Current partner codePEPTIDESDE
NCT03374241·Phase 1·INTERVENTIONAL

A First-in-human Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of HM15211(Efocipegtrutide)

Status

Completed

Phase

Phase 1

Enrollment

41

Locations

1

Results

Posted

Publications

0

Study summary

What the protocol is testing.

Single ascending dose of HM15211 in healthy obese subjects.

Full detailed description

A First-in-human study to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics after single ascending dose of HM15211 in healthy obese subjects.

Interventions

Treatment arms and agents.

BIOLOGICAL

HM15211 or Placebo

Long-acting tri-agonist

Timeline

From registration to results.

  1. First posted

    Dec 15, 2017

  2. Study start

    Apr 4, 2018

  3. Primary completion

    Sep 14, 2018

  4. Study completion

    Sep 14, 2018

  5. Results posted

    May 17, 2024

  6. Registry updated

    Feb 6, 2025

Outcomes

What the study measures.

Primary 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

Secondary outcomes

Not reported in the indexed record.

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
65 Years
Sex
ALL
Healthy volunteers
Yes

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

1 registered sites.

United States. Showing up to 24 locations stored in the fast local snapshot.

Hanmi Investigative Site

Chula Vista, California, United States

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Efocipegtrutide.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.