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Completed Phase 2 Interventional

Aleniglipron Phase 2 in Type 2 Diabetes Mellitus

ClinicalTrials.gov ID: NCT07400588

Public ClinicalTrials.gov record NCT07400588. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 8, 2026, 10:42 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Randomized, Double-blind, Placebo-controlled, Study of the Safety and Tolerability of Aleniglipron in Adult Participants With Type 2 Diabetes Mellitus Living With Obesity or Overweight

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to assess the safety and tolerability of aleniglipron at doses up to 180 mg once daily (QD) in participants with T2DM who are living with obesity (body mass index \[BMI\] ≥ 30 kg/m2) or overweight (BMI ≥ 27 kg/m2).

Study identification

NCT ID
NCT07400588
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
58 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 79 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 1, 2025 (Actual)
Primary completion
Sep 18, 2026 (Actual)
Completion
Sep 18, 2026 (Actual)
Last update posted
Oct 21, 2026

2025 – 2026

United States locations

U.S. sites
16
U.S. states
7
U.S. cities
14
Facility City State ZIP Site status
Research Site Anniston Alabama 36207 —
Research Site Lake Forest California 92630 —
Research Site Lomita California 90717 —
Research Site Hazelwood Missouri 63042 —
Research Site Columbus Ohio 43212 —
Research Site Moncks Corner South Carolina 29461 —
Research Site Chattanooga Tennessee 37421 —
Research Site Knoxville Tennessee 37909 —
Research Site Austin Texas 78704 —
Research Site DeSoto Texas 75115 —
Research Site Houston Texas 77079 —
Research Site Mesquite Texas 75149 —
Research Site San Antonio Texas 78215 —
Research Site San Antonio Texas 78229 —
Research Site San Antonio Texas 78240 —
Research Site Tomball Texas 77375 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07400588, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 21, 2026 · Synced Nov 8, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07400588 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →