An Open-label Study of CND261 in Seropositive Rheumatoid Arthritis

NCT07052032 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 47

Last updated 2026-04-16

No results posted yet for this study

Summary

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

Conditions

Interventions

BIOLOGICAL

CND261

CND261 will be dosed according to the assigned cohort

Sponsors & Collaborators

  • Candid Therapeutics

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-06-16
Primary Completion
2027-06-01
Completion
2027-06-01

Countries

  • Georgia
  • Moldova
  • Ukraine

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07052032 on ClinicalTrials.gov