Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
260

Summary

Conditions
  • Dyslipidemias
  • Hyperlipidemias
  • Hyperlipoproteinemias
Type
Interventional
Phase
Phase 2
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Triple (Participant, Care Provider, Investigator)Primary Purpose: Treatment

Participation Requirements

Age
Between 40 years and 125 years
Gender
Both males and females

Description

This study is intended to enable selection of a dose(s) for future development of vupanorsen for cardiovascular (CV) risk reduction and hypertriglyceridemia.

This study is intended to enable selection of a dose(s) for future development of vupanorsen for cardiovascular (CV) risk reduction and hypertriglyceridemia.

Tracking Information

NCT #
NCT04516291
Collaborators
TIMI Study Group
Investigators
Study Director: Pfizer CT.gov Call Center Pfizer