Fecal Microbiota Transplantation for Primary Sclerosing Cholangitis - Randomized Study Versus Sham Transplantation
Phase 2 · Testing Fecal microbiota transplantation (FMT) · 1 site · Assistance Publique - Hôpitaux de Paris
Official record & contacts on ClinicalTrials.gov ↗
In plain English
What this trial is testing
This study is testing Fecal microbiota transplantation (FMT) (a drug) as a possible treatment. Condition(s) listed: Primary Sclerosing Cholangitis (PSC) and Inflammatory Bowel Disease (IBD).
Participants are assigned to groups by chance (randomized).
Some participants receive a placebo or sham for comparison.
It is blinded: participants and the study team do not know who receives what.
Phase 2 studies test whether a treatment shows signs of working, and keep checking safety, in a larger group of people with the condition.
Who can join
- Ages 18 to 75
- Any sex
Some of the main requirements, copied from the record:
- Males or females
- Age ≥18 and ≤75 years
- Large duct PSC verified by retrograde, operative, percutaneous or magnetic resonance cholangiography (MRC) demonstrating intrahepatic and /or extrahepatic biliary duct changes consistent with PSC
- IBD diagnosed according to international guidelines (presence of endoscopic and histologic signs)
- IBD inactive for at least 6 months (defined by no evidence of flare and no change in treatment)
- ALP ≥ 1.3 ULN (at least 2 times within a 3 months pre-inclusion period) or elevated total bilirubin ≤50 umol/l (with concomitant elevated direct bilirubin).
Plus 5 more requirement(s). There are also 34 reasons someone might not be able to join (exclusion criteria). Only the trial team can confirm whether you qualify.
What's involved
- About 72 participants are expected to take part.
- The study has 2 groups.
- Start date: 2026-05 (planned).
- Main results expected around 2029-04 (estimate from the record).
- 1 study site listed in France.
Groups in this study
- Fecal microbiota (listed as: experimental group)
- Sham transplantation (listed as: sham comparator group)
Main thing being measured
- To assess in patients with PSC the efficacy of FMT versus sham transplantation on ALP and bilirubin at week 48 addition to standard UDCA therapy. (at week 48)
In the researchers’ words
Primary Sclerosing Cholangitis (PSC) is a rare cholestatic liver disease, commonly associated with inflammatory bowel disease (IBD) The aim of the present trial is to assess the efficacy of fecal microbiota transplantation (FMT) on ALP and bilirubin compared to sham transplantation in addition to ursodeoxycholic acid (UDCA) treatment in PSC patients.
Words you might see
- ALP (alkaline phosphatase): a liver blood test that is often high in PSC.
- ULN: upper limit of normal: the top of the usual range for a lab test.
- UDCA (ursodiol): a bile acid medicine that some people with PSC take.
- Bilirubin: a yellow substance measured in blood; high levels can be a sign of liver or bile-duct problems.
- Cirrhosis: advanced scarring of the liver.
- Decompensated liver disease: advanced liver disease with complications such as fluid build-up or bleeding.
- Cholestasis: reduced or blocked flow of bile.
- Placebo: a look-alike pill or injection with no active drug, used for comparison.
General definitions, not specific to this trial.
This summary was written automatically from the official record using fixed templates (no AI), so it only says what the record says, and may leave things out.
Questions to ask your doctor and the trial team
- Am I likely to qualify, given my health history?
- What would I have to do, and how often would I need to visit?
- Could I get a placebo? What happens to my current treatment?
- What are the possible risks and benefits?
- Are travel or other costs covered?
- What happens after the trial ends?
Official details
| Status | Not yet recruiting |
|---|---|
| Phase | Phase 2 |
| Study type | Interventional |
| Conditions | Primary Sclerosing Cholangitis (PSC); Inflammatory Bowel Disease (IBD) |
| Lead sponsor | Assistance Publique - Hôpitaux de Paris |
| Enrollment | 72 (estimated) |
| Start date | 2026-05 |
| Primary completion (est.) | 2029-04 |
| First posted | 2026-03-17 |
| Last updated | 2026-03-17 |
| Official title | Fecal Microbiota Transplantation for Primary Sclerosing Cholangitis - Randomized Study Versus Sham Transplantation |
| ClinicalTrials.gov ID | NCT07477782 |
Interventions
- Fecal microbiota transplantation (FMT) (Drug)
One to 4 weeks after randomization, the patient will be hospitalized in one of the hepato-gastroenterology department involved in the study for the colonoscopy. The patient will then receive either FMT (suspension of 50g of stools in 300ml of cryopreservative solution) in the terminal ileum or the caecum. At W12 and W24 after first colonoscopy , the patient will receive orally 20 FMT (capsules s… - Sham-transplantation (placebo) (Drug)
One to 4 weeks after randomization, the patient will be hospitalized in one of the hepato-gastroenterology department involved in the study for the colonoscopy. The patient will then receive sham transplantation (FMT vehicle, i.e. 300ml of cryopreservative solution) in the terminal ileum or the caecum. At W12 and W24 after first colonoscopy , the patient will receive orally 20 sham capsules (cap…
Full eligibility criteria (from the record)
Inclusion Criteria: * Males or females * Age ≥18 and ≤75 years * Large duct PSC verified by retrograde, operative, percutaneous or magnetic resonance cholangiography (MRC) demonstrating intrahepatic and /or extrahepatic biliary duct changes consistent with PSC * IBD diagnosed according to international guidelines (presence of endoscopic and histologic signs) * IBD inactive for at least 6 months (defined by no evidence of flare and no change in treatment) * ALP ≥ 1.3 ULN (at least 2 times within a 3 months pre-inclusion period) or elevated total bilirubin ≤50 umol/l (with concomitant elevated direct bilirubin). * Treatment with UDCA (13-23 mg/kg/d) for at least 6 months and at the same dosage for at least 3 months * Using contraceptive in women of childbearing potential and agrees to pursue it from inclusion until week 48. Women of childbearing potential, i.e. fertile, following menarche and until becoming post-menopaused unless permanently sterile, who are sexually active have to apply a highly effective method of birth control with a low failure rate (i.e. less than 1% per year) when used constantly and correctly. * Written informed consent signed * Subject affiliated to the French * Social Security System Exclusion Criteria: * Small duct PSC * Autoimmune hepatitis defined by the presence of moderate to severe interface hepatitis documented on liver biopsy and at least 1 of the 2 following criteria: AST or ALT > 5 ULN, Positive anti smooth muscle auto antibodies or serum IgG > 1.5 ULN * Secondary sclerosing cholangitis (notably IgG4-associated cholangitis) * Cirrhosis defined by Liver elastometry >14.4 kPa or by current or past decompensation of cirrhosis * AST or ALT > 7 ULN in the last 3 months * Platelets count in the last 3 months < 100 000/mm3 * Albumin in the last 3 months <35g/L * Prothrombin index in the last 3 months < 70% * Hepatic comorbidity: HBV infection (defined by positive Ag HBS), HCV infection (defined by positive HCV RNA), alcohol abuse (defined by alcohol intake > 30g/day), metabolic dysfunction associated steatohepatitis, primary biliary cholangitis, Hemochromatosis, Wilson disease, α1-antitrypsin deficiency, celiac disease * History of acute cholangitis in the last 3 months prior to inclusion or current acute cholangitis * HIV infection * Prior liver transplantation * Endoscopic treatment for bile duct stenosis ≤ 3 months prior to inclusion or planned within 3 months post randomization date * History of or established or suspected hepatobiliary carcinoma. * Any severe comorbidity that may reduce life expectancy * History of malignancy diagnosed or treated within 2 years (recent localized treatment of squamous or non-invasive basal skin cancers is permitted; cervical carcinoma in situ is allowed if appropriately treated prior to inclusion) * Dosage changes of treatment for liver disease in the last 3 months or new treatment for liver disease started in the last 3 months * History of colorectal carcinoma or high-grade dypsplasia in previous screening colonoscopy * History of total colectomy * Current active IBD defined by a partial Mayo score > 2 in patients with ulcerative colitis (UC), unclassed colitis or a Crohn's Disease Activity Index (CDAI) > 150 in patients with Crohn's disease * Changes in IBD treatment or initiation of a new treatment for IBD in the last 3 months * Current treatment with biologics (anti-TNF agent, vedolizumab, ustekinumab) or JAK inhibitors (tofacitinnib) or prednisone > 10 mg/day or budesonide > 3 mg /day) (or treatment initiated less than one month) * Any contra-indication to swallow capsules * Renal insufficiency (clearance<60 ml/min) * Unable to consent, subject to legal or administrative decision (protection measure or deprivation of liberty) or involuntary psychiatric care. * Participation in another interventional research without prior consultation with the investigator responsible for the patient's monitoring in the present study (participation in other non-interventional studies is permitted) * Pregnancy or desire for pregnancy or breastfeeding Randomization criteria * No pregnancy (or desire for in the next year) * No other hepatic pathology: HBV (positive HBs Ag), HCV (positive HCV antibody and positive PCR), autoimmune hepatitis * No HIV infection (positive serology HIV1+2 antibodies) * No documented Clostridium difficile infection at inclusion or < 10 days preceding randomization (in case of infection discovered at inclusion) * No treatment with antibiotics, antifungics or probiotics < 4 weeks. * Available FMT with EBV and CMV compatibility
Locations (1)
| Site | City | Country | Site status |
|---|---|---|---|
| Hepatology Department, Saint Antoine Hospital | Paris | France |
For contacts at each site, use the official record.
Information only, not medical advice. Talk to your doctor and the trial team before making any decision about a clinical trial.