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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

Interventions

DRUG

Biological: GB261

GB261 will be dosed according to the protocol