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Document set current to 30 July 2026
Evidence synthesis · §3

Tirzepatide compared with semaglutide in type 2 diabetes — included and excluded studies

The included-studies table with extracted data, the exclusions with reasons, and the risk-of-bias judgements.

Document identifier
CEI-ES-029/3
Series
Evidence synthesis
Version
2.2
Published
26 Jan 2025
Last reviewed
26 Apr 2025
Next review
26 Oct 2026
Identifier
10.71829/cei.syn.29
Certainty
High
Cycle
2025 Q1
Review type
Intervention review
Search executed
05 Dec 2024

§3Included and excluded studies

Every study contributing to this review is listed below with the data extracted from it. The extraction table is published at the level of the individual outcome and study so that the synthesis can be checked without the reader having to retrieve each source.

§3.1Included studies

Table 4. Included studies with the characteristics extracted from each.

StudyDesignRandomisedDurationAnchor outcome as reportedYear
STRIDESemaglutideRandomised, double-blind, placebo-controlled79252 weeksEstimated treatment ratio 1.13 (95 % CI 1.06 to 1.21)2025
SURPASS-CVOTTirzepatideEvent-driven cardiovascular outcome trial13,299Median 4.5 yearsNon-inferior to dulaglutide on the primary composite. The Institute records that an active-controlled non-inferiority design cannot establish superiority over…2025
FLOWSemaglutideEvent-driven kidney outcome trial3,533Median 3.4 yearsHazard ratio 0.76 (95 % CI 0.66 to 0.88); annual eGFR slope difference 1.16 mL/min/1.73 m² per year2024
STEP-HFpEF-DMSemaglutideRandomised, double-blind, placebo-controlled61652 weeksDirectionally consistent with STEP-HFpEF with a smaller weight effect, as expected in a population with diabetes2024
SURMOUNT-2TirzepatideRandomised, double-blind, placebo-controlled93872 weeksMean change −14.7 % at 15 mg versus −3.2 % with placebo2023
SURPASS-5TirzepatideRandomised, double-blind, placebo-controlled47540 weeksReduction of 2.11 to 2.34 percentage points across doses versus 0.86 with placebo2022
STEP-2SemaglutideRandomised, double-blind, placebo-controlled1,21068 weeksMean change −9.6 % with semaglutide 2.4 mg versus −3.4 % with placebo; the effect is attenuated relative to STEP 1, which the Institute records as a consistent…2021
SURPASS-1TirzepatideRandomised, double-blind, placebo-controlled47840 weeksReduction of 1.87 to 2.07 percentage points across doses versus 0.04 with placebo2021
SURPASS-2TirzepatideRandomised, double-blind, active-controlled1,87940 weeksAll three tirzepatide doses were superior to semaglutide 1 mg; the largest difference was −0.45 percentage points at 15 mg2021
SURPASS-3TirzepatideRandomised, open-label, active-controlled1,44452 weeksSuperior glycaemic control with weight reduction rather than weight gain2021
SURPASS-4TirzepatideRandomised, open-label, active-controlled2,002Median 85 weeksSuperior glycaemic control; cardiovascular events were collected and adjudicated but the trial was not powered for a cardiovascular outcome2021
SUSTAIN-7SemaglutideRandomised, double-blind, active-controlled1,20140 weeksDifference −0.41 percentage points (95 % CI −0.57 to −0.25) for semaglutide 1.0 mg versus dulaglutide 1.5 mg2018
SUSTAIN-1SemaglutideRandomised, double-blind, placebo-controlled38830 weeksReduction of 1.5 percentage points with 1.0 mg versus 0.0 with placebo2017
SUSTAIN-6SemaglutideEvent-driven cardiovascular outcome trial3,297104 weeksHazard ratio 0.74 (95 % CI 0.58 to 0.95); designed to exclude harm rather than to establish benefit2016
14 included studies. Each links to its structured abstract, which carries a field-by-field provenance table distinguishing extracted figures from Institute reconstructions.

Contributing participants across studies reporting a randomised total: 31,552. Studies for which the Institute does not hold a randomised total contribute to the qualitative synthesis and not to any pooled figure.

§3.2Excluded at full text, with reasons

Table 5. Reports excluded at full text, by reason. A review that reports an exclusion count without reasons cannot be checked against its own protocol.

Reason for exclusionReports
Not a randomised comparison6
Population outside the review question7
Intervention outside the review question6
Comparator not eligible5
No eligible outcome reported4
Duplicate report of an included study3
Conference abstract without extractable data4
Retracted or subject to an expression of concern4
28 reports excluded at full text in total.

§3.3Risk of bias across included studies

Table 6. Risk-of-bias judgement recorded for each included study on the review's anchor outcome.

StudyRisk of biasInconsistencyIndirectnessImprecisionPublication bias
STRIDELowSomeLowLowLow
SURPASS-CVOTLowLowLowSomeLow
FLOWLowLowLowLowLow
STEP-HFpEF-DMLowSomeLowLowLow
SURMOUNT-2LowLowLowLowLow
SURPASS-5LowLowLowLowLow
STEP-2LowLowLowLowLow
SURPASS-1LowLowLowLowLow
SURPASS-2LowLowLowLowLow
SURPASS-3LowLowLowLowLow
SURPASS-4LowLowLowLowLow
SUSTAIN-7LowLowLowLowLow
SUSTAIN-1LowLowLowLowLow
SUSTAIN-6LowLowLowLowLow
Judgements are the Institute's own and are recorded per outcome. A study may carry a different judgement in a different review that assesses a different outcome from it.

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. Frías JP, Davies MJ, Rosenstock J, Pérez Manghi FC, Fernández Landó L, Bergman BK, Liu B, Cui X, Brown K. Tirzepatide versus semaglutide once weekly in patients with type 2 diabetes. New England Journal of Medicine 2021;385(6):503–515. doi:10.1056/NEJMoa2107519 · PMID 34170647

Identifiers are reproduced only where the Institute holds them. Where a digital object identifier or PubMed identifier is not shown, the Institute has recorded the journal and year and has not constructed an identifier.

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