Clinical trial

A Study to Evaluate Daily Pravastatin, Fenofibrate or Pravafen in the Treatment…

NCT00459745 · Shionogi, Industry · Completed

Key facts

NCT number NCT00459745
Title A Study to Evaluate Daily Pravastatin, Fenofibrate or Pravafen in the Treatment of Combined Hyperlipidemia
Official title A Multi-Center, Prospective, Longitudinal, Randomized, Double-Blind, Phase III Study to Evaluate the Efficacy and Safety of Daily Administration of Pravastatin 40 mg or Fenofibrate 160 mg or Pravafen (the Combination of Pravastatin and Fenofibrate 40/160 mg) for 12 Weeks Followed by a 52-Week…
Lead sponsor Shionogi, Industry
Collaborators Integrium Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Combined Hyperlipidemia
Intervention type Drug
Interventions Pravafen, Pravastatin, Fenofibrate
Enrollment 481
Start date Apr 1, 2007
Primary completion Apr 1, 2008
Completion Jul 1, 2009
First posted Apr 12, 2007
Last update posted Apr 24, 2018
Countries United States

At a glance

  • 10–99 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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