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NOT YET RECRUITING
NCT07159009
EARLY_PHASE1
A Study of GB261 in Systemic Sclerosis
Sponsor: Ruijin Hospital
View on ClinicalTrials.gov
Summary
The purpose of this study is to assess the safety, tolerability, PK, PD, immunogenicity, and preliminary clinical activity of GB261 in patients with SSc.
Official title: An Open-Label Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, Immunogenicity, and Preliminary Clinical Activity of GB261 in Systemic Sclerosis
Key Details
Gender
All
Age Range
18 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
10
Start Date
2025-09-04
Completion Date
2027-07-31
Last Updated
2025-09-08
Healthy Volunteers
No
Conditions
Interventions
DRUG
Biological: GB261
GB261 will be dosed according to the protocol