Trial intelligence / Profile preview

Cevimeline for Post-Radiation Xerostomia

NCT00017511Phase 3Completed

Sponsor
Daiichi Sankyo Co., Ltd.
Start
Jun 2001
Primary completion
Mar 2003
Modality
Small Molecules
Countries
1
01

Overview

Phase 3, randomised, double-blind trial in xerostomia comparing Cevimeline with Placebo (2 arms). Primary endpoints: Dryness of the oral cavity at 12 weeks and Salivary flow at 12 weeks. Started Jun 2001; status: completed.

02

Drugs

cevimeline
03

Conditions

xerostomia

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