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Document set current to 30 July 2026
Evidence synthesis · Safety review

Semaglutide in heart failure with preserved ejection fraction and obesity: tolerability and discontinuation

In the population defined for heart failure with preserved ejection fraction and obesity, what is the incidence of adverse events leading to discontinuation with Semaglutide compared with its comparator?

Document identifier
CEI-ES-113
Series
Evidence synthesis
Version
1.2
Published
23 May 2025
Last reviewed
23 Jan 2026
Next review
23 Jul 2027
Identifier
10.71829/cei.syn.113
Certainty
Moderate
Cycle
2025 Q2
Review type
Safety review
Search executed
05 Feb 2025

Templated review frame. This review question was generated by crossing an indication with a compound for which contributing trials exist. Its prose frame is templated and is shared with other questions of the same shape. Its included studies, its summary of findings and its certainty rating are computed from the underlying records and are not templated. The Institute publishes these questions because the alternative is to leave a question the document set can answer unanswered, and it labels them because the alternative is to present a templated frame as an authored one.

§1Abstract

§1.1Review question

In the population defined for heart failure with preserved ejection fraction and obesity, what is the incidence of adverse events leading to discontinuation with Semaglutide compared with its comparator?

§1.2PICO frame

Table 1. The registered PICO frame. Any change made after protocol registration is recorded in the amendment log at §5 and is identified there as post hoc.

ElementAs registered
PopulationSymptomatic heart failure with a left ventricular ejection fraction of 50 % or above, occurring with obesity as a dominant phenotypic driver.
InterventionSemaglutide administered as subcutaneous once weekly; oral once daily with a permeation enhancer (see separate monograph).
ComparatorThe comparator used in each contributing trial, reported per trial rather than pooled across comparator types.
OutcomesAnchor outcome for this indication: Change in Kansas City Cardiomyopathy Questionnaire clinical summary score. Additional outcomes: Change in six-minute walk distance; Composite of cardiovascular death and worsening heart-failure events; Change in NT-proBNP.

§1.3Method in brief

A review of harms, in which the absence of an event in a trial of conventional size is treated as uninformative rather than as reassurance. The protocol was registered with the Institute's secretariat before the search was executed. The search was run on 5 February 2025 across 8 sources and is reproduced in full at §2. Screening, extraction and certainty assessment were performed independently by two members of the secretariat with disagreement resolved by a third.[1,2]

§1.4Conclusion

Moderate certainty evidence from 2 contributing trials bears on tolerability. Discontinuation for adverse events is reported in the summary-of-findings table alongside the efficacy outcomes rather than in an annex, because a trial reporting a given effect with high discontinuation is reporting a materially different result from one reporting the same effect with high persistence.

The conclusion rests on 2 contributing studies, listed with their extracted data at §3 and summarised outcome by outcome at §4.

§1.5Limitations

References cited on this page

References are numbered in order of first citation in this document. Each superscript in the text links to its entry below.

  1. Wilding JPH, Batterham RL, Calanna S, Davies M, Van Gaal LF, Lingvay I, McGowan BM, Rosenstock J, Tran MTD, Wadden TA, Wharton S, Yokote K, Zeuthen N, Kushner RF. Once-weekly semaglutide in adults with overweight or obesity. New England Journal of Medicine 2021;384(11):989–1002. doi:10.1056/NEJMoa2032183 · PMID 33567185
  2. Davies M, Færch L, Jeppesen OK, Pakseresht A, Pedersen SD, Perreault L, Rosenstock J, Shimomura I, Viljoen A, Wadden TA, Lingvay I. Semaglutide 2·4 mg once a week in adults with overweight or obesity, and type 2 diabetes (STEP 2): a randomised, double-blind, double-dummy, placebo-controlled, phase 3 trial. The Lancet 2021;397(10278):971–984. doi:10.1016/S0140-6736(21)00213-0 · PMID 33667417

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