drugset / Trial / NCT01216280

Efficacy and Tolerability Study of Natura-Alpha in the Treatment of Patients With Active Ulcerative Colitis

NCT01216280 ↗

Phase 2 Unknown 75 enrolled Natrogen Therapeutics International, Inc
RandomizedParallel-groupDouble-blindTreatment

Summary

This study is to evaluate the efficacy and tolerability of multiple oral doses of Natura-alpha capsule administered to patients with active ulcerative colitis. This will be a randomized, double-blind, placebo-controlled, parallel-design study. Up to 75 patients will complete this study (20 to 25 patients per treatment group) at approximately 10-12 clinical sites in the Unites States. Patients will be assigned at a 1:1:1 ratio to receive placebo, Natura-alpha 10 mg or Natura-alpha 20 mg, b.i.d. Replacement patients may be added, pending Sponsor approval, if it appears that less than 60 patients will complete the study.

Timeline

Start
2010-07
Primary completion
2011-07
Completion
2011-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Natura-alpha Unknown 10 mg Oral
Subject Natura-alpha Unknown 20 mg Oral

Indications