Actively Recruiting

Age: 18Years +
All Genders
NCT05936970

Prospective, Multi-Center, Observational, Whole Blood Specimen Collection Study in Participants with Rheumatoid Arthritis with Inadequate Response or Intolerance to a DMARD Starting a New BDMARD or TsDMARD Treatment +/- CsDMARD

Led by Aqtual, Inc. · Updated on 2024-11-29

1410

Participants Needed

1

Research Sites

126 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The primary goal of this study is to assess a cfDNA-based blood test using genetic, transcriptomic and/or epigenetic information to help doctors predict the best treatment options for rheumatoid arthritis (RA) patients with inadequate response or intolerance to previous therapies.

CONDITIONS

Official Title

Prospective, Multi-Center, Observational, Whole Blood Specimen Collection Study in Participants with Rheumatoid Arthritis with Inadequate Response or Intolerance to a DMARD Starting a New BDMARD or TsDMARD Treatment +/- CsDMARD

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ability to understand and provide written informed consent.
  • Male or female 18 years of age or older at enrollment.
  • Diagnosis of Rheumatoid Arthritis at the time of enrollment.
  • Prior treatment with at least 1 csDMARD, bDMARD, or tsDMARD.
  • Planning to start a new bDMARD (+/- csDMARD) or tsDMARD (+/- csDMARD) within 1 month after enrollment.
  • Moderate to high Clinical Disease Activity Index (CDAI) greater than 10 with at least 4 tender joints and 4 swollen joints at screening.
Not Eligible

You will not qualify if you...

  • Unsuitable for participation in the opinion of the principal investigator.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Arthritis and Osteoporosis Consultants of the Carolinas

Charlotte, North Carolina, United States, 28207

Actively Recruiting

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Research Team

A

Aqtual Study Support

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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