Poop pills for cancer patients? pilot study tests fecal transplants in High-Risk therapies
NCT ID NCT07509450
First seen Jun 27, 2026 · Last updated Jul 09, 2026 · Updated 2 times
Summary
This pilot study is testing whether fecal microbiota transplantation (FMT) — giving processed stool from a healthy donor via enema — is safe and doable in 20 patients with lymphoma or leukemia who are receiving CAR-T therapy or stem cell transplants. The goal is to see if at least half of approached patients join, most stay in the study, and the procedure doesn't cause serious harm. It's an early step to explore if restoring gut bacteria can help these vulnerable patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Fecal microbiota transplant (FMT) enema
- What this could lead to
- If successful, this could show that FMT is a safe way to restore gut health in patients undergoing intensive cancer therapies, potentially reducing complications.
- What could go wrong
- This is a very small pilot study with only 20 participants, so results may not apply broadly. There is a risk of serious side effects like infection or bowel injury from the procedure.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 20 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2026
- Expected to finish
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Jun 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Men and women ≥ 18 years of age 2. Diagnosis of the following: 1. Indolent or aggressive B-cell lymphoma eligible for standard or care CAR-T therapy (Cohort A), or 2. Patients with AML or high risk MDS with indication to undergo reduced-intensity conditioning alloSCT, with an available matched related, unrelated, or haploidentical donor (Cohort B) 3. ECOG 0-1 4. Adequate marrow function defined by: 1. Hemoglobin \>80 g/L without transfusion dependence within the last 7 days 2. Platelet count \>20 x 109/L without transfusion dependence within the last 7 days 3. Neutrophil count \>1.0 x 109/L without growth factor support within the last 7 days 5. Adequate liver function as indicated by aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 x the institutional upper limits of normal (ULNs) value; serum total bilirubin \< 1.5 x ULN (unless documented Gilbert's syndrome) 6. Adequate renal function as defined as creatinine clearance ≥ 30 mL/min directly measured with a 24-hour urine collection or calculated according to the modified formula of Cockcroft-Gault equation or Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) calculation 7. Life expectancy \>6 months 8. Women of childbearing potential (WOCBP) who are sexually active must use highly effective methods of contraception during treatment and up to 6 months after the last dose of protocol therapy. Men who are sexually active must use highly effective methods of contraception during treatment and up to 6 months after the last dose of protocol therapy. Men require an agreement to remain abstinent (ie, refrain from heterosexual intercourse) or use a condom, and an agreement to refrain from donating sperm. Periodic abstinence and withdrawal are not acceptable methods of contraception. Fertility preservation options should be discussed. Examples of highly effective contraceptive methods include an agreement to remain abstinent (ie, refrain from heterosexual intercourse), bilateral tubal ligation, male sterilization, established proper use of hormonal contraceptives that inhibit ovulation, hormone-releasing intrauterine devices, and copper intrauterine devices. 9. Willing and able to participate in all required evaluations and procedures in this study. 10. Ability to understand and the willingness to sign a written informed consent. Exclusion Criteria: 1. For patients undergoing alloSCT (Cohort B): plan to undergo myeloablative conditioning 2. Use of investigational agents within the last 4 weeks before enrollment. 3. Active or uncontrolled infection 4. Autoimmune disorder currently being treated with disease-modifying therapy or with \>10mg/day prednisone 5. Inflammatory bowel disease 6. History of intestinal perforation 7. Gastrointestinal surgical procedure within the past 4 weeks before enrollment 8. Pregnant or breast-feeding patients 9. HIV infection with detectable viral load or CD4 count \<200 10. Serologic status reflecting active hepatitis B or C infection as follows: 1. Presence of hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (HBcAb) with detectable hepatitis B virus (HBV) DNA. (Note, patients with undetectable HBV DNA are permitted to enroll if they are on Hepatitis B suppressive therapy) 2. Patients with presence of hepatitis C virus (HCV) antibody and HCV RNA detectable 11. History of infection or known colonization with antibiotic resistant organism in the last two years before enrollment (including ESBL, MRSA, VISA, VRSA, VRE, CPE) 12. Any serious medical condition or abnormality in clinical laboratory tests that, in the investigator's judgment, precludes the patient's safe participation in the study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University Health Network
RECRUITINGToronto, Ontario, M5G 2M9, Canada
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