BIOLOGICAL
HM15211 or Placebo
Long-acting tri-agonist
Status
Completed
Phase
Phase 1
Enrollment
41
Locations
1
Results
Posted
Publications
0
Study summary
Single ascending dose of HM15211 in healthy obese subjects.
A First-in-human study to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics after single ascending dose of HM15211 in healthy obese subjects.
Interventions
BIOLOGICAL
Long-acting tri-agonist
Timeline
First posted
Dec 15, 2017
Study start
Apr 4, 2018
Primary completion
Sep 14, 2018
Study completion
Sep 14, 2018
Results posted
May 17, 2024
Registry updated
Feb 6, 2025
Outcomes
Number of Participants With Adverse Events
Time frame · 1 month
An adverse event is any undesirable and unintended medical event occurring to a subject in a clinical study, whether or not related to the investigational products
Not reported in the indexed record.
Eligibility
Inclusion Criteria: * Female subjects must be non-pregnant and non-lactating Exclusion Criteria: * Participation in an investigational study within 30 days prior to dosing
Study locations
United States. Showing up to 24 locations stored in the fast local snapshot.
Hanmi Investigative Site
Chula Vista, California, United States
Publications
No PMID-linked publications were present in this registry snapshot.
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Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.