Mucosal Immunity of Ulcerative Colitis Patients Undergoing Therapy With Trichuris Suis Ova

NCT ID: NCT01433471

Last Updated: 2016-07-01

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 4 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-08-31
• Study Completion Date: 2015-05-31

Brief Summary

The purpose of this study is to understand the immune response activated in the human gastrointestinal tract by Trichuris Suis Ova (TSO) in patients with ulcerative colitis.

Detailed Description

The concept of helminthic therapy (using worms to treat diseases) is supported by experiments in mouse models as well as several clinical studies. TSO, which are purified eggs from the porcine whipworm Trichuris suis, are being investigated in clinical trials as a potential therapeutic agent for the treatment of active Crohn's disease, relapsing multiple sclerosis, peanut and tree nut allergy, and adults with autistic disorders.

The goal of this study is to understand the immune mechanisms activated in the human gastrointestinal tract by treatment with TSO, which may lead to improvements in the symptoms of ulcerative colitis (UC). TSO have been shown to have a clinical benefit on a subset of patients with UC in a previous randomized placebo-controlled trial (Summers et al. 2005). However, the mechanisms of action of TSO on the intestinal mucosa remain unclear.

We propose an exploratory 24-week mechanistic randomized double-blind placebo-controlled crossover study of TSO in patients with established and active UC to better characterize similarities and differences in the immune mechanisms of the intestinal mucosa in response to TSO. We hypothesize that treatment with TSO will lead to an anti-inflammatory immune response in some individuals with UC through an increase in intestinal mucus production and modulation of Th1, Th2, Th17, and T-regulatory effector lymphocyte populations.

Conditions

Ulcerative Colitis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: DOUBLE

Study Groups

Trichuris suis ova followed by placebo

Subjects in this arm will receive Trichuris suis ova for 12 weeks, followed by placebo for 12 weeks after crossover

Group Type: EXPERIMENTAL

Trichuris suis ova

Intervention Type: DRUG

2,500 eggs by mouth every two weeks for 12 weeks

Placebo followed by Trichuris Suis Ova

Subjects in this arm will receive placebo for 12 weeks, followed by Trichuris suis ova for 12 weeks after crossover

Group Type: ACTIVE_COMPARATOR

Trichuris suis ova

Intervention Type: DRUG

2,500 eggs by mouth every two weeks for 12 weeks

Interventions

Trichuris suis ova

2,500 eggs by mouth every two weeks for 12 weeks

Intervention Type: DRUG

Other Intervention Names

TSO

Eligibility Criteria

Inclusion Criteria

• Subjects will be outpatients between the ages of 18 and 72.
• Subjects must have a biopsy-proven diagnosis of ulcerative colitis for greater than three months.
• There should be evidence of active disease with a total Mayo score of 6 to 10 points (scores range from 0 to 12, with higher scores indicating more severe disease activity).
• There should be moderate (marked erythema, lack of vascular pattern, friability, erosions) to severe (spontaneous bleeding, ulceration) active disease on colonoscopy (Mayo endoscopic score of at least 2) at time of enrollment.
• Women will be required to have a negative urine pregnancy test and to practice birth control.
• The following medications will be allowed and continued throughout the study: Oral or rectal sulfasalazine, mesalamine, or mesalamine derivative (maintenance therapy of > 8 weeks, stable dose of > 4 weeks); Oral corticosteroid (prednisone, prednisolone, or budesonide) at an equivalent dose of a maximum of 40mg daily prednisone (maintenance therapy of >4 weeks, stable dose of > 2 weeks), azathioprine or 6-mercaptopurine (maintenance therapy of > 8 weeks, stable dose of > 4 weeks).
• Subjects must have the ability to provide informed consent and be willing to keep all scheduled appointments for the duration for the study period.

Exclusion Criteria

• Inpatients, pregnant patients, patients with impaired cognition, patients with a history of active substance abuse in the past six months, and children.
• Patients with a history of bowel surgery in the prior six months or who currently or previously had an ileostomy or colostomy.
• Patients with active malignancy or treatment with anticancer drugs in the past 5 years, have a history of colorectal cancer or dysplasia, or a history of neoplasm of the gastrointestinal tract.
• Female patients who are pregnant, breastfeeding, wishing to become pregnant during study participation, or unwilling to use birth control.
• Patients with white blood count <5,000 or >15,000/mm3; platelet count <150,000 per μl; or iron or vitamin B12 deficiency. Correction of lab exclusion is allowed provided that medical condition is not deemed to put patient at risk and stability of result is sustained for a minimum of 30 days.
• Patients with stools positive for enteric pathogens, ova, or parasites at Screening
• Patients with active hepatitis B virus or hepatitis C virus infection or have been exposed to human immunodeficiency virus (HIV).
• Patients who have received an anti-tumor necrosis factor inhibitor (e.g. infliximab) within 12 weeks prior to Screening
• Patients who have received antibiotic, antifungal or antiparasitic medication in the last 2 weeks prior to Screening and/or would potentially require this during the study treatment period.
• Patients with evidence of poor compliance with medical advice and instruction including diet or medication.
• Patients who are unable or unwilling to swallow study medication suspension.
• Patients will be excluded if they have previously attempted helminthic therapy.
• There must not be evidence of fulminant colitis or a Mayo score of greater than 10
• Patients will be excluded if other clinically significant disease is present that could interfere with protocol compliance or interpretation of the results.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 72 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

NYU Langone Health

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Michael A Poles, M.D., Ph.D.

Role: PRINCIPAL_INVESTIGATOR

NYU Langone Health

P'ng Loke, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

NYU Langone Health

Martin J Wolff, M.D.

Role: STUDY_DIRECTOR

NYU Langone Health

Locations

New York University School of Medicine

New York, New York, United States

Countries

United States

Other Identifiers

R#11-02470

Identifier Type: -

Identifier Source: org_study_id