Abstract | AIMS: METHODS: RESULTS: Overall, 7056 individuals were included in the analysis, and there were 67 primary endpoint events during 7478 person-years of follow-up (40 vs 27 events in the intervention vs control groups, respectively). The odds ratio for the composite endpoint among people randomized to taspoglutide was 0.94 (95% confidence interval 0.57-1.56), which was robust across multiple subgroups. Longer-term data were not available as the development of taspoglutide was stopped because of gastrointestinal intolerance and serious hypersensitivity reactions. CONCLUSIONS: The available data suggest that short-term, once-weekly administration of taspoglutide was not associated with an excess risk of CVD, and provide insights relevant to the development of other novel once-weekly incretin mimetics.
|
Authors | S R K Seshasai, R L Bennett, J R Petrie, M Bengus, S Ekman, M Dixon, M Herz, J B Buse, K K Ray |
Journal | Diabetes, obesity & metabolism
(Diabetes Obes Metab)
Vol. 17
Issue 5
Pg. 505-10
(May 2015)
ISSN: 1463-1326 [Electronic] England |
PMID | 25656522
(Publication Type: Journal Article, Meta-Analysis, Research Support, Non-U.S. Gov't, Review)
|
Copyright | © 2015 John Wiley & Sons Ltd. |
Chemical References |
- Glucagon-Like Peptide-1 Receptor
- Peptides
- taspoglutide
|
Topics |
- Cardiovascular Diseases
(etiology)
- Clinical Trials, Phase III as Topic
- Diabetes Mellitus, Type 2
(drug therapy)
- Drug Administration Schedule
- Female
- Glucagon-Like Peptide-1 Receptor
(administration & dosage, agonists)
- Humans
- Male
- Middle Aged
- Peptides
(administration & dosage, adverse effects)
- Randomized Controlled Trials as Topic
- Treatment Outcome
|