PKUCare Luzhong Hospital
Zibo, China
NCT Number: NCT05715333
This study is a single-center, randomized, double-blind, placebo-controlled, dose-increasing phase I clinical study.
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Notify Me18 year–65 year
Male
Interventional
Phase 1
Zibo, China
The purpose of this study is to evaluate the safety, tolerance, pharmacokinetics and immunogenicity of single and multiple subcutaneous administration of CM326 at different doses in healthy male subjects.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
CM326 Injection
Subcutaneous injection
Time frame: Up to week 12
By assessing the number and severity of adverse events during the study.
Keymed Biosciences Co.Ltd
Industry
A Randomized, Double-blind, Placebo-controlled Phase I Clinical Study to Evaluate the Safety, Tolerance, Pharmacokinetics and Immunogenicity of CM326 Injection in Healthy Subjects
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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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