LivingGLP1
Study S003380

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 Co-morbidity (ASCEND)

Registration

Registration
NCT06862791
Acronym
ASCEND
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
377
Start
2025-02-18
Primary completion
2026-05-11
Lead sponsor
AstraZeneca
Conditions
Obesity or Overweight
Interventions
DRUG:AZD9550; DRUG:AZD6234; DRUG:Placebo comparator
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
REGISTRY:2024-516176-15-00

Registered primary outcomes

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

Linked records (0)

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