Overview

Cozaar XQ Re-examination Study (MK-0954-349)

Status:
Completed
Trial end date:
2015-03-01
Target enrollment:
0
Participant gender:
All
Summary
This survey is conducted for preparing application material for re-examination under the Pharmaceutical Affairs Law and its Enforcement Regulation; its aim is to reconfirm the clinical usefulness of COZAAR XQ through collecting the safety and efficacy information according to the Re-examination Regulation for New Drugs.
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Merck Sharp & Dohme Corp.
Treatments:
Amlodipine
Losartan
Criteria
Inclusion criteria:

- Participant with essential hypertension

- Participant who is treated with COZAAR XQ within local label for the first time

Exclusion criteria:

- Participant who is treated with COZAAR XQ before contract and out of enrollment period

- Participant who has a contraindication to COZAAR XQ according to the local label