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Cotadutide promotes glycogenolysis in people with overweight or obesity diagnosed with type 2 diabetes

Parker, Victoria E. R. (author)
AstraZeneca, England
Robertson, Darren (author)
AstraZeneca, England
Erazo-Tapia, Edmundo (author)
Maastricht Univ Med Ctr, Netherlands
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Havekes, Bas (author)
Maastricht Univ Med Ctr, Netherlands
Phielix, Esther (author)
Maastricht Univ Med Ctr, Netherlands
de Ligt, Marlies (author)
Maastricht Univ Med Ctr, Netherlands
Roumans, Kay H. M. (author)
Maastricht Univ Med Ctr, Netherlands
Mevenkamp, Julian (author)
Maastricht Univ Med Ctr, Netherlands
Sjöberg, Folke, 1956- (author)
Linköpings universitet,Avdelningen för kirurgi, ortopedi och onkologi,Medicinska fakulteten,Region Östergötland, Hand- och plastikkirurgiska kliniken US,Clin Trial Consultants AB, Sweden
Schrauwen-Hinderling, Vera B. (author)
Maastricht Univ Med Ctr, Netherlands
Johansson, Edvin (author)
Antaros Med AB, Sweden
Chang, Yi-Ting (author)
AstraZeneca, MD 20878 USA
Esterline, Russell (author)
AstraZeneca, MD USA
Smith, Kenneth (author)
Univ Nottingham, England
Wilkinson, Daniel J. (author)
Univ Nottingham, England
Hansen, Lars (author)
AstraZeneca, Sweden
Johansson, Lars (author)
Antaros Med AB, Sweden
Ambery, Philip (author)
AstraZeneca, Sweden
Jermutus, Lutz (author)
AstraZeneca, England
Schrauwen, Patrick (author)
Maastricht Univ Med Ctr, Netherlands
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 (creator_code:org_t)
NATURE PORTFOLIO, 2023
2023
English.
In: Nature Metabolism. - : NATURE PORTFOLIO. - 2522-5812. ; 5, s. 2086-2093
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Cotadutide is a dual glucagon-like peptide 1 and glucagon receptor agonist under development for the treatment of non-alcoholic steatohepatitis and type 2 diabetes mellitus (T2DM) and chronic kidney disease. Non-alcoholic steatohepatitis is a complex disease with no approved pharmacotherapies, arising from an underlying state of systemic metabolic dysfunction in association with T2DM and obesity. Cotadutide has been shown to improve glycaemic control, body weight, lipids, liver fat, inflammation and fibrosis. We conducted a two-part, randomized phase 2a trial in men and women with overweight or obesity diagnosed with T2DM to evaluate the efficacy and safety of cotadutide compared with placebo and liraglutide. The primary endpoints were change from baseline to day 28 of treatment in postprandial hepatic glycogen (part A) and to day 35 of treatment in fasting hepatic glycogen (part B) with cotadutide versus placebo. Secondary endpoints in part B were changes in fasting hepatic glycogen with cotadutide versus the mono glucagon-like peptide 1 receptor agonist, liraglutide, and change in hepatic fat fraction. The trial met its primary endpoint. We showed that cotadutide promotes greater reductions in liver glycogen and fat compared with placebo and liraglutide. Safety and tolerability findings with cotadutide were comparable to those of previous reports. Thus, this work provides evidence of additional benefits of cotadutide that could be attributed to glucagon receptor engagement. Our results suggest that cotadutide acts on the glucagon receptor in the human liver to promote glycogenolysis and improve the metabolic health of the liver. ClinicalTrials.gov registration: NCT03555994. In a two-part randomized phase 2a trial in men and women with overweight or obesity and type 2 diabetes mellitus, cotadutide promoted greater reductions in liver glycogen and fat than placebo and liraglutide.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

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