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Active Not RecruitingNCT07052032

An Open-label Study of CND261 in Seropositive Rheumatoid Arthritis

A Phase 1b, Open-Label, Multicenter Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, Immunogenicity, and Preliminary Clinical Activity of CND261 in Patients With Seropositive Rheumatoid Arthritis

Status
Active Not Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
47 (estimated)
Sponsor
Candid Therapeutics · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to evaluate the safety and efficacy of CND261 in patients with seropositive rheumatoid arthritis.

Detailed description

This is a Phase 1b, open-label, multicenter study evaluating the safety, tolerability, pharmacokinetics, pharmacodynamics, immunogenicity, and preliminary clinical activity of CND261 in patients with seropositive rheumatoid arthritis. The study consists of 2 parts: a dose-escalation part and an open-label expansion. Patients will be followed until Week 52.

Conditions

Interventions

TypeNameDescription
BIOLOGICALCND261CND261 will be dosed according to the assigned cohort

Timeline

Start date
2025-06-16
Primary completion
2027-06-01
Completion
2027-06-01
First posted
2025-07-04
Last updated
2026-04-16

Locations

3 sites across 3 countries: Georgia, Moldova, Ukraine

Source: ClinicalTrials.gov record NCT07052032. Inclusion in this directory is not an endorsement.

An Open-label Study of CND261 in Seropositive Rheumatoid Arthritis (NCT07052032) · Clinical Trials Directory