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
Document series

Trial abstracts — page 9

700 structured trial abstracts. Each is one document in five parts: abstract, design and population, results, certainty assessment and citing documents.

Showing 0 records on this page

Trial records

700 documents · page 9 of 30

Table 1. Trial records on this page. The table sorts on any column and filters on the controls above; both operate on the records shown on this page only.

RecordCompoundPhaseStatusDesignRandomisedYearCertainty
SURPASS-CVOT-DDIprogramme recordTirzepatidePhase 1ReportedRandomised crossover2025Very low
SURPASS-CVOT-PKprogramme recordTirzepatidePhase 1ReportedPhase 1 ascending dose2025Very low
SURPASS-CVOT-RENAL-IMPprogramme recordTirzepatidePhase 1ReportedPhase 1 ascending dose2025Very low
DREAMS-2-PKprogramme recordMazdutidePhase 1ReportedPhase 1 ascending dose2024Very low
DREAMS-2-RENAL-IMPprogramme recordMazdutidePhase 1ReportedPhase 1 ascending dose2024Very low
FLOW-HEPATIC-IMPprogramme recordSemaglutidePhase 1ReportedPhase 1 ascending dose2024Very low
FLOW-PKprogramme recordSemaglutidePhase 1ReportedPhase 1 ascending dose2024Very low
FLOW-RENAL-IMPprogramme recordSemaglutidePhase 1ReportedPhase 1 ascending dose2024Very low
MARITIDE-PH2-OBESITY-HEPATIC-IMPprogramme recordMaridebart cafraglutidePhase 1ReportedPhase 1 ascending dose2024Very low
MARITIDE-PH2-T2D-BODY-COMPprogramme recordMaridebart cafraglutidePhase 2ReportedRandomised, double-blind, placebo-controlled2024Very low
MARITIDE-PH2-T2D-REGIONAL-CNprogramme recordMaridebart cafraglutidePhase 3ReportedRandomised, double-blind, placebo-controlled2024Very low
MARITIDE-PH2-T2D-REGIONAL-JPprogramme recordMaridebart cafraglutidePhase 3ReportedRandomised, double-blind, placebo-controlled2024Very low
PETRE-PH1B-ADHERENCEprogramme recordPetrelintidePhase 1ReportedObservational2024Very low
PETRE-PH1B-BIOMARKERprogramme recordPetrelintidePhase 1ReportedRandomised, double-blind, placebo-controlled2024Very low
PETRE-PH1B-ELDERLYprogramme recordPetrelintidePhase 1ReportedRandomised, double-blind, placebo-controlled2024Very low
PETRE-PH1B-PKprogramme recordPetrelintidePhase 1ReportedPhase 1 ascending dose2024Very low
REIMAGINE-1-DDIprogramme recordAmycretinPhase 1ReportedRandomised crossover2024Very low
REIMAGINE-1-PKprogramme recordAmycretinPhase 1ReportedPhase 1 ascending dose2024Very low
REIMAGINE-1-RENAL-IMPprogramme recordAmycretinPhase 1ReportedPhase 1 ascending dose2024Very low
STEP-HFpEF-DM-BODY-COMPprogramme recordSemaglutidePhase 3ReportedRandomised, double-blind, placebo-controlled2024Very low
SUMMIT-ADHERENCEprogramme recordTirzepatidePhase 3ReportedObservational2024Very low
SUMMIT-BIOMARKERprogramme recordTirzepatidePhase 3ReportedRandomised, double-blind, placebo-controlled2024Very low
SUMMIT-ELDERLYprogramme recordTirzepatidePhase 3ReportedRandomised, double-blind, placebo-controlled2024Very low
SUMMIT-OLEprogramme recordTirzepatidePhase 3ReportedSingle-arm open-label2024Very low

page 9 of 30

Nothing published by the Institute is medical advice, a diagnosis, a prescription, a treatment recommendation or a purchasing recommendation. Compounds supplied for research use are not approved for human or veterinary use in any jurisdiction, and a favourable analytical assessment of a supplier is not a statement that any product is safe or effective. The Institute publishes certainty ratings and never recommendations. No telephone number, messaging handle or ordering channel appears anywhere on this site.