A Pilot Proof of Concept Study of the Effects of Administration of a Short Chain Fatty Acid (SCFA) Supplement in Rheumatoid Arthritis Inadequate Responders (EASi-RAIR)

Status: Recruiting
Location: See location...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study is a pilot, proof of concept study to determine the effects of administering an oral short-chain fatty acid (SCFA) supplement to Rheumatoid Arthritis (RA) patients with inadequate response to methotrexate (MTX). The study will include up to 35 participants to obtain a sample size of at least 25 participants taking the oral supplement. The researchers hypothesize that oral SCFA will change the participants' gut microbiome and regulatory immune responses. Clinical data to assess for adverse events, stool, urine samples and peripheral blood will be collected at baseline, 1 month, and with an optional 2 month time-point. Fecal microbiome will be analyzed. Adaptive immune responses will be analyzed from participant blood samples.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Diagnosis of RA meeting 2010 ACR/EULAR for RA and/or treating MD diagnosis

• Inadequate response to MTX per treating MD at maximum tolerated dose.

• Able and willing to provide written informed consent prior to any study specific procedures

• Age 18 years and above at time of enrollment

• Subjects not excluded based on race or ethnicity

Locations
United States
New York
NYU Langone Health Orthopedic Center
RECRUITING
New York
Contact Information
Primary
Rebecca B. Blank, MD, PhD
Rebecca.blank@nyulangone.org
212-598-6149
Time Frame
Start Date: 2023-02-01
Estimated Completion Date: 2025-08-01
Participants
Target number of participants: 35
Treatments
Experimental: RA Patients who are Inadequate Responders to Current RA Treatment
Oral butyrate will be taken at 1000 mg three times daily with meals by RA patients who have active disease and are currently taking methotrexate (MTX) at prescriber's recommended dose. There will be no dose escalation of the study supplement. Clinical data to assess for adverse events, stool, urine samples and peripheral blood will be collected at baseline, 1 month, and with an optional 2-month time-point.
Related Therapeutic Areas
Sponsors
Leads: NYU Langone Health
Collaborators: Arthritis Foundation

This content was sourced from clinicaltrials.gov