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

ACHIEVE-2 — structured trial abstract

ACHIEVE-2 — Orforglipron in type 2 diabetes: randomised, double-blind, active-controlled

Document identifier
CEI-TR-0048
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

§1Structured abstract

§1.1Objective

To evaluate Orforglipron in type 2 diabetes mellitus, against the comparator specified in §2, with the primary endpoint stated below.

§1.2Design

Design
Randomised, double-blind, active-controlled, parallel-group
Masking
Double-blind (participant and investigator)
Phase
Phase 3
Randomised participants
not recorded by the Institute
Duration of the primary analysis period
52 weeks
Sponsor class
Manufacturer-sponsored
Registry identifier
not reproduced — see the note in §1.5

§1.3Primary endpoint

Change in glycated haemoglobin from baseline, orforglipron versus an active comparator

§1.4Principal result

The Institute holds no reported primary result for this trial. Where a result exists and the Institute has not obtained it, the record says so rather than leaving the field blank.

§1.5Provenance of this abstract

Table 1. Field-by-field provenance. The Institute records which fields are extracted from a source and which are its own reconstruction, so that a reader can tell the two apart without leaving the page.

FieldProvenanceNote
Design, phase, duration, primary endpointExtractedReproduced from the published report or the registry record.
Randomised participantsNot heldNot recorded by the Institute. The field is left empty rather than estimated.
Principal resultNot heldNo result is reproduced.
Centres, countries and baseline characteristicsReconstructedDerived by the Institute from the design class and the randomised total. Presented in §2 as an illustrative operational profile and marked as such. These figures are not published characteristics of this trial.
Certainty assessmentInstitute judgementThe Institute’s own domain-by-domain assessment, with reasoning recorded against each domain in §4.
Registry identifierNot heldThe Institute does not reproduce a registry identifier it has not verified and never constructs one. Documents are referenced by the Institute’s own identifier.
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