Obesity

Semaglutide 2.4 mg in French people living with Class 3 obesity and comorbidities: Baseline characteristics and real-world safety data

Diabetes MetabPublished Descriptive real-world cohort study

Authors' conclusion

- The high number of treatment prescriptions in a short period highlights the high unmet medical need. No new safety concerns were identified in this population with severe obesity treated in a real-world setting.

Study context

Population
French patients with body mass index (BMI) ≥40 kg/m² and ≥1 treated weight-related comorbidity (hypertension, dyslipidemia, obstructive sleep apnea, CVD) receiving semaglutide 2.4 mg; age 18 to 81 years
Participants
478 vs 8,568
Exposure
TUA vs EAP
  • TUAn = 478
  • EAPn = 8,568
Outcome
Baseline BMI
Follow-up
Baseline
Methodological detailsTemporary Utilization Authorization and Early Access Program cohorts, descriptive statistics only
  • Temporary Utilization Authorization and Early Access Program cohorts
  • Descriptive statistics only

Main finding

As reported in the abstract

Treatment requests sent by sites specialized in obesity management
5,797 (62.8%)

Observational data: associations, not effects.

Further findings

Number of WRC (EAP) · baseline

1 WRC
57.4%
2 WRC
26.5%
3 WRC
12.3%
4 WRC
3.7%

Other comorbidities · baseline

T2D
15.5%
Depression
18.1%
Osteoarthritis
15.4%

Safety

OutcomeTUAEAP
Treatment discontinuationTUA count: discontinued due to AEs3 events2.9%
Median time to discontinuation— not stated in the abstract2.8 months (IQR: 1.2-5.1)
Due to AEs— not stated in the abstract47.0%

— not stated in the abstract

Pancreatitis

Pancreatitis cases overall
7

Original publication

Semaglutide 2.4 mg in French people living with Class 3 obesity and comorbidities: Baseline characteristics and real-world safety data. Diabetes Metab. Published 17 February 2025. doi:10.1016/j.diabet.2025.101625

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