Cell

Changing Obesity: Progress in Drugs Targeting Multiple Body Receptors

Updated

Abstract

Gut-hormone polyagonists may achieve weight reductions of up to 20%-30%.

  • GLP-1-based polyagonists target multiple hormone receptors to promote weight loss.
  • These treatments may also improve blood sugar levels and conditions like fatty liver and kidney disease.
  • Potential cardiovascular benefits are associated with these new pharmacological interventions.
  • This approach offers a non-surgical alternative to bariatric surgery for weight management.

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Funding

Competing interests

Declaration of interests C.M.K. and P.E.S. have sponsored research agreements with Eli Lilly. M.H.T. was a member of the Research Cluster Advisory Panel (ReCAP) of the Novo Nordisk Foundation between 2017 and 2019. He received funding for his research projects by Novo Nordisk (2016–2020) and Sanofi-Aventis (2012–2019). He consulted twice for Boehringer Ingelheim Pharma GmbH & Co. KG (2020 and 2021) and delivered a scientific lecture for Sanofi-Aventis Deutschland GmbH (2020). As CEO and CSO of Helmholtz Munich, he is co-responsible for numerous collaborations of the employees with a multitude of companies and institutions worldwide. In this capacity, he discusses potential projects with and has signed/signs contracts for the Helmholtz institute(s) related to research collaborations worldwide, including but not limited to pharmaceutical corporations like Boehringer Ingelheim, Novo Nordisk, Roche Diagnostics, Arbormed, Eli Lilly, SCG Cell Therapy, and others. As the CEO and CSO of Helmholtz Munich, he was/is further overall responsible for commercial technology transfer activities. M.H.T. confirms that, to the best of his knowledge, none of the above funding sources or collaborations were involved in or had an influence on the preparation of this manuscript. M.H.T. is a former member of the scientific advisory board of ERX, which is developing celastrol, but has no current competing interests. R.D.D. is the co-inventor of multiple patents pertaining to this field that are owned by Indiana University. He was co-founder of Marcadia Biotech and a former employee at Eli Lilly Research labs and Novo Nordisk, advancing drug candidates associated with the subject of this review. T.D.M. receives research funding from Novo Nordisk; however, these funds are unrelated to the work described here. T.D.M. further received speaking fees within the past 3 years from Novo Nordisk, Eli Lilly, AstraZeneca, Merck, Berlin Chemie AG, and Mercodia.
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