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NCT06988553CompletedPhase 1

A Phase Ib Study of AZD5004 in Chinese Participants With Overweight/Obesity With or Without Type 2 Diabetes Mellitus

A Phase Ib, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of AZD5004 in Chinese Participants With Overweight/Obesity With or Without Type 2 Diabetes Mellitus

Source: ClinicalTrials.gov · Last updated 23 Dec 2025

Brief summary (registry, in English)

The purpose of this study is to evaluate the safety, tolerability, and PK of AZD5004 compared with placebo in Chinese participants with overweight/obesity with or without T2DM.

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
45 (actual)
First submitted
16 May 2025
Start date
17 Jun 2025
Primary completion date
28 Nov 2025
Lead sponsor
Eccogene
NCT number
NCT06988553

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 45
  • From 17 Jun 2025 to the primary completion date, 28 Nov 2025
  • 6 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of, or any existing condition that influence the participant's ability to participate or affect the interpretation of the results of the study.
  • Significant hepatic disease.
  • History of acute pancreatitis and chronic pancreatitis, gallstones.
  • Uncontrolled thyroid disease.

Other

  • Known clinically significant gastric emptying abnormality.
  • Abnormal renal function.

Who the study is looking for

  • Aged 18 to 74 years inclusive at the time of signing the informed consent.
  • Stable self-reported body weight for 3 months prior to Screening.
  • \- 27 kg/m2 ≤ BMI ≤ 35 kg/m2 and weigh at least 60 kg at Screening.
  • Diagnosed with T2DM for at least 6 months prior to signing the informed consent.
  • HbA1c value at Screening of ≥ 7.0% and ≤ 10.5%
  • BMI of ≥ 24 kg/m2 at the Screening Visit.

Age in the registry: 18 years to 74 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (6)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
West China Hospital,Sichuan University
Coordinator of this site? Confirm its status
ChengduChinaUnknown status
The Fourth Affiliated Hospital of Harbin Medical University
Coordinator of this site? Confirm its status
Ha’erbinChinaUnknown status
The Second People's Hospital of Hefei
Coordinator of this site? Confirm its status
HefeiChinaUnknown status
Jinan Central Hospital
Coordinator of this site? Confirm its status
JinanChinaUnknown status
Shanghai Pudong New District People's Hospital
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status
General Hospital of Tianjin Medical University
Coordinator of this site? Confirm its status
TianjinChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.