Pilot Study of Fundamental Modification of the Gut Microbiota in the Treatment of Refractory Crohn's Disease (Holiday)

Children's Hospital of Philadelphia (CHOP)

Status and phase

Completed

Phase 2

Conditions

Crohn Disease

Treatments

Drug: Polyethylene Glycol 3350

Drug: Vancomycin

Drug: Neomycin

Drug: Ciprofloxacin

Drug: Fluconazole

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT03476317

17-014343

5K23DK109136-02 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The purpose of this study is to determine the effect of a novel gut microbiota-targeted therapeutic regimen (bowel lavage and antibiotics with or without an antifungal) in the management of active Crohn's Disease (CD) or indeterminate colitis (IBDU) that is refractory to conventional, immunosuppressive therapy. In addition, the study will determine the effect of PEG lavage alone on fecal calprotectin and gut microbiota in patients who are undergoing a PEG lavage for clinical care.

Full description

Investigators will evaluate the efficacy of a novel treatment regimen, employing non-immunosuppressive medications, in the management of refractory CD or IBDU. Refractory patients include those patients who have experienced loss of responsiveness (LOR) or primary nonresponse to an immunomodulator or a biologic. Investigators will treat participants with a combination of gut microbiota-targeted therapies to restore a healthy gut microbiome composition. Investigators believe that this strategy will both treat the gut inflammation associated with inflammatory bowel disease (IBD) as well as salvage response to immune suppressive therapies.

Investigators will also evaluate the effect of PEG lavage alone on fecal calprotectin and gut microbiota. Participants in this arm, will be undergoing a PEG lavage in preparation for a endoscopy for clinical care. They will be asked to provide stool samples, prior to and after their PEG lavage. Participants will not be receiving any investigational treatments.

Enrollment

10 patients

Sex

All

Ages

6+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Group 1

Inclusion Criteria:

Males or females 6-18 years of age
Current weight >10 kg (or 22 lb)
Ability to swallow pills
Normal kidney function
Normal Aspartate transaminase (AST), Alanine transaminase (ALT), and alkaline phosphatase
Active CD or IBDU defined as PCDAI ≥ 30
C-Reactive Protein (CRP) ≥ 15mg/L (or 1.5mg/dL) or fecal calprotectin (FCP)>350mcg/g (within one month of enrollment)
Have been treated with one of the following therapies for at least 8 weeks with primary nonresponse or an initial response, followed by loss of response [LOR] (self-reported worsening of symptoms for ≥ 7 days): azathioprine, 6-mercaptopurine, methotrexate, adalimumab, certolizumab, golimumab, infliximab, natalizumab, vedolizumab, or ustekinumab **These medications must have been administered at standard, therapeutic dosages.

Exclusion Criteria:

Known allergy or intolerance to aminoglycosides or any of the medications used in this study
Current use of one or more of the following medications: 5-fluorouracil, digoxin, anticoagulants, theophylline, phenytoin, probenecid, duloxetine, clozapine, sildenafil, hydrochlorothiazide, cyclosporine, hypoglycemics, terfenadine, tacrolimus, rifabutin, midazolam, and voriconazole
Known diagnosis of diabetes mellitus
Known or suspected structuring disease producing obstructive symptoms
Active Clostridium difficile infection
Prolonged QTc interval as seen on enrollment EKG
Current use of antibiotics
Starting or increasing the dose of an IBD related medication within 4 weeks of screening

Group 2

Inclusion Criteria

Males or females 10 years of age and older.
Patients undergoing a clinical GI endoscopy due to suspicion for active intestinal inflammation determined by physician global assessment (PGA).
Undergoing a bowel preparation as part of clinical care.
Parental/guardian permission (informed consent) and if appropriate, child assent.

Exclusion Criteria

Antibiotic use within the past 30 days.
Current presence of an ostomy bag.
Patients undergoing a non- polyethylene glycol 3350 cleanout.
Unwillingness to provide informed consent.
Parents/guardians or subjects who, in the opinion of the Investigator, may be non-compliant with study schedules or procedures.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

10 participants in 3 patient groups, including a placebo group

Group 1-Fluconazole

Experimental group

Description:

Vancomycin oral suspension four times daily (Day 1-14), plus neomycin orally three times daily (Days 1-3), plus ciprofloxacin orally twice daily (Day 4-14), plus Polyethylene Glycol 3350 (Miralax) dissolved in Gatorade on day 2, plus fluconazole orally once daily (Day 1-14).

Treatment:

Drug: Fluconazole

Drug: Ciprofloxacin

Drug: Neomycin

Drug: Vancomycin

Drug: Polyethylene Glycol 3350

Group 1-Placebo

Placebo Comparator group

Description:

Treatment:

Drug: Ciprofloxacin

Drug: Neomycin