Microbiota Restoration Therapy for Recurrent Clostridium Difficile Infection
Status: | Active, not recruiting |
---|---|
Conditions: | Infectious Disease |
Therapuetic Areas: | Immunology / Infectious Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 7/27/2016 |
Start Date: | October 2015 |
End Date: | June 2018 |
An Open-label Efficacy and Safety Assessment of Rebiotix RBX2660 (Microbiota Suspension) for the Treatment of Recurrent Clostridium Difficile Infection
This study will evaluate efficacy and safety information about RBX2660 for the treatment of
recurrent Clostridium difficile infection (CDI). Enrolled subjects will receive one
treatment with RBX2660 (microbiota suspension).
recurrent Clostridium difficile infection (CDI). Enrolled subjects will receive one
treatment with RBX2660 (microbiota suspension).
This is a prospective, multicenter, open-label study assessing the efficacy and safety of
RBX2660 as an adjunct to antibiotics for the treatment of recurrent CDI. The primary
assessments for this study are (i) to assess efficacy as the absence of CDI diarrhea without
the need for retreatment with C. difficile anti-infective therapy or fecal transplant
through 56 days after completion of study treatment with RBX2660 and (ii) safety via
assessment of adverse events. Patients who have had either a) at least two recurrences after
a primary episode (i.e., at least three episodes) and have completed at least two rounds of
standard-of-care oral antibiotics or b) have had at least two episodes of severe CDI
resulting in hospitalization may be eligible to participate in the study. Study visits are
1- and 8-weeks after treatment with additional follow-up assessments at 3,6,12, and 24
months post treatment.
RBX2660 as an adjunct to antibiotics for the treatment of recurrent CDI. The primary
assessments for this study are (i) to assess efficacy as the absence of CDI diarrhea without
the need for retreatment with C. difficile anti-infective therapy or fecal transplant
through 56 days after completion of study treatment with RBX2660 and (ii) safety via
assessment of adverse events. Patients who have had either a) at least two recurrences after
a primary episode (i.e., at least three episodes) and have completed at least two rounds of
standard-of-care oral antibiotics or b) have had at least two episodes of severe CDI
resulting in hospitalization may be eligible to participate in the study. Study visits are
1- and 8-weeks after treatment with additional follow-up assessments at 3,6,12, and 24
months post treatment.
Inclusion Criteria:
- ≥ 18 years old.
- Medical record documentation of recurrent CDI including a positive C. difficile test
within 60 days prior to enrollment and either: a) at least two recurrences after a
primary episode and has completed at least two rounds of standard-of-care oral
antibiotic therapy or b) has had at least two episodes of severe CDI resulting in
hospitalization.
- Documented history that the subject's recurrent CDI is controlled while on
antibiotics even if the subject is not currently on antibiotics.
- A positive stool test for the presence of C. difficile within 60 days prior to
enrollment
Exclusion Criteria:
- A known history of continued CDI diarrhea despite being on a course of antibiotics
prescribed for CDI treatment.
- Requires continuous antibiotic therapy for a condition other than CDI.
- Previous successful (resolution of CDI diarrhea) fecal transplant for recurrent CDI <
6 months prior to study enrollment.
- Previous unsuccessful (recurrent CDI diarrhea was unresolved) fecal transplant.
- Previous treatment with RBX2660.
- Diagnosis of inflammatory bowel disease (IBD), e.g., ulcerative colitis, Crohn's
disease, or microscopic colitis.
- Diagnosis of irritable bowel syndrome (IBS) as determined by Rome III criteria.
- History of chronic diarrhea.
- History of celiac disease.
- Disease symptoms caused by a confirmed intestinal pathogen other than C. difficile.
- Colostomy.
- Planned surgery requiring perioperative antibiotics within 3 months of study
enrollment.
- Life expectancy of < 12 months.
- Compromised immune system
We found this trial at
29
sites
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials