BENITIONSClinical Trial Intelligence

Effects of Administration of SCFA in Rheumatoid Arthritis Inadequate Responders

Не применимо Завершено NCT05718583

ЗаболеваниеRheumatoid Arthritis
ФазаНе применимо
СпонсорNYU Langone Health
СтатусЗавершено
Участники20 участн.
ВмешательствоButyrate
Дата начала1.02.2023
Дата завершения20.02.2025
Публикация результатов2.06.2026

Кратко

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.

Change From Baseline in Microbiome Alpha Diversity

Baseline, Month 1 Post-Treatment Initiation · index

RA Patients Who Are Inadequate Responders to Current RA Treatment0.19 index

Открыть в BENITIONS Открыть на ClinicalTrials.gov

Другие исследования по этому заболеванию

Все исследования

Страница обобщает открытые данные ClinicalTrials.gov. Это не медицинская и не инвестиционная рекомендация. Обратитесь к врачу.