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Study identifier: NCT07669571 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Not Yet Recruiting

A Phase I Study of NS-079 in Healthy Participants

Condition: Healthy Adult Participants  ·  Sponsor: NeuShen Therapeutics

PhasePhase 1
Planned participants78
Who can joinAll sexes, 18 Years to 55 Years
Healthy volunteersYes

About this study

The goal of this clinical trial is evaluate the safety, pharmacokinetics, and pharmacodynamics of NS-079 with its main metabolite (NS-079-M1) in healthy participants. The main questions it aims to answer are: * Is NS-079 safe and tolerable in heathy participants under tested dosing regimen? * What is the pharmacokinectic profile of NS-079 in healthy participants under tested dosing regimen and the effect of paroxetine? Researchers will compare NS-079 to a placebo to see the safety and tolerability when use NS-079.

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

Talk to the study team

Jin Lili, MS  ·  +86 13918207440  ·  lili.jin@neushen.com

Always discuss trial participation with your own doctor first.

Locations (1)

CMAX Clinical Research Pty LtdAdelaide, South Australia, Australia

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