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Not Yet RecruitingNCT07476586

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics of GenSci161 in Healthy Adult Participants

A Single-center, Randomized, Double-blind, Placebo-controlled, Dose-escalation Phase 1 Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, and Biomarker Characteristics of a Single Subcutaneous Injection of GenSci161 Injection in Healthy Adult Participants

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
44 (estimated)
Sponsor
Changchun GeneScience Pharmaceutical Co., Ltd. · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

To Evaluate the Safety and Tolerability, Pharmacokinetics and Biomarker of GenSci161 in a Randomized, Double-blind, Placebo-controlled Study in Healthy Adult Participants.

Conditions

Interventions

TypeNameDescription
DRUGGenSci161Administered subcutaneous injection
DRUGPlaceboAdministered subcutaneous injection

Timeline

Start date
2026-04-23
Primary completion
2027-05-06
Completion
2027-08-10
First posted
2026-03-17
Last updated
2026-03-17

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07476586. Inclusion in this directory is not an endorsement.