New obesity drugs enter human trials in china
NCT ID NCT07017179
First seen Jun 25, 2026 · Last updated Jul 02, 2026 · Updated 2 times
Summary
This study tests two experimental drugs, AZD6234 and AZD9550, given as weekly injections to Chinese adults with obesity or overweight. About 871 participants will receive the drugs alone, together, or a placebo. The main goal is to check safety and how well the drugs work for weight loss.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- AZD6234 and AZD9550 (injectable drugs for weight loss)
- What this could lead to
- If successful, these drugs could offer a new option for weight management in people with obesity or overweight.
- What could go wrong
- This is an early phase 2 trial, so the drugs may not prove effective or safe enough. Side effects are possible, and results may not apply to non-Chinese populations.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
14 people
The number who actually took part.
- Started
-
May 2025
- Expected to finish
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Aug 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 55 years
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age 18 to 55 years. 2. BMI ≥ 27 kg/m2. 3. Stable body weight for 3 months prior to screening. 4. Male and female (Contraceptive use by participants or participant partners should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies). 5. Participants should refrain from blodd donation throughout the sub-study, including the follow-up period. 6. Negative pregnancy test at screening and randomisation for FOCBP and must not be breastfeeding. Exclusion Criteria: 1. Have received prescription medication or non-prescription medication for weight loss within the last 3 months prior to screening. 2. History of type 1 or type 2 diabetes mellitus or symptoms indicative of insulinopenia or poor glucose control. 3. Treatment with diabetes medication in past 3 months prior to screening. 4. HbA1c ≥ 6.5% (48 mmol/mol) at screening. 5. Gastroparesis (or similar) requiring treatment. 6. Significant inflammatory bowel disease or other severe disease or surgery affecting the upper GI tract. 7. Significant hepatic disease (except for non-alcoholic steatohepatitis or non-alcoholic fatty liver disease without portal hypertension or cirrhosis) and/or participants with any of the following results at screening: 1. AST ≥ 2.5 × ULN 2. ALT ≥ 2.5 × ULN 3. TBL ≥ 1.5 × ULN. 8. Prior history of cholecystectomy or untreated cholelithiasis. 9. History of acute or chronic pancreatitis or pancreatic amylase or lipase \> 2 × ULN at screening. 10. Severely uncontrolled hypertension defined as systolic BP ≥ 160 mmHg and/or diastolic BP ≥ 100 mmHg on the average of 2 seated measurements after being at rest for at least 5 minutes. 11. HR \< 50 bpm or \> 100 bpm after being at rest for 5 minutes. 12. Impaired renal function defined as eGFR ≤ 45 mL/minute/1.73 m2 at screening (GFR estimated according to CKD-EPI). 13. History of psychosis or bipolar disorder. 14. Severe vitamin D deficiency defined as a 25-OH vitamin D level \< 12 ng/mL. 15. Uncontrolled thyroid disease, defined as TSH \> ULN or \< LLN for the laboratory reference range, as judged by the PI at screening. Sub-study 2 only 16. Personal or family history (first-degree relative) of MTC or MEN2. 17. History of marijuana or THC use within 3 months before screening, or unwilling/unable to abstain from marijuana or THC use during the study. 18. Previous hospitalisation for any psychiatric reason. 19. PHQ-9 score ≥ 15 within the 2 years prior to screening or at screening.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Research Site
Jinan, 250001, China
-
Research Site
Nanjing, 210011, China
-
Research Site
Shanghai, 200032, China
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