Clinical trial

Verification Study on Lafutidine in Mild Reflux Oesophagitis - Double Blind…

NCT00229424 · Taiho Pharmaceutical Co., Ltd., Industry · Completed

Key facts

NCT number NCT00229424
Title Verification Study on Lafutidine in Mild Reflux Oesophagitis - Double Blind Controlled Study With Famotidine -
Official title Verification Study on Lafutidine in Mild Reflux Oesophagitis - Double Blind Controlled Study With Famotidine -
Lead sponsor Taiho Pharmaceutical Co., Ltd., Industry
Collaborators UCB Pharma Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Gastroesophageal Reflux
Intervention type Drug, Other
Interventions Lafutidine, Famotidine, Placebo
Enrollment 325
Start date Apr 1, 2005
Primary completion Oct 1, 2006
Completion Jan 1, 2007
First posted Sep 29, 2005
Last update posted Jul 7, 2011
Countries Japan

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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