Non-interventional Study on the Monthly Administration of 300 mg AliRocumab (PRALUENT®) With the 2 ml SYDNEY Auto-injector (MARS)

  • STATUS
    Recruiting
  • participants needed
    300
  • sponsor
    Sanofi
Updated on 7 February 2023

Summary

Primary objectives:

  • To assess the effectiveness of the PRALUENT® 2 ml SYDNEY auto-injector as measured by the lipid-lowering effect of alirocumab after approx. 12 weeks treatment
  • To assess the treatment satisfaction, as well as patient adherence and persistence after approximately 12 weeks of treatment with the PRALUENT® 2 ml SYDNEY auto-injector

Secondary objective:

Safety and tolerability

Description

Study duration per participant is approximately 12 weeks

Details
Condition Primary Hypercholesterolaemia and Mixed Dyslipidaemia, Atherosclerotic Cardiovascular Disease
Clinical Study IdentifierNCT05129241
SponsorSanofi
Last Modified on7 February 2023

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