CLINICAL TRIALS

MPM-SL0905 Trial

Evaluation of beneficial effects of MPM-SL0905 in comparison to placebo.

This study is completed.      

Brief Title Evaluation of beneficial effects of MPM-SL0905 in comparison to placebo.
Trial Reference TBI-00206
EUDRA CT-number 2006-006738-16
Coordinating Investigator Prof. Dr. Heiner K. Berthold
Trial centers 9 centers in Germany (German Drug Law –AMG)
Indications High cholesterol level
Trial Phase Phase II
Study Design Double-blind, placebo-controlled, randomized, parallel-groups, multi-centre clinical trial.
Outcome measure One primary end point and 12 secondary end-points
Number of patients Included patients: 152
Eligible patients: 128 (64 patients per group)
Time schedule Three months treatment per patient plus six weeks run-in phase.
Trial Timelines First patient in: August 2007
Last patient out: April 2008