Safety, tolerability and sustained weight loss over 2 years with the once-daily human GLP-1 analog, liraglutide
University of Copenhagen · Hospital Universitario de La Princesa · +11 more institutions
Abstract
Having demonstrated short-term weight loss with liraglutide in this group of obese adults, we now evaluate safety/tolerability (primary outcome) and long-term efficacy for sustaining weight loss (secondary outcome) over 2 years.
A randomized, double-blind, placebo-controlled 20-week study with 2-year extension (sponsor unblinded at 20 weeks, participants/investigators at 1 year) in 19 European clinical research centers. SUBJECTS: A total of 564 adults (n=90-98 per group; body mass index 30-40 kg m(-2)) enrolled, 398 entered the extension and 268 completed the 2-year trial. Participants received diet (500 kcal deficit per day) and exercise counseling during 2-week run-in, before being randomly assigned (with a telephone or web-based system) to once-daily subcutaneous liraglutide (1.2, 1.8, 2.4 or 3.0 mg, n=90-95), placebo (n=98) or open-label orlistat (120 mg × 3, n=95). After 1 year, liraglutide/placebo recipients switched to liraglutide 2.4 mg, then 3.0 mg (based on 20-week and 1-year results, respectively). The trial ran from January 2007-April 2009 and is registered with Clinicaltrials.gov, number NCT00480909.
Citation impact
- FWCI
- 28.40
- Percentile
- 100%
- References
- 36
Authors
13- OBon behalf of the NN8022-1807 InvestigatorsCorresponding
University of Copenhagen
- AAArne Astrup
University of Copenhagen, Hospital Universitario de La Princesa
- RCRaffaele Carraro
Hospital Universitario de La Princesa, University College London
- NFNick Finer
Novo Nordisk (Denmark), University College London
- AEA E Harper
Novo Nordisk (Denmark), Institute of Endocrinology
Topics & keywords
- Liraglutide
- Tolerability
- Weight loss
- Medicine
- Internal medicine
- Endocrinology
- Pharmacology
- Obesity
- Good health and well-being