Poster Presentation Australian and New Zealand Obesity Society Annual Scientific Conference 2024

Patient experiences with tirzepatide in SURMOUNT-4 (#239)

Irina Jouravskaya 1 , Chisom Kanu 1 , Jiat Ling Poon 1 , Donna Mojdami 1 , Elizabeth Collins 1 , Danielle Burns 1 , Helen Kitchen 1 , Chloe Carmichael 1 , Kevin Lee 1 , Roger Chen 2
  1. Novo Nordisk, Søborg, Denmark
  2. Concord Repatriation General Hospital, Concord, NSW, Australia

Introduction & Objective:  Exit interviews were conducted with participants of the SURMOUNT-4 clinical trial to understand their experiences of weight loss and maintenance of weight loss with tirzepatide.

Methods: SURMOUNT-4 was a phase 3 clinical trial of tirzepatide in adults living with obesity or overweight with at least one weight-related comorbidity. Participants received 36 weeks of maximum tolerated dose of tirzepatide in an open-label, lead-in treatment period, following which they were randomized to continue on tirzepatide or switch to placebo for a double-blind maintenance treatment period of 52 weeks. After completion of a 4-week safety follow-up period, cross-sectional qualitative exit interviews were conducted with 86 US-based participants.

Results:  On average, exit interview participants lost 25kg during the open-label period. Most (n=84) described at least one physiological improvement during this period, such as increased energy (n=53). Participants (n=73) also reported positive impacts on their physical functioning including improved walking ability (n=36) and increased activity levels (n=30). Other improvements during this period pertained to emotional well-being (n=78), social life and relationships (n=64), activities of daily living (n=40), ability to work (n=15), and participation in hobbies (n=7). Participants were generally positive about the efficacy of tirzepatide (n=59) and how it reduced their appetite (n=35) and/or cravings (n=19). The most common aspect of treatment disliked by participants was gastrointestinal side effects (n=34). 

During the maintenance period, all participants on tirzepatide reported one or more additional improvements, or sustenance of the improvements achieved pre-randomization. In contrast, nearly all participants on placebo reported some loss of improvements experienced pre-randomization.

Conclusion: Participants were largely positive about tirzepatide’s effect on weight loss and the subsequent positive impacts on their broader well-being.