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American Heart Association

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Final ID: MDP453

Once Weekly Utreglutide (GL0034), a Glucagon-like Peptide-1 Receptor Agonist, at 4 × 450 µg Doses Reduces Blood Pressure, Lipids, and Body Weight in Post-menopausal Females: A Phase I Study

Abstract Body (Do not enter title and authors here): Background
Utreglutide (GL0034), a novel, once weekly glucagon-like peptide-1 receptor agonist (GLP-1RA), previously demonstrated significant reductions in body weight (BW) after a single dose ascending study in individuals with obesity. BW reductions after pharmacological treatment of obesity with GLP-1RA is associated with blood pressure (BP) lowering effects.
Aim
This phase I study assessed the safety, tolerability, and cardio-metabolic effects of utreglutide after multiple ascending doses in post-menopausal female volunteers with overweight and obesity.
Methods
In this randomized, double-blind, placebo-controlled study 12 post-menopausal female volunteers with overweight/obesity, aged 18 to 65 years old with a body mass index (BMI) ≥26 kg/m2 were randomized (9:3) to subcutaneous utreglutide fixed doses (4 × 450 µg); or placebo once weekly for four weeks. Safety, tolerability, and key cardio-metabolic parameters were assessed. Biomarker measurements included oral glucose tolerance test (OGTT) insulin and glucose area under the curve (AUC), systolic- and diastolic BP, lipid profile (triglycerides (TG), total cholesterol (TC), low density lipoprotein (LDL), and non-high-density lipoprotein (non-HDL), creatinine, potassium, BW and leptin.
Results
Utreglutide was generally well tolerated and related adverse effects were mainly gastrointestinal with dose-dependent nausea, vomiting and decreased appetite. Reductions in OGTT AUCs of insulin (p<0.05) and glucose (p<0.01) were noted on Day 23 after four weeks treatment with Utreglutide. This was accompanied by a decrease (p<0.001) in mean systolic and diastolic BP on Day 23 from baseline (BL). On Day 23, significant reductions in TC (p<0.01), LDL (p<0.05) and non-HDL (p<0.05) were observed. BW reduction versus BL (p<0.001) was 2.0 kg and 1.8 kg respectively on Day 29 and End of Study (EoS). Leptin levels significantly reduced from BL on Day 23 (p<0.01) and EoS (p<0.001). No significant changes were observed for TG, creatinine and potassium (Table).
Conclusions
Once weekly utreglutide dosing for four weeks at a dose of 450 µg in post-menopausal females with overweight and obesity, demonstrated clinically relevant reductions of systolic and diastolic BP. This was associated with improved performance of OGTT AUC of insulin and glucose, lipids, BW and leptin with an overall good tolerability and with potential to demonstrate cardio-metabolic benefits.
  • Thennati, Rajamannar  ( High Impact Innovations – Sustainable Health Solutions (HISHS), Sun Pharmaceutical Industries Ltd , Vadodara, Gujarat , Gujarat , India )
  • Vilsboll, Tina  ( Clinical Research, Steno Diabetes Center Copenhagen, Herlev, University of Copenhagen, , Copenhagen , Denmark )
  • Burade, Vinod  ( High Impact Innovations – Sustainable Health Solutions (HISHS), Sun Pharmaceutical Industries Ltd , Vadodara, Gujarat , Gujarat , India )
  • Natarajan, Muthukumaran  ( High Impact Innovations – Sustainable Health Solutions (HISHS), Sun Pharmaceutical Industries Ltd , Vadodara, Gujarat , Gujarat , India )
  • Shahi, Pradeep  ( High Impact Innovations – Sustainable Health Solutions (HISHS), Sun Pharmaceutical Industries Ltd , Vadodara, Gujarat , Gujarat , India )
  • Nagaraja, Ravishankara  ( High Impact Innovations – Sustainable Health Solutions (HISHS), Sun Pharmaceutical Industries Ltd , Vadodara, Gujarat , Gujarat , India )
  • Agrawal, Sudeep  ( High Impact Innovations – Sustainable Health Solutions (HISHS), Sun Pharmaceutical Industries Ltd , Vadodara, Gujarat , Gujarat , India )
  • Duvauchelle, Thierry  ( Phaster1, Le Plessis-Trévise , Paris , France )
  • Pratley, Richard  ( AdventHealth Orlando , Orlando , Florida , United States )
  • Thorens, Bernard  ( Center for Integrative Genomics, University of Lausanne , Lausanne , Switzerland )
  • Author Disclosures:
    Rajamannar Thennati: DO NOT have relevant financial relationships | Tina Vilsboll: No Answer | Vinod Burade: DO have relevant financial relationships ; Employee:Sun Pharmaceutical Industries Limited:Active (exists now) | Muthukumaran Natarajan: No Answer | Pradeep Shahi: No Answer | Ravishankara Nagaraja: DO NOT have relevant financial relationships | Sudeep Agrawal: No Answer | Thierry Duvauchelle: No Answer | Richard Pratley: DO have relevant financial relationships ; Consultant:AbbVie Inc.; Bayer AG; Pfizer:Active (exists now) ; Consultant:Intas Pharmaceuticals Inc.:Past (completed) ; Speaker:Lilly USA LLC; Novo Nordisk:Active (exists now) ; Consultant:Genprex; Getz Pharma; Sun Pharmaceuticals:Past (completed) ; Consultant:Gasherbrum Bio, Inc.; Scholar Rock Inc.:Active (exists now) ; Researcher:Fractyl; Novo Nordisk; Sanofi:Active (exists now) ; Consultant:Endogenex Inc.; Novo Nordisk:Active (exists now) ; Consultant:Rivus Pharmaceuticals Inc.:Active (exists now) ; Researcher:Dompe; Endogenex Inc.:Active (exists now) ; Consultant:Corcept Therapeutics Incorporated:Active (exists now) ; Researcher:Carmot Therapeutics:Active (exists now) ; Researcher:Biomea Fusion; Lilly; Scholar Rock Inc.:Active (exists now) ; Consultant:Bayer HealthCare Pharmaceuticals Inc.:Active (exists now) ; Consultant:Eli Lilly; Lilly USA LLC:Active (exists now) ; Consultant:AstraZeneca Pharmaceuticals LP:Active (exists now) | Bernard Thorens: DO have relevant financial relationships ; Consultant:Sun Pharma:Active (exists now)
Meeting Info:

Scientific Sessions 2024

2024

Chicago, Illinois

Session Info:

Prevention Can’t Weight: Emerging Therapeutic Strategies for Obesity and CVD

Saturday, 11/16/2024 , 12:50PM - 02:15PM

Moderated Digital Poster Session

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