LivingGLP1
Study S003314

A Randomized, Double-Blind, Dose-Escalation, Placebo-Controlled Phase Ia Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of HDM1005 After a Single Subcutaneous Dose in Healthy Subjects

Registration

Registration
NCT06640647
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
65
Start
2024-03-19
Primary completion
2024-08-06
Lead sponsor
Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd.
Conditions
Obesity and Overweight
Interventions
DRUG:HDM1005 injection or placebo
Results posted
FALSE

Registered primary outcomes

  • Safety Outcomes [Signing informed until day 29]

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
R0050051142-OR: Safety, Tolerability, Pharmacokinetics (PK), and Pharmacodynamics (PD) of a Dual GLP-1/GIP Receptor Agonist (HDM1005)—A Phase I, Randomized, Double-Blind, Placebo-Controlled, Single and Multiple Dose-Escalation Study
YIJUN DU, Diabetes
2025Randomized trialDOIcites ClinicalTrials.gov:NCT06640647