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A Phase IIb Randomised, Double-blind, Placebo-controlled Study to Evaluate the Efficacy, Safety and Tolerability of Co-administration of AZD9550 and AZD6234 in Participants Living With Obesity or Overweight with Comorbidity

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-516176-15-00
Acronym
D8460C00004
Enrollment
40
Registered
2025-02-04
Start date
2025-02-24
Completion date
Unknown
Last updated
2025-12-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Investigating obesity or overweight condition correlated to many co-morbidities

Brief summary

Percent change in body weight from baseline after 36 weeks of treatment, Weight loss ≥ 5% from baseline after 36 weeks of treatment

Detailed description

Absolute change in body weight from baseline after 36 weeks of treatment, Percent and absolute change in body weight from baseline after 36 weeks of treatment, Weight loss ≥ 5% from baseline after 36 weeks of treatment, Weight loss ≥ 10% and ≥ 15% from baseline after 36 weeks of treatment, Prevalence, incidence and titres of ADAs to AZD9550 andAZD6234 in combination and as monotherapies after 36 weeks of treatment, To evaluate the safety and tolerability of AZD9550 and AZD6234 in combination compared with placebo and with monotherapy

Interventions

DRUGGLUCOSE
DRUGPlacebo for azd6234
DRUGPlacebo for azd9550
DRUGGLUCAGON
DRUGCALCIUM CARBONATE
DRUGONDANSETRON

Sponsors

AstraZeneca AB
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Percent change in body weight from baseline after 36 weeks of treatment, Weight loss ≥ 5% from baseline after 36 weeks of treatment

Secondary

MeasureTime frame
Absolute change in body weight from baseline after 36 weeks of treatment, Percent and absolute change in body weight from baseline after 36 weeks of treatment, Weight loss ≥ 5% from baseline after 36 weeks of treatment, Weight loss ≥ 10% and ≥ 15% from baseline after 36 weeks of treatment, Prevalence, incidence and titres of ADAs to AZD9550 andAZD6234 in combination and as monotherapies after 36 weeks of treatment, To evaluate the safety and tolerability of AZD9550 and AZD6234 in combination compared with placebo and with monotherapy

Countries

Germany

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026