Microbiota Transfer Therapy for Children and Adults With Both Pitt Hopkins Syndrome and Gastrointestinal Disorders: MTP-101 P

Status: Recruiting
Location: See location...
Intervention Type: Combination product
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The investigators propose to investigate Microbiota Transfer Therapy (MTT) for treating patients with Pitt-Hopkins Syndrome (PTHS) and gastrointestinal problems (constipation, bloating, abdominal pain). MTT involves a combination of 10 days of oral vancomycin (an antibiotic to kill pathogenic bacteria), followed by 1 day of bowel cleanse using magnesium citrate, followed by 4 days of high dose MTP-101P with an antacid, followed by 12 weeks of a lower maintenance dose of MTP-101P with an antacid.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 5
Maximum Age: 55
Healthy Volunteers: f
View:

• Children ages 5 to \<18 years and adults ages 18 to \< 55 years with Pitt Hopkins Syndrome (verified by genetic testing)

• GI disorder as defined below that has lasted for at least 2 years.

• No changes in medications, supplements, diet, or therapies in the 2 months prior to start of treatment, and no intention to change treatments during Part 1 (all participants) and Part 2 (group B) of the clinical trial. The only exception is GI medications, which may be reduced if symptoms reduce, and any changes during the study will be documented.

• Review of last year of medical records by the study physician.

• At least two previous trials of standard of care GI treatments that did not alleviate GI symptoms (constipation, diarrhea, bloating, gas, reflux, and/or abdominal pain). Standard of care treatments include laxatives, stool softeners, enemas, suppositories, or similar medications.

Locations
United States
Arizona
Autism/Asperger's Research Group at Arizona State University
RECRUITING
Tempe
Contact Information
Primary
James B Adams
jim.adams@asu.edu
4809653316
Backup
Jasmine K Kirby
jkkirby1@asu.edu
4802343767
Time Frame
Start Date: 2024-02-27
Estimated Completion Date: 2025-05
Participants
Target number of participants: 20
Treatments
Experimental: Group A: Treatment
Part 1: Blinded Treatment (14 weeks)~Vancomycin, Magnesium Citrate, Antacid, MTP-101P
Placebo_comparator: Group B: Placebo
Part 1: Blinded Placebo (14 weeks)~Placebo Vancomycin, Real Magnesium Citrate, Real Antacid, Placebo MTP-101P
Related Therapeutic Areas
Sponsors
Leads: Gut-Brain-Axis Therapeutics Inc.
Collaborators: Pitt Hopkins Research Foundation

This content was sourced from clinicaltrials.gov

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