Proof of Concept (Bone Resorption/Bone Mineral Density) Study (0429-005)

NCT00533650 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 227

Last updated 2016-07-29

No results posted yet for this study

Summary

A study to asses the safety and efficacy of MK0429 in postmenopausal women with osteoporosis.

Conditions

  • Post-Menopausal Osteoporosis

Interventions

DRUG

MK0429

Sponsors & Collaborators

Principal Investigators

  • Medical Monitor · Merck Sharp & Dohme LLC

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
50 Years
Max Age
75 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2000-12-31
Primary Completion
2002-10-31
Completion
2002-10-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00533650 on ClinicalTrials.gov