ClinicalTrials.Veeva

Menu

Efficacy and Safety of Fluvastatin in Different Doses in Adults With Mixed Dyslipidemia or Primary Hypercholesterolemia

Novartis logo

Novartis

Status and phase

Completed
Phase 3

Conditions

Mixed Dyslipidemia
Hypercholesterolemia

Treatments

Drug: Fluvastatin

Study type

Interventional

Funder types

Industry

Identifiers

NCT00136799
CXUO320B2302

Details and patient eligibility

About

The purpose of the study is to evaluate the safety and tolerability of fluvastatin 80 mg in a Chinese population. This study is not recruiting patients in the US.

Enrollment

325 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Mixed dyslipidemia
  • Primary hypercholesterolemia

Exclusion criteria

  • Pregnant or lactating women
  • Age > 18 years

Other protocol-defined inclusion and exclusion criteria may apply.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems