Faecal Microbiota Transplantation for Immune Checkpoint Inhibitor-mediated Diarrhea/Colitis: a Randomised, Double-blind Pilot Efficacy and Safety Study

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to determine the outcome of patients with immune checkpoint inhibitor-mediated diarrhea/colitis (IMC) treated with faecal microbiota transplantation (FMT) in a randomised, placebo-controlled trial. The aim of the present study is to assess the feasibility, pilot efficacy, and safety of FMT for patients with IMC. Participants will be treated two times with capsule FMT or placebo capsules in a 1:1 ratio. The intervention treatment will be an add-on to the patients' standard treatment for IMC. Researchers will compare the FMT-treated group to the placebo-treated group to see if FMT promotes remission of IMC.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age 18 years or above.

• Histologically proven diagnosis of malignant melanoma and/or kidney cancer.

• Treatment with any immune checkpoint inhibitor (Nivolumab, Pembrolizumab, Cemiplimab, Atezolizumab, Durvalumab, Avelumab, Ipilimumab), alone or in combination, within the last 8 weeks.

• Grade 2 or higher CTCAE diarrhea, of which at least 3 stools are Bristol chart score 6-7.

• Negative PCR for enteric pathogens including C. difficile, after the onset of diarrhea.

• Signed written informed consent.

Locations
Other Locations
Denmark
Aarhus University Hospital
RECRUITING
Aarhus N
Contact Information
Primary
Trine L Laursen, BSc
trnlau@rm.dk
+4540408207
Backup
Christian L Hvas, PhD
christian.hvas@auh.rm.dk
+4528351839
Time Frame
Start Date: 2024-01-23
Estimated Completion Date: 2025-03-31
Participants
Target number of participants: 20
Treatments
Experimental: Faecal microbiota transplantation (FMT)
Patients receive two applications of capsule FMT with 3-7 days between applications.
Placebo_comparator: Placebo
Patients receive two applications of placebo capsules with 3-7 days between applications.
Sponsors
Leads: University of Aarhus

This content was sourced from clinicaltrials.gov

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