Independent · non-commercial · publishes on a quarterly cycle|Current cycle 2026 Q3
Compound Evidence InstituteEvidence synthesis · established 2023Graded assessments of compounds, trials, methods and supply
Document set current to 30 July 2026
Trial abstract · §3

DREAMS-1 — results

Primary endpoint, absolute and relative effect where derivable, and harms as reported.

Document identifier
CEI-TR-0136/3
Series
Trial abstract
Version
3.3
Published
14 Jan 2024
Last reviewed
14 Mar 2025
Next review
14 Mar 2027
Identifier
10.71829/cei.trial.136
Certainty
Moderate
Cycle
2024 Q1
Phase
Phase 3
Status
Reported

§3Results

§3.1Primary endpoint

Table 3. Primary endpoint as reported.

EndpointResult as reportedCertainty
Change in glycated haemoglobin from baseline to week 24 as monotherapy in Chinese adults with type 2 diabetesA reduction of approximately 1.6 percentage points at 6 mg versus 0.1 with placeboModerate
Reproduced from the published report. Where the report states a confidence interval the Institute reproduces it; where it does not, none is constructed.

§3.2Endpoint hierarchy

§3.3Harms as reported

Table 5. Adverse events for Mazdutide from the safety tables the Institute holds for this compound. Where a row names a different trial as its source, the figure is from that trial and not from this one.

EventActive, %Comparator, %Source trial
Nausea32.08.0Phase 3 obesity (6 mg)
Diarrhoea22.09.0Phase 3 obesity
Vomiting16.02.0Phase 3 obesity
Increased heart rateReported; attributed to the glucagon arm
Discontinuation for adverse events5.02.0Phase 3 obesity
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