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REBYOTA™ Prospective Registry

Completed · NCT05835219

Conditions: Recurrence of Clostridium Difficile Infection

At a glance

Research payments reported, 2025
$234,684
U.S. investigators named
38
Sites paid
37
Planned or actual enrollment
145

About the trial

Sponsor
Ferring Pharmaceuticals
Tested
REBYOTA™ (drug)
Dates
Started 2023-06-19; completion 2025-08-29
Results posted
Not yet

This is a prospective observational cohort study designed to collect data on patients who received REBYOTA™ for the prevention of rCDI in the routine care setting. As all data collected for this study are observational, the decision to prescribe REBYOTA™ is at the treating physician's discretion and independent from the decision to enroll the patient in the study. Data will be collected from patients' medical records after obtaining informed consent. Data about clinical history, CDI events (primary and recurrent: severity, treatment), CDI-related symptoms, treatments, medical procedures, Adverse Events(AEs), and healthcare resource utilization (i.e., hospitalizations and re-admissions) wi…

From ClinicalTrials.gov, last updated 2026-01-28. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Ferring Pharmaceuticals As reported $234,684 in research payments for this study in 2025 (121 payments).

Products named: Rebyota

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.