Overview

Extension Study to Assess the Long-Term Safety of Tegaserod in Women With Symptoms of Dyspepsia

Status:
Completed
Trial end date:
2006-08-01
Target enrollment:
Participant gender:
Summary
This study is being done to evaluate the long-term safety of tegaserod in women with symptoms of dyspepsia who have completed the core study. Tegaserod will be evaluated at 6 mg twice daily.
Phase:
Phase 3
Details
Lead Sponsor:
Novartis
Treatments:
Tegaserod