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NCT05318326

A Randomized, Double-blind, Placebo-controlled, Multicenter Clinical Trial to Evaluate the Clinical Efficacy and Safety of Yogliptin Tablets

Status unknown Phase 3 Last updated 20 April 2022
What this trial tests

Phase 3 trial testing placebo group in Type 2 Diabetes in 450 participants. Status unknown.

Timeline
1 January 2022
Primary endpoint
31 December 2024
31 December 2024

Quick facts

Lead sponsorChengdu Easton Biopharmaceuticals Co,Ltd
PhasePhase 3
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment450
Start date1 January 2022
Primary completion31 December 2024
Estimated completion31 December 2024
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Chengdu Easton Biopharmaceuticals Co,Ltd — full company profile →

Who can join

Adults 18 to 75, any sex, with Type 2 Diabetes. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to assess the efficacy of Yogliptin (as monotherapy) compared with placebo after 24 weeks, and the safety (up to 52 weeks) of Yogliptin in Chinese patients with Type 2 diabetes who are insufficient glycaemic control with diet and exercise.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Signaling pathways in obesity: mechanisms and therapeutic interventions.
    Wen X, Zhang B, Wu B, Xiao H, et al · · 2022 · cited 245× · PMID 36031641 · DOI 10.1038/s41392-022-01149-x

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Other recruiting trials for Type 2 Diabetes

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05318326.

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