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 · §2

ACHIEVE-2 — design and population

Design, allocation, arms and the population enrolled.

Document identifier
CEI-TR-0048/2
Series
Trial abstract
Version
1.3
Published
18 Feb 2025
Last reviewed
18 Mar 2026
Next review
18 Mar 2028
Identifier
10.71829/cei.trial.48
Certainty
Not rated
Cycle
2025 Q1
Phase
Phase 3
Status
Reported

§2Design and population

§2.1Design and allocation

Design class
Randomised, double-blind, active-controlled, parallel-group
Masking
Double-blind (participant and investigator)
Arms
2
Allocation
Randomised between the intervention and its comparator
Endpoint adjudication
Not applicable to the primary endpoint of this design
Data monitoring
As specified in the protocol

§2.2Arms

Table 2. Randomised arms. Illustrative: arm-level allocations are reconstructed by the Institute from the design class and the randomised total where the published report does not state them.

ArmAllocatedShareDescription
OrforglipronIntervention at the dose reached after titration
Active comparatorComparator agent at the dose specified in the protocol
The randomised total is not recorded by the Institute and arm-level figures are therefore not presented.

§2.3Population

Indication. Type 2 diabetes mellitus

A disorder of glucose regulation characterised by insulin resistance with relative insulin deficiency, diagnosed by glycated haemoglobin, fasting plasma glucose or oral glucose tolerance criteria.

Geographic footprint. Poland · Republic of Korea · Australia · China.

§2.4Eligibility as the Institute reads it

  • Included. A disorder of glucose regulation characterised by insulin resistance with relative insulin deficiency, diagnosed by glycated haemoglobin, fasting plasma glucose or oral glucose tolerance criteria.
  • Excluded. Participants for whom the intervention is contraindicated, including not established — investigational. Exclusion criteria narrow the population to which the estimate applies and are the principal source of indirectness where a trial estimate is applied to ordinary practice.
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