.â€
About Myo4 and other platform compounds
Myo4 was developed by ¶¶Òõapp as an improved mitochondrial-targeted persulfide modifier. These results enable ¶¶Òõapp to move Myo4 as our lead toward clinical candidate nomination. ¶¶Òõapp has an expanding library of compounds with severable IP for different indications.
For more information please contact:
Neil Hunter
Hunter PR
neiljameshunter@gmail.com
+44 7821 255568
About ¶¶Òõapp
¶¶Òõapp’s mission is to develop a new class of medicines restoring normal metabolism by correcting impaired sulfide-signaling in mitochondria. Our lead programs are in cardiometabolism using novel mitochondrial-targeted persulfide modifiers. The most advanced indication is in the treatment of obesity building on the work of academic co-founder, Prof Matt Whiteman and his academic collaborators around the world. ¶¶Òõapp is based in Harwell Oxford and has raised USD 8 million in seed financing from investors including the UK Innovation & Science Seed Fund, the Fink Family Office, Wren Capital, Oxford Technology Management, Empirical Ventures, the Science Angel Syndicate Network, Panacea Innovation Ventures, Longevitytech.fund, as well as angel investors. For more information visit the website at mitorxtherapeutics.com and follow ¶¶Òõapp on LinkedIn.