Clinical trial

This is a Multi-centre, Multi-drug, Platform Study in Chinese Participants Living With Obesity / Overweight

Active, not recruiting · Phase 2 · 1 countries · Registry ID NCT07017179

Active, not recruitingPhase 2Interventional

What this study is about

This study is to assess the safety and tolerability, PK characterisation, efficacy, and immunogenicity of the study intervention, and it allows assessment of the monotherapy or combination therapy of AZD6234 and AZD9550 in different sub-studies.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age18 Years to 55 Years
SexAll
Healthy volunteersNot accepted
ConditionObesity/Overweight

Full registry criteria

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.

Treatments and study arms

AZD6234

Drug

Participants will receive a subcutaneous injection weekly

Placebo

Drug

Participants will receive a subcutaneous injection weekly.

AZD9550

Drug

Participants will receive a subcutaneous injection weekly

Plocebo

Drug

Participants will receive a subcutaneous injection weekly

AZD6234 in combination with AZD9550

Drug

Participants will receive a subcutaneous injection weekly

Placebo

Drug

Participants will receive a subcutaneous injection weekly

Primary outcomes

Numbers of participant with Adverse Events (AEs) and Serious adverse events (SAEs) (sub-study 1).From baseline to Day 141

To assess the safety and tolerability of repeated subcutaneous(SC) doses of AZD6234 compared to placebo.

Numbers of participant with Adverse Events (AEs) and Serious adverse events (SAEs) (sub-study 2).From baseline to Day 225

To assess the safety and tolerability of repeated SC doses of AZD9550 and AZD6234 in combination with AZD9550 compared to placebo.

Study locations

3 locations were listed when this page was built. The first 40 are shown.

Research Site🇨🇳 Jinan, China
Research Site🇨🇳 Nanjing, China
Research Site🇨🇳 Shanghai, China