Clinical trial

PRELUDE:Study to Investigate the Prevention of Relapse in Lymphoma Using Daily…

NCT00332202 · Eli Lilly and Company, Industry · Completed

Key facts

NCT number NCT00332202
Title PRELUDE:Study to Investigate the Prevention of Relapse in Lymphoma Using Daily Enzastaurin
Official title A Phase 3 Clinical Study to Investigate the Prevention of Relapse in Lymphoma Using Daily Enzastaurin
Lead sponsor Eli Lilly and Company, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Non Hodgkin Lymphoma
Intervention type Drug
Interventions enzastaurin, placebo
Enrollment 758
Start date Jun 1, 2006
Primary completion Apr 1, 2013
Completion Jul 1, 2013
First posted Jun 1, 2006
Last update posted Sep 10, 2018
Countries Australia, Belgium, Brazil, Canada, China, Czechia, Denmark, Finland, France, Germany, Greece, Hungary and 13 more

At a glance

  • 100–999 Study sites
  • Yes 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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