Aarhus University Hospital
Aarhus N, 8200, Denmark
Location status: Recruiting
Location contact
Christian L Hvas, PhD
CONTACT
Christian L Hvas, PhD
PRINCIPAL_INVESTIGATOR
Trine L Laursen, BSc
CONTACT
Trine L Laursen, BSc
SUB_INVESTIGATOR
NCT Number: NCT06206707
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Aarhus N, 8200, Denmark
Location status: Recruiting
Christian L Hvas, PhD
CONTACT
Christian L Hvas, PhD
PRINCIPAL_INVESTIGATOR
Trine L Laursen, BSc
CONTACT
Trine L Laursen, BSc
SUB_INVESTIGATOR
As above
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Capsule FMT
Other names: Fecal Microbiota Transplantation, FMT
Placebo capsules
Time frame: At 42 days after intervention treatment
Number of patients with steroid-free resolution of diarrhea, defined as < 3 liquid stools (Bristol <6) per 24 hours during day 40 and 41 after the last intervention treatment.
Time frame: At 42 days after intervention treatment
Number of patients in steroid-free clinical remission of diarrhea 6 weeks (42 days) after the last intervention treatment. Clinical remission is defined as < 4 stools over baseline per day (CTCAE diarrhea grade 1 or less), at day 40 and 41.
Time frame: At 42 days after intervention treatment
Number of patients in steroid-free clinical remission of colitis 6 weeks (42 days) after the last intervention treatment. Clinical remission is defined as asymptomatic in regards to colitis (CTCAE colitis grade 1 or less), at day 40 and 41.
Time frame: Up to 12 weeks after intervention treatment
Therapy response defined as a decrease of at least 3 points in Simple Clinical Colitis Activity Index (SCCAI) score, at weeks 1, 6 and 12 after the last intervention treatment.
Time frame: Up to 12 weeks after intervention treatment
Number of days until less than 4 stools over baseline per day (CTCAE diarrhea grade 1 or less), lasting a minimum of 48 consecutive hours with no increase in steroid dose in the 12 weeks of follow-up.
Time frame: Up to 12 weeks after intervention treatment
Number of days until resolution of diarrhea, defined as 3 or fewer Bristol type 6-7 stools per day, lasting a minimum of 48 consecutive hours.
Time frame: At 42 days after intervention treatment
Number of adverse events (AE) during first 6 weeks after intervention treatment. AE's will be graded by CTCAE.
Time frame: At 12 weeks after intervention treatment
Number of serious adverse events (SAE) during 12 weeks follow-up after the final intervention treatment. SAE's will be graded by CTCAE.
Time frame: Up to 6 weeks after intervention treatment
Changes in faecal microbiome composition from baseline to week 6 after the last intervention.
Time frame: Up to 6 weeks after intervention treatment
Changes in mucosa-associated microbiome from baseline to week 6 after the last intervention.
Time frame: Up to 6 weeks after intervention treatment
Percentual change in faecal-calprotectin from prior to intervention to week 6 after the last intervention.
Time frame: Up to 6 weeks after intervention treatment
Changes in blood immunological parameters (including circulating cytokines) from baseline and at week 6 after the last intervention.
Time frame: Up to 12 weeks after intervention treatment
Hospitalisation defined as the total number of days hospitalised, during 12 weeks of follow-up.
Time frame: Up to 12 weeks after intervention treatment
Colectomy during 12 weeks of follow-up.
Time frame: Up to 12 weeks after intervention treatment
Mortality during the 12 weeks of follow-up.
Time frame: Up to 12 weeks after intervention treatment
Accumulated steroid dose (total dose in mg) during 12 weeks following experimental treatment.
Time frame: Up to 12 weeks after intervention treatment
Number of patients resuming immune checkpoint inhibitor therapy during the 12 weeks of follow-up.
Time frame: Up to 12 weeks after intervention treatment
Response to immune checkpoint inhibitor therapy defined by Response Evaluation Criteria in Solid Tumours (RECIST 1.1 and iRECIST).
Time frame: At 42 days after intervention treatment
Patient and physician perceptions of FMT treatment and the usage for IMC assessed by a patient questionnaire at week 6 and a physician questionnaire.
Time frame: At 42 days after intervention treatment
Changes in health-related quality of life assessed by EQ-5D-5L at baseline and week 6.
Time frame: Up to 6 weeks after intervention treatment
Endoscopic response, defined as decrease in Mayo endoscopic score ≥1 grade, at week 6 after the last intervention treatment.
Time frame: Up to 6 weeks after intervention treatment
Endoscopic remission, defined as Mayo endoscopic score 0, at week 6 after the last intervention treatment.
Contact information is provided by the study sponsor or research team.
Christian L Hvas, PhD
CONTACT
Trine L Laursen, BSc
CONTACT
University of Aarhus
Other
Faecal Microbiota Transplantation for Immune Checkpoint Inhibitor-mediated Diarrhea/Colitis: a Randomised, Double-blind Pilot Efficacy and Safety Study
Acronym: Immunobiome
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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