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Not Yet RecruitingNCT06297213

R-2487 in Patients With Sjogren's Syndrome (SS)

A Single and Repeat Dosing Study of the Safety, Drug Exposure and Clinical Activity of R-2487 in Patients With Sjogren's Syndrome (SS)

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
36 (estimated)
Sponsor
Rise Therapeutics LLC · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The goal of this study is to determine the safety and tolerability of orally taken probiotic (R-2487) in patients with Sjogren's Syndrome. Patients will take an oral dosage of probiotic (R-2487) and physicians will assess and measure their Sjogren's Syndrome. Blood and fecal evaluations of inflammation and assessment of probiotic (R-2487) on fecal level will also be measured.

Conditions

Interventions

TypeNameDescription
DRUGR-2487R-2487 DP

Timeline

Start date
2026-06-01
Primary completion
2028-08-30
Completion
2028-08-30
First posted
2024-03-07
Last updated
2025-09-04

Regulatory

Source: ClinicalTrials.gov record NCT06297213. Inclusion in this directory is not an endorsement.

R-2487 in Patients With Sjogren's Syndrome (SS) (NCT06297213) · Clinical Trials Directory