Viewing Study NCT00092027



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Last Modification Date: 2024-10-26 @ 9:10 AM
Study NCT ID: NCT00092027
Status: COMPLETED
Last Update Posted: 2022-02-03
First Post: 2004-09-21

Brief Title: A Study to Evaluate the Safety and Tolerability of MK0217 in Women 0217-219
Sponsor: Organon and Co
Organization: Organon and Co

Study Overview

Official Title: A Randomized Double-Blind Multicenter Placebo-Controlled Study to Compare the Safety and Tolerability of an Oral Buffered Solution of Alendronate Sodium 70 mg Once-Weekly Versus Placebo for the Treatment of Osteoporosis in Postmenopausal Women
Status: COMPLETED
Status Verified Date: 2022-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study is to assess the safety and tolerability of MK0217 being evaluated to treat women with postmenopausal osteoporosis
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
2004_017 None None None
MK0217-219 None None None