Fexofenadine in Patients With Active Rheumatoid Arthritis

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18-60
SponsorOctober 6 University

About this trial

Rheumatoid arthritis (RA) is an inflammatory autoimmune polyarthritis affecting ∼1% of the world population, resulting in the loss of joint function and progressive structural damage in affected joints. Fexofenadine has been widely used to treat various allergic diseases, like allergic rhinitis, conjunctivitis and chronic idiopathic urticaria. the molecular mechanisms underlying fexofenadine mediated inhibition of TNF-α signalling

Eligibility criteria

Qualifiers

Moderate to severe RA (disease activity score-28 joints: DAS-28 > 3.2) were recruited.

Age between 18 - 60 years having active disease according to the diagnosis of an experienced rheumatologist, being under treatment with disease-modifying anti-rheumatic drugs (DMARDs), not receiving cytokine inhibitors

Signing informed consent and willingness of the participant to accept randomization to any assigned treatment arm.

Disqualifiers

History of biological DMARDS.

History/presence of acute heart disease, liver and kidney diseases, COPD

Intolerance or allergy to fexofenadine or methotrexate

Alcohol abuse

Trial design

Treatments tested in this trial

  • Fexofenadine
  • Placebo

Treatment groups

80 Participants
are divided into 2 treatment groups

Sponsors and collaborators