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C-Control: Efficacy and Safety of Therapy With Rosuvastatin in Statin-Naive and in Statin-Switched Patients

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

Hypercholesteremia

Study type

Observational

Funder types

Industry

Identifiers

NCT00688454
NIS-CCH-CRE-2007/1

Details and patient eligibility

About

The study explores efficacy and safety of the lipid-lowering therapy with CRESTOR in statin-naive patients and in patients with previously unsuccessful statin therapy. This study was designed to investigate the dynamic of the lipid parameters and therapy tolerability during 8-10 weeks treatment with CRESTOR

Enrollment

3,392 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with hypercholesteremia who was never treated with statins before
  • Patient with hypercholesteremia who was treated with a statin (other then rosuvastatin) but because of its adverse effects/insufficient action was switched to therapy with CRESTOR

Exclusion criteria

  • None

Trial design

3,392 participants in 1 patient group

Pt with hypercholesteremia
Description:
Patients treated with CRESTOR because of hypercholesteremia

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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