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

Completed · Not applicable · Has a placebo group

Conditions studied: Ulcerative Colitis

In brief

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.

Key facts

Study ID

NCT01433471

Run by

NYU Langone Health

People needed

4

Starts

2012-08-01

Expected to finish

2015-05-01

Last updated by the study team

2016-07-01

Who can join

Age: 18 and older, up to 72. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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.
• Laboratory inclusion criteria will require a hemoglobin level of >9.0 g/dL, a white blood count between 5,000 and 15,000/μL, a platelet count of >100,000μL, a blood urea nitrogen < 40mg/dL, a serum creatinine of <2.0mg/dL, a total bilirubin < 2.5 mg/dL, and an alkaline phosphatase of <250U/dL.
• 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.

You may not qualify if…

• 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.

Where it is running

• New York University School of Medicine — New York, New York, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.