The First Affiliated Hospital of Yunnan University of Chinese Medicine (Yunnan Provincial Hospital of Traditional Chinese Medicine)
Kunming, Yunnan, China
NCT Number: NCT07787624
This is a randomized, double-blind, placebo-controlled, single- and multiple- dose-escalating Phase 1a study. The objective is to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and immunogenicity of MWN109 Injection in healthy Chinese volunteers and to provide data for subsequent clinical trials.
The study includes a single ascending dose (SAD) part with 4 dose cohorts and a multiple ascending dose (MAD) part with 3 dose cohorts, using a 3-week dose titration regimen.
Approximately 58 volunteers will be enrolled. The primary endpoint is safety, assessed by adverse events, serious adverse events, vital signs, physical examinations, laboratory tests, and 12-lead electrocardiograms. The secondary endpoint is the pharmacokinetic characteristics.
Looking for future studies?
Notify Me18 year–45 year
All sexes
Interventional
Phase 1
Kunming, Yunnan, China
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
S1, S2 S3, S4; administered subcutaneously (SC)
administered SC
Time frame: From Day 1 to Day 43
The incidence of adverse events (AEs) and serious adverse events (SAEs).
Time frame: From Day 1 to Day 29
Cmax of MWN109.
Time frame: From Day 1 to Day 29
Tmax of MWN109.
Time frame: From Day 1 to Day 29
AUC0-t of MWN109.
Time frame: From Day 1 to Day 29
AUC0-inf of MWN109.
Time frame: From Day 1 to Day 29
t1/2 of MWN109.
Time frame: From Day 1 to Day 43
Cmax,ss of MWN109.
Time frame: From Day 1 to Day 43
Cmin,ss of MWN109.
Time frame: From Day 1 to Day 43
Cav,ss of MWN109.
Time frame: From Day 1 to Day 43
Tmax,ss of MWN109.
Time frame: From Day 1 to Day 43
t1/2,ss of MWN109.
Time frame: From Day 1 to Day 43
AUC0-τ,ss of MWN109.
Time frame: From Day 1 to Day 43
AUC0-t,ss of MWN109.
Shanghai Minwei Biotechnology Co., Ltd
Industry
A Randomized, Double-Blind, Placebo-Controlled Phase 1a Clinical Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Single and Multiple Subcutaneous Dose Escalation of MWN109 Injection in Healthy Chinese Volunteers
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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