LivingGLP1
Study S003251

A Single Center, Randomized, Double Blind, Placebo Controlled, Multiple Dose Escalating Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of PB-718 Injection in Chinese Obese Subjects.

Registration

Registration
NCT06147544
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1; PHASE2
Masking
DOUBLE
Status
COMPLETED
Enrollment
36
Start
2023-07-06
Primary completion
2024-04-16
Lead sponsor
PegBio Co., Ltd.
Conditions
Obesity
Interventions
DRUG:PB-718; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Incidence of Treatment-Emergent Adverse Events [From the first dosing (Day 1 ) of study drug until completion of the post treatment follow-up visit (20 weeks for cohort 1 and cohort 2 or 26 weeks for cohort 3)]

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
R0032846768-P: A Phase 1b/2a Trial to Assess the Safety, Tolerability, Pharmacokinetics, and Efficacy of PB-718, a GLP-1R/GCGR Dual Agonist in Subjects with Obesity
STUDY GROUP PB-718, Diabetes
2024Randomized trialDOIcites ClinicalTrials.gov:NCT06147544