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Oral FMT (Fecal Microbial Transplant) in Subjects With Multiple Sclerosis

28 settembre 2026 aggiornato da: Griffin Hospital

A Pilot Study of Oral FMT (Fecal Microbial Transplant) in Subjects With Multiple Sclerosis

The goal of this pilot study is to determine whether fecal microbial transplant (FMT) has the potential to be an effective, safe and tolerable therapy for the treatment of multiple sclerosis (MS). The investigators plan to gather preliminary data in a small cohort of 10 to 15 adults with MS.

Panoramica dello studio

Stato

Completato

Condizioni

Descrizione dettagliata

The specific aims are to:

  1. Determine the tolerability of a single dose of 30 capsules in a group of adults with MS
  2. Determine whether any unexpected outcomes arise in participants who successfully complete an FMT procedure consisting of a single dose of 30 capsules
  3. Determine whether successfully completed FMT leads to engraftment of donor microbiome in participants
  4. If the FMT leads to engraftment of donor microbiome in participants, determine whether participants revert back to previous microbiome profiles, and if so, at what time point
  5. Determine whether engrafted species following the FMT, if detected, result in any changes in immune or metabolomic parameters relative to baseline
  6. Determine whether the FMT has any adverse impact, relative to baseline, on study participants' self-reported levels of fatigue, mental well-being, and health-related qualify of life
  7. Determine whether the FMT has any adverse impact, relative to baseline, on study participants' neurological status, relative to baseline

The study population will consist of adults with clinically definite MS who are currently untreated with any disease-modifying therapy or are being treated with glatiramer acetate or interferon beta. The research team will offer study participants a single FMT procedure in the form of 30 oral capsules which contain fecal material. Study participants will visit Griffin Hospital facilities 8 times. The first visit will involve a clinical screening. Of the 7 remaining visits, 6 will involve data collection and one will involve the FMT procedure.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

9

Fase

  • Prima fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Connecticut
      • Derby, Connecticut, Stati Uniti, 06418
        • Griffin Hospital

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 18 anni a 55 anni (Adulto)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  1. Diagnosis of clinically definite multiple sclerosis (CDMS) by 2017 McDonald Criteria
  2. Ages between 18 and 55 years, inclusive;
  3. Expanded Disability Status Score (EDSS) between 1.0 and 6.5.
  4. Currently untreated with any disease-modifying therapy (DMT) or currently being treated with glatiramer acetate or interferon beta.
  5. Ability to travel to Griffin Hospital for 8 visits over a 5-month period

Exclusion Criteria:

  1. Inability to give consent;

  2. Non-fluency in English;

  3. Inability to adhere to the protocol;

  4. Inability (e.g., dysphagia) to or unwillingness to swallow capsules;

  5. Active gastrointestinal infection at the time of enrollment;

  6. Use of antibiotics or corticosteroids within three months of study entry;

  7. Requiring or anticipating antibiotic use during the four weeks after study entry;

  8. MS relapse within one month of study entry;

  9. Previous use of any of the following FDA-approved disease-modifying drugs within 12 months of study entry, including natalizumab, fingolimod, siponimod, ozanimod, teriflunomide, diroximel, ocrelizumab, ofatumumab, and/or dimethyl fumarate; or any of the following off-label therapies, including rituximab and cyclophosphamide;

  10. Any previous use of the following FDA-approved DMTs, including mitoxantrone, alemtuzumab, and cladribine;

  11. IV immunoglobulin or plasma exchange within six months prior to study entry;

  12. Known or suspected toxic megacolon and/or known small bowel ileus;

  13. Major gastrointestinal surgery (e.g., significant bowel resection) within 3 months prior to enrollment (this does not include appendectomy or cholecystectomy);

  14. History of total colectomy or bariatric surgery;

  15. Concurrent intensive induction chemotherapy, radiation therapy or biological treatment for active malignancy;

  16. Anticipated life expectancy of less than six months;

  17. Concomitant other known autoimmune diseases;

  18. Concomitant pulmonary, cardiac, gastrointestinal (except as noted above) (Crohns, Colitis, inflammatory bowel, intestinal blockage), hepatic, dermatological or genitourinary disease.

  19. Moderate to severe dysphagia;

  20. History of alcohol abuse, as defined by the following criteria:

    Men: 5 or more alcoholic beverages per session or day, or 15 or more per week; Women: 4 or more alcoholic beverages per session or day, or 8 or more per week;

  21. History of illicit drug abuse, e.g., of cocaine, heroin, PCP, and/or narcotic substances;

  22. Grade 1 or greater lymphopenia, as measured at baseline/clinical screening;

  23. Liver Function Tests (LFTs) greater than 1½ times upper limits of normal, as measured at baseline/clinical screening;

  24. History of use of FMT or microbiome-based products (excluding probiotics) at any time, excluding this study;

  25. History of severe anaphylactic or anaphylactoid food allergy;

  26. History of solid organ transplantation;

  27. Risk for Cytomegalovirus (CMV) or Epstein Barr virus (EBV) associated disease (at investigator's discretion, e.g., immunocompromised and negative (immunoglobulin gamma) IgG testing for CMV or EBV);

  28. Women who are pregnant, lactating, planning to become pregnant, and/or not using an effective method of contraception (women of childbearing potential will undergo a pregnancy test, and will be excluded from the study if results are positive);

  29. Any allergies to neomycin or similar antibiotics such as amikacin (Amikin), gentamicin (Garamycin), kanamycin (Kantrex), paromomycin (Humatin, Paromycin), streptomycin, or tobramycin (Nebcin, Tobi);

  30. Any condition that would jeopardize the safety or rights of the subject, would make it unlikely for the subject to complete the study, or would confound the study results.

  31. Household contacts, including children under the age of 5 years, pregnant women, any person with an immunocompromised condition or on medications causing immunosuppression or persons 70 years or older;

  32. Failure to document a COVID-19 vaccine series at least two weeks prior to study entry.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Intervention

Fecal microbial transplant capsules

Oral fecal microbial transplant capsules

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in engraftment of donor microbiome in stool samples
Lasso di tempo: Pre-FMT and 4 time points post-FMT (3-7 days, 10-15 days, 40-45 days, 100-110 days)

Evidence of engraftment as measured by 16s rRNA microbiome sequencing

Pre-FMT and 4 time points post-FMT (3-7 days, 10-15 days, 40-45 days, 100-110 days)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in immune markers in blood samples assessed using assays of lymphocyte phenotyping and intracellular cytokines
Lasso di tempo: Pre-FMT and 2 time points post-FMT (40-45 days, 100-110 days)

Phenotyping will be performed: for T cells - TCRβ, TCRγ, CD4, CD8, CD25, CD44, CD62L, CD69, PD1, CTLA4; for B cells - B220, CD19, CD21, CD23, CD1d, CD5, IgA, IgG1, IgG2a(c), IgG2b; for DCs - CD11c, CD11b, BDCA1, CD8, CD103, CD205 and CD86. The intracellular cytokine (ICC) panel will be IL-6, IL-10, IL-12, IL-17, TNFα, and IFNγ.

Pre-FMT and 2 time points post-FMT (40-45 days, 100-110 days)
Change in neurological status using Kurtzke Functional Systems Scale (FSS)
Lasso di tempo: Pre-FMT and 4 time points post-FMT (3-7 days, 10-15 days, 40-45 days, 100-110 days)

The FSS uses a set of single-item ordinal clinical rating scales to rate levels of function in seven domains (pyramidal, cerebellar, brainstem, sensory, bowel and bladder, visual, and cerebral/mental). Each single item scale ranges from 0 to 5 or 6 (0 = "normal;" 5 or 6 represents the worst level of function; and 9 = "unknown"). For each single item scale, scores representing the highest level of function are as follows: pyramidal: 6 = "quadriplegia"; cerebellar: 5 = "unable to perform coordinated movements due to ataxia"; brainstem: 5 = "inability to swallow or speak"; sensory: 6 = "sensation essentially lost below the head"; bowel and bladder: 6 = loss of bowel and bladder function"; visual: 6 = "grade 5 plus maximal visual acuity of better eye of 20/60 or less"; cerebral/mental: 5 = "dementia or chronic brain syndrome - severe or incompetent." The ratings are used in conjunction with observations and information concerning gait and use of assistive devices to rate the EDSS.

Pre-FMT and 4 time points post-FMT (3-7 days, 10-15 days, 40-45 days, 100-110 days)
Change in neurological status using Kurtzke Expanded Disability Status Scale (EDSS)
Lasso di tempo: Pre-FMT and 4 time points post-FMT (3-7 days, 10-15 days, 40-45 days, 100-110 days)

The EDSS is an ordinal clinical rating scale ranging from 0 (normal neurological examination) to 10 (death due to MS) in half-point increments.

Pre-FMT and 4 time points post-FMT (3-7 days, 10-15 days, 40-45 days, 100-110 days)
Change in self-reported health-related quality of life assessed using the Health Status Questionnaire Short-Form 36 (SF-36)
Lasso di tempo: Pre-FMT and 3 time points post-FMT (10-15 days, 40-45 days, 100-110 days)

The SF-35 has 36 questions. It has a single item covering change in health status over the last year and 8 multi-item scales. The scoring system is relatively complex and generates 8 subscales and 2 summary scores. The 8 subscales are: physical functioning, role limitations due to physical problems, bodily pain, general health perceptions, vitality, social functioning, role-limitations due to emotional problems, and mental health. Two summary scales (Physical and Mental) have been derived using factor analytic methods. Scales are set up so that a higher score indicates better health. To achieve this, responses on 10 items are recoded before being added to other items on the same scale. Raw scale scores are then transformed to a 0-100 scale.

Pre-FMT and 3 time points post-FMT (10-15 days, 40-45 days, 100-110 days)
Change in self-reported mental health status assessed using Mental Health Inventory (MHI)
Lasso di tempo: Pre-FMT and 3 time points post-FMT (10-15 days, 40-45 days, 100-110 days)

The MHI consists of 18 items and assesses several domains of mental health. The scoring system generates 4 subscale scores (Anxiety, Depression, Behavioral Control, and Positive Affect) and 1 total score. The subscale and total scores range from 0-100, with higher scores indicating better mental health.

Pre-FMT and 3 time points post-FMT (10-15 days, 40-45 days, 100-110 days)
Change in self-reported levels of fatigue assessed using Modified Fatigue Impact Scale (MFIS)
Lasso di tempo: Pre-FMT and 3 time points post-FMT (10-15 days, 40-45 days, 100-110 days)

The MFIS provides an assessment of the effects of fatigue on physical, cognitive, and psychosocial function. It consists of 21 items. The items be aggregated into 3 subscales (Physical, Cognitive, and Psychosocial), as well as into a total MFIS score. All items are scaled so that higher scores indicate a greater impact of fatigue on a patient's activities. The physical subscale can range from 0-36. The cognitive subscale can range from 0-40. The psychosocialsub scale can range from 0-8. The Total MFIS score can range from 0-84.

Pre-FMT and 3 time points post-FMT (10-15 days, 40-45 days, 100-110 days)
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]
Lasso di tempo: Day of FMT procedure and 5 time points post-FMT (1 day, 3-7 days, 10-15 days, 40-45 days, 100-110 days), or any time the study team is contacted by subjects who report adverse side effects

Measured by subject's ability to consume capsules as directed without vomiting or adverse side effects (as opposed to mild side effects)

Day of FMT procedure and 5 time points post-FMT (1 day, 3-7 days, 10-15 days, 40-45 days, 100-110 days), or any time the study team is contacted by subjects who report adverse side effects

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Joseph B Guarnaccia, MD, Griffin Hospital
  • Investigatore principale: Frederick Browne, MD, Griffin Hospital

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

28 ottobre 2019

Completamento primario (Effettivo)

21 dicembre 2024

Completamento dello studio (Effettivo)

30 dicembre 2024

Date di iscrizione allo studio

Primo inviato

7 agosto 2019

Primo inviato che soddisfa i criteri di controllo qualità

18 settembre 2019

Primo Inserito (Effettivo)

19 settembre 2019

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

1 ottobre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

28 settembre 2026

Ultimo verificato

1 settembre 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Sì

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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