Viewing Study NCT00960934


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Study NCT ID: NCT00960934
Status: TERMINATED
Last Update Posted: 2015-02-18
First Post: 2009-08-17
Is Gene Therapy: True
Has Adverse Events: True

Brief Title: A Dose-Ranging Study of MK-5442 in Postmenopausal Women With Osteoporosis (MK-5442-001)
Sponsor: Merck Sharp & Dohme LLC
Organization:

Study Overview

Official Title: A Phase IIb, Randomized, Placebo-Controlled, Dose-Ranging Study of MK-5442 in the Treatment of Postmenopausal Women With Osteoporosis
Status: TERMINATED
Status Verified Date: 2015-02
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: The purpose of this study was to identify an appropriate dose of

MK-5442 that produced an osteoanabolic effect without causing hypercalcemia in postmenopausal women with osteoporosis.
Detailed Description: Amendment 4 of the protocol changed the duration of the study from 2 years to 6 months.

Study Oversight

Has Oversight DMC: False
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?:

Secondary ID Infos

Secondary ID Type Domain Link View
2009-012926-35 EUDRACT_NUMBER None View