Fecal Transplant +/- Gut Decontamination in Preventing Acute Graft Versus Host Disease in Patients Given Broad-Spectrum Antibiotics

Withdrawn before enrolling · Phase 2

Conditions studied: Graft-versus-host Disease Prevention

In brief

This phase II trial studies how well a fecal microbiota transplant with or without total gut decontamination works in preventing graft versus host disease in patients exposed to broad-spectrum antibiotics. Fecal microbiota transplantation is the administration by enema of fecal matter (stool) that includes helpful bacteria from a normal, healthy donor. Total gut decontamination uses antibiotics to remove/reduce the amount of bacteria in the digestive system. It is not yet known if a fecal microbiota transplant with or without total gut decontamination works better in preventing graft versus host disease compared to standard immunosuppressive therapies (therapies that lower the normal function of the immune system).

Key facts

Study ID

NCT03862079

Run by

M.D. Anderson Cancer Center

People needed

0

Starts

2020-06-01

Expected to finish

2021-12-31

Last updated by the study team

2020-03-04

Who can join

Age: 16 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients who are day -10 pre- to day +30 post-allogeneic hematopoietic cell transplant (AHCT) from any donor or graft source and for any conditioning regimen
• Patients who have received treatment with meropenem or piperacillin-tazobactam (pip-tazo) intravenously (IV) (of at least 24 hours duration) in past 7 days
• Controlled infection defined as hemodynamically stable and not requiring supplemental oxygen of more than 2 liters via nasal cannula
• Patients who are able to take oral medications in suspension form
• Patients who are able to provide informed consent (IC) and comply with all study visits and procedures

You may not qualify if…

• Patients who are anticipated to require continued broad spectrum antibiotics with meropenem or pip-tazo IV for > 96 hours post-engraftment such as for known, documented infections necessitating prolonged treatment
• Patients with a prior documented infection with mycormycetes
• Patients who are greater than 2 days from time of neutrophil engraftment post AHCT
• Patients with active enteric infections
• Patients with acute GVHD >= grade II
• Patients unwilling or unable to undergo the FMT via retention enema procedure
• Patients who have received treatment with an investigational agent within 2 weeks of enrollment
• Patients unable to tolerate oral decontamination regimen of pip-tazo and nystatin due to prior allergy or intolerance of these medications
• Patients with any medical or psychological condition that, in the opinion of the investigator, might interfere with the subject's participation in the trial, pose any additional risk for the subject, or confound the assessments of the subject

Where it is running

• M D Anderson Cancer Center — Houston, Texas, United States

Full record on ClinicalTrials.gov

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