Status and phase
Conditions
Treatments
Study type
Funder types
Identifiers
About
The primary objective of this study is to demonstrate that KAI-9531 subcutaneous (SC) injection once weekly is superior to placebo on:
Enrollment
Sex
Ages
Volunteers
Inclusion and exclusion criteria
Key Inclusion Criteria:
Key Exclusion Criteria:
Note: Additional inclusion/exclusion criteria may apply, per protocol.
Primary purpose
Allocation
Interventional model
Masking
1,700 participants in 5 patient groups, including a placebo group
Loading...
Central trial contact
Kailera Therapeutics, Inc.
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal