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Search / Trial NCT06972446

A Study to Evaluate Different Targeted Therapies for Patients With Rheumatoid Arthritis

Launched by ABBVIE · May 7, 2025

Trial Information

Current as of July 25, 2025

Recruiting

Keywords

Rheumatoid Arthritis

ClinConnect Summary

This clinical trial is studying new treatments for people with moderately to severely active rheumatoid arthritis (RA), a condition that causes joint pain, stiffness, and swelling. The trial will test three different therapies: one is lutikizumab, another is ravagalimab, and the last one combines both of these treatments. Some participants will receive a placebo, which looks like the medication but doesn't contain any active ingredients. The goal is to see how well these treatments work and if they are safe for people who have already tried and not responded well to other RA medications.

To be eligible for this trial, participants must have been treated with certain RA medications for at least three months but still have active symptoms. They also need to be on a stable dose of methotrexate, which is a common RA medication. Participants will need to attend regular visits at a hospital or clinic for assessments, blood tests, and to monitor any side effects. It’s important to know that participating in this trial may involve more visits and treatments compared to standard care. The study is not yet recruiting, but it aims to include about 180 participants from around the world.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • At any time prior to the Screening Visit, participant must have been treated for \> or = 3 months with at least 1 b/tsDMARD therapy but continued to exhibit active RA, or had to discontinue due to intolerability or toxicity, irrespective of treatment duration. The maximum cap for prior use of b/tsDMARD is 2.
  • Participant must be on a stable dose of methotrexate (MTX)
  • Exclusion Criteria:
  • Participant is taking nonsteroidal anti-inflammatory drugs (NSAIDs), acetaminophen/paracetamol, low-potency opioids (tramadol, codeine, hydrocodone, alone or in combination with acetaminophen), oral corticosteroids (equivalent to ≤ 10 mg/day of prednisone), or inhaled corticosteroids for stable medical conditions unless they have been on stable doses for ≥ 1 week prior to Baseline Visit.
  • History of any arthritis with onset prior to age 17 years or current diagnosis of inflammatory joint disease other than rheumatoid arthritis.

About Abbvie

AbbVie is a global biopharmaceutical company dedicated to developing innovative therapies that address complex health challenges. Founded in 2013 as a spin-off from Abbott Laboratories, AbbVie focuses on key therapeutic areas, including immunology, oncology, neuroscience, and virology. The company is committed to advancing scientific research and delivering groundbreaking treatments that enhance patient outcomes and quality of life. With a robust pipeline and a strong emphasis on collaboration, AbbVie strives to transform the future of medicine through its commitment to clinical excellence and patient-centered approaches.

Locations

Clearwater, Florida, United States

Fort Collins, Colorado, United States

Tampa, Florida, United States

Grand Blanc, Michigan, United States

Albuquerque, New Mexico, United States

Middleburg Heights, Ohio, United States

Austin, Texas, United States

Houston, Texas, United States

Tomball, Texas, United States

Margate, Florida, United States

Hialeah, Florida, United States

Patients applied

0 patients applied

Trial Officials

ABBVIE INC.

Study Director

AbbVie

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported