LivingGLP1
Study S002332

A Phase 1, Randomised, Double-blind, Placebo-controlled, Single and Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of XW003 Injection in Healthy Adult Participants

Registration

Registration
NCT04389775
Acronym
XW003
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
64
Start
2020-03-29
Primary completion
2021-09-29
Lead sponsor
Sciwind Biosciences APAC CO Pty. Ltd.
Conditions
Type 2 Diabetes Mellitus; Obesity; Nonalcoholic Steatohepatitis
Interventions
DRUG:Cohort A; DRUG:Placebo A; DRUG:Cohort B; DRUG:Placebo B
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
REGISTRY:ACTRN12620000344998

Registered primary outcomes

  • Number of treatment emergent adverse events (TEAEs) [From administration of XW003 on Day 1 to the last follow-up visit]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0009494Discovery of ecnoglutide - A novel, long-acting, cAMP-biased glucagon-like peptide-1 (GLP-1) analog.
Guo W, Molecular metabolism
2023Randomized trialPMID 37364710DOIcites ClinicalTrials.gov:NCT04389775; registry reference DERIVED:37364710