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Study identifier: NCT07729839 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Safety, Tolerability, and Pharmacokinetic Evaluation of ADB116 for Injection

Condition: Healthy Adult Participants  ·  Sponsor: Jiangsu Aidea Pharmaceutical Group Co., Ltd.

PhasePhase 1
Planned participants26
Who can joinAll sexes, 18 Years to 45 Years
Healthy volunteersYes

About this study

A Phase I Study of ADB116 for Injection in Healthy Chinese Adults. This study aims as follows: Primary Objective: • To evaluate the safety and tolerability of a single intravenous bolus dose of ADB116 for injection in healthy Chinese adults. Secondary Objective: • To evaluate the pharmacokinetic (PK) profile of a single intravenous bolus dose of ADB116 for injection.

This description comes directly from the study's public registry record.

Talk to the study team

Xinmin Yun, Ph.D  ·  +86 0514-87752666  ·  yunxm@aidea.com.cn

Bing Yang, M.Sc  ·  +86 025-83193180  ·  yangbing@aidea.com.cn

Always discuss trial participation with your own doctor first.

Locations (1)

NanFang Hospital of Southern Medical UniversityGuangzhou, Guangdong, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07729839