drugset / Trial / NCT00287170

Efficacy Study of Targeted, Local Delivery of Drugs to Treat Crohn's Disease

NCT00287170

Phase 1/2 Completed 15 enrolled Teva GTC
RandomizedParallel-groupOpen-labelTreatment

Summary

The study is being undertaken to evaluate whether delayed-release medications, designed to begin to open in the lower intestinal tract, the main site of Crohn's Disease, are more effective than standard systemically delivered drugs to promote remission or response in CD patients. It is hypothesized that the delayed-release medications will go right to the injured tissue and heal the disease more quickly. The delayed-release test drugs are 6-mercaptopurine (at a dose of 40 mg daily) or calcitriol (at a dose of 5 mcg three times a week) versus Purinethol (6-MP at a dose of 1-2 mg/kg body weight daily). Calcitriol is a synthetically manufactured replica of a natural substance in the body that is derived from Vitamin D. There is much medical evidence that shows that lack of Vitamin D can be a possible risk factor in developing autoimmune disorders, including Crohn's Disease. Moreover, calcitriol has been shown in animal models to improve the symptoms of Crohn's Disease.

Timeline

Start
2006-07
Primary completion
Completion
2007-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Calcitriol Small molecule 5 ug Oral
Subject MERCAPTOPURINE ANHYDROUS Small molecule 1 mg/kg Oral
Subject MERCAPTOPURINE ANHYDROUS Small molecule 2 mg/kg Oral
Subject MERCAPTOPURINE ANHYDROUS Small molecule 40 mg Oral

Indications