Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06231745

Paroxetine Safety and Efficacy in Rheumatoid Arthritis

The GRK2 Inhibitor Paroxetine as a Novel Adjunct to Conventional Therapy in Rheumatoid Arthritis Patients.

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Mostafa Bahaa · Academic / Other
Sex
All
Age
23 Years – 57 Years
Healthy volunteers
Not accepted

Summary

Rheumatoid arthritis (RA) is a systemic chronic auto-inflammatory disorder which imposes a remarkable burden of morbidity and mortality on global health. The complex interaction between genetics, environment, and immunological response contribute to RA pathogenesis. Current treatment comprises conventional disease-modifying anti-rheumatic drugs (DMARDs) followed by biological DMARDs, if necessary, to achieve low disease activity or remission. Therapeutics used in RA had limitations in tolerability, access, and response duration and magnitude. Consequently, implementation of safe adjunctive treatment for RA is urgently needed to boost the therapeutic response.

Conditions

Interventions

TypeNameDescription
DRUGMethotrexateMethotrexate (MTX) is an anti-metabolite most commonly used in chemotherapy and immunosuppressant in auto-immune diseases. This activity describes the indications, action, and contraindications for Methotrexate as a valuable agent in treating a wide variety of diseases.
DRUGParoxetineParoxetine is a type of antidepressant known as a selective serotonin reuptake inhibitor (SSRI). It's often used to treat depression, and sometimes obsessive compulsive disorder (OCD), panic attacks, anxiety or post-traumatic stress disorder (PTSD).

Timeline

Start date
2024-01-31
Primary completion
2026-02-20
Completion
2026-02-20
First posted
2024-01-30
Last updated
2025-04-08

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06231745. Inclusion in this directory is not an endorsement.