Clinical trial

A Phase 3 Open-Label Clinical Study to Evaluate the Safety and Tolerability of Rebiotix RBX2660 (Microbiota Suspension) in Subjects With Recurrent Clostridium Difficile Infection

Name
2019-01
Description
This is a prospective, multicenter, open-label Phase 3 study of a microbiota suspension of intestinal microbes. Patients who have had at least one recurrence of CDI after a primary episode and have completed at least one round of standard-of-care oral antibiotic therapy or have had at least two episodes of severe CDI resulting in hospitalization may be eligible for the study. Subjects may receive a second RBX2660 enema if they are deemed treatment failures following the initial enema per the protocol-specified treatment failure definition.
Trial arms
Trial start
2019-07-30
Estimated PCD
2023-07-21
Trial end
2023-07-21
Status
Completed
Phase
Early phase I
Treatment
RBX2660
RBX2660 is a microbiota suspension administered as an enema
Arms:
Active
Other names:
Microbiota suspension
Size
817
Primary endpoint
Safety and tolerability of RBX2660 in subjects with recurrent CDI.
Up to 6 months after last study treatment.
Eligibility criteria
Inclusion Criteria: 1. ≥ 18 years old. 2. Medical record documentation of either: a) a current diagnosis or history of recurrent CDI as determined by the treating physician, b) or has had at least two episodes of severe CDI resulting in hospitalization. 3. Is currently taking or was just prescribed antibiotics to control CDI related diarrhea at the time of enrollment. \[Note: Subject's CDI diarrhea must be controlled (\<3 unformed/loose stools/day) while taking antibiotics during screening.\] Exclusion Criteria: 1. Has continued CDI diarrhea despite being on a course of antibiotics prescribed for CDI treatment. 2. Requires systemic antibiotic therapy for a condition other than CDI. 3. Fecal microbiota transplant (FMT) within the past 6 months. 4. FMT with an associated serious adverse event related to the FMT product or procedure. 5. Bezlotoxumab (CDI monoclonal antibodies) if received within the last year. 6. CD4 count \<200/mm\^3 during Screening. 7. An absolute neutrophil count of \<1000 cells/µL during Screening. 8. Pregnant, breastfeeding, or intends to become pregnant during study participation.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE3'], 'designInfo': {'allocation': 'NA', 'interventionModel': 'SINGLE_GROUP', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 817, 'type': 'ACTUAL'}}
Updated at
2024-01-23

1 organization

1 product

3 indications

Organization
Rebiotix
Product
RBX2660
Indication
Infection