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Clinical Trial Summary

This is a randomised, double-blind, placebo-controlled, therapeutic confirmatory multicentre trial with 4 parallel treatment groups. The design is adaptive group-sequential with two interim analyses, possible sample size re-estimation after the first or second interim analysis and drop-the-loser approach. The study design was primarily chosen to show superior efficacy of Tepilta® compared to the single components and to placebo. Evaluation of safety is a secondary objective.


Clinical Trial Description

Tepilta® Suspension is indicated for treatment of pain in the upper digestive system induced by radiation therapy, in particular for radiation-induced oesophagitis. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01336530
Study type Interventional
Source Viatris Inc.
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Status Terminated
Phase Phase 3
Start date April 2011
Completion date January 2017