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

Sponsor
Sadat City University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04757571
Collaborator
(none)
120
1
2
22.9
5.2

Study Details

Study Description

Brief Summary

Among three MAPK families, paroxetine was found to be able to decrease the phosphorylation of ERK. It was reported that paroxetine attenuates the symptoms of collage induced arthritis rats due to its inhibitory effect on T cell activation and infiltration to synovial tissue via suppression of ERK pathway. This study aimed to evaluate the therapeutic efficacy of paroxetine in rheumatoid arthritis. Paroxetine prevents the joint inflammation which is at the very early stage. paroxetine could inhibit GRK2 with selectivity over other GRKs. Medications developed for maintaining the immunologic equilibrium. such as GRK2 inhibitors, will be the novel trends in RA treatment that could avoid the adverse side effects that are common with current treatment options.

Condition or Disease Intervention/Treatment Phase
Phase 1/Phase 2

Study Design

Study Type:
Interventional
Anticipated Enrollment :
120 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
The GRK2 Inhibitor Paroxetine as a Novel Adjunct to Conventional Therapy in Rheumatoid Arthritis Patients. A Proof-of-Concept, Randomized, Double-Blind, Placebo-Controlled Trial.
Actual Study Start Date :
Feb 1, 2021
Anticipated Primary Completion Date :
Oct 31, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Paroxetine

Paroxetine 20 mg daily plus standard therapy

Drug: Paroxetine
Paroxetine 20 mg tablet plus standard therapy

Placebo Comparator: Placebo

Placebo tablet daily plus standard therapy

Drug: Placebo
Placebo tablet plus standard therapy

Outcome Measures

Primary Outcome Measures

  1. ACR 20% improvement criteria (ACR20) response rate [week 12]

    based on tender and swollen joint counts, patient's assessment of pain, patient and physician global assessment of arthritis, Health Assessment Questionnaire Disability Index (HAQ DI), and CRP level

  2. ACR50 & ACR70 response rate [week 12]

    based on tender and swollen joint counts, patient's assessment of pain, patient and physician global assessment of arthritis, Health Assessment Questionnaire Disability Index (HAQ DI), and CRP level

  3. Disease activity scale in 28 joints (DAS-28) [week 12]

    Scale assessing severity of rheumatoid arthritis based on number of tender, swollen joints, erythrocyte sedimentation rate (ESR) levels, and patient self-assessment of his condition (global health assessment). Whereas "28" describes the number of different joints including in the measurement: proximal interphalangeal joints (10 joints), metacarpophalangeal joints (10), wrists (2), elbows (2), shoulders (2), knees (2).

Secondary Outcome Measures

  1. GRK2 expression [week 12]

    GRK2 expression in serum

  2. TNF-α [week 12]

    Serum level Tumor necrosis factor- alpha (TNF-α)

  3. Inteleukins [12 weeks]

    Serum levels of Interleukins (IL) IL-17, IL-1β , IL-6 & IL-10

  4. CRP [12 weeks]

    Serum level of C-reactive protein (CRP)

  5. Drug Adverse effects [12 weeks]

    Adverse effect incidence: adverse effect will be reported by patients or their caregivers and recorded by investigator.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

• Patients with active rheumatoid arthritis based on DAS28 score. Patients received the standard therapy (i.e. one or more conventional DMARDs) for at least three months.

Exclusion Criteria:
  • Known hypersensitivity to metformin.

  • Patients who have a prior diagnosis with diabetes mellitus.

  • Patients receive metformin for any other indications.

  • Patients with congestive heart failure.

  • Patients with a history of myocardial infarction.

  • Patients with severe anemia.

  • Patients with active infections or other inflammatory diseases.

  • Patients receiving biological therapy.

  • Pregnancy or lactation.

  • Patients with impaired liver functions.

  • Patients with impaired kidney functions (serum creatinine concentrations ≥1.5 and ≥1.4 mg/dL in males and females respectively).

  • Patients with malignancies.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Faculty of Pharmacy Shibīn Al Kawm Menoufia Egypt 13829

Sponsors and Collaborators

  • Sadat City University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Mahmoud Samy Abdallah, Lecturer of Clinical Pharmacy, Sadat City University
ClinicalTrials.gov Identifier:
NCT04757571
Other Study ID Numbers:
  • RS10/2021
First Posted:
Feb 17, 2021
Last Update Posted:
Feb 22, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 22, 2022