Overview

FOSAMAX PLUS and FOSAMAX PLUS D Re-examination Study (0217A-267)

Status:
Completed
Trial end date:
2010-07-01
Target enrollment:
Participant gender:
Summary
This survey is conducted for preparing application materials for re-examination under the Pharmaceutical Affairs Laws and its Enforcement Regulation, its aim is to reconfirm the clinical usefulness of FOSAMAX PLUS / FOSAMAX PLUS D through collecting the safety information according to the Re-examination Regulation for New Drugs. Note: FOSAMAX PLUS D is known as FOSAMAX PLUS in several markets. FOSAMAX PLUS (70 mg/2800 IU) and FOSAMAX PLUS D (70 mg/5600 IU).
Details
Lead Sponsor:
Merck Sharp & Dohme Corp.
Treatments:
Alendronate