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Completed Phase 3 Interventional Accepts healthy volunteers

Comparison of Raloxifene and Lasofoxifene - A Randomized, Blinded Study of These Drugs and Placebo on Bone Loss

ClinicalTrials.gov ID: NCT00163137

Public ClinicalTrials.gov record NCT00163137. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 2, 2026, 4:55 PM EST

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Double-Blind Placebo-Controlled Trial Of The Safety, Toleration and Efficacy Of Lasofoxifene 0.25 Mg/D and Raloxifene 60Mg/D For The Prevention Of Bone Loss In Postmenopausal Women

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To compare the effects of 2 years of lasofoxifene treatment with 2 years of raloxifene 60 mg/day use and 2 years of placebo use on bone mineral density (BMD) of the lumbar spine.

Study identification

NCT ID
NCT00163137
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ligand Pharmaceuticals
Industry
Enrollment
540 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
48 Years to 75 Years
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 2003 (Type not available)
Primary completion
Oct 2005 (Actual)
Completion
Oct 2005 (Actual)
Last update posted
Aug 12, 2011

2003 – 2005

United States locations

U.S. sites
72
U.S. states
20
U.S. cities
52
Facility City State ZIP Site status
Pfizer Investigational Site Albany California 94706 —
Pfizer Investigational Site Berkeley California 94705 —
Pfizer Investigational Site La Jolla California 92037 —
Pfizer Investigational Site La Jolla California 92093-0659 —
Pfizer Investigational Site Oakland California 94609 —
Pfizer Investigational Site Oakland California 94612 —
Pfizer Investigational Site Palo Alto California 94304 —
Pfizer Investigational Site Poway California 92064 —
Pfizer Investigational Site San Diego California 92103 —
Pfizer Investigational Site San Diego California 92123 —
Pfizer Investigational Site San Diego California 92128 —
Pfizer Investigational Site Newark Delaware 19713-2094 —
Pfizer Investigational Site Brandon Florida 33511-5964 —
Pfizer Investigational Site Gainesville Florida 32605 —
Pfizer Investigational Site Gainesville Florida 32607 —
Pfizer Investigational Site Key Largo Florida 33037 —
Pfizer Investigational Site Lake Worth Florida 33461 —
Pfizer Investigational Site Leesburg Florida 34748 —
Pfizer Investigational Site Miami Florida 33143 —
Pfizer Investigational Site Miami Florida 33173 —
Pfizer Investigational Site Miami Florida 33176 —
Pfizer Investigational Site Tampa Florida 33607 —
Pfizer Investigational Site Tampa Florida 33613-3946 —
Pfizer Investigational Site Tampa Florida 33614-7118 —
Pfizer Investigational Site West Palm Beach Florida 33407 —
Pfizer Investigational Site Atlanta Georgia 30308 —
Pfizer Investigational Site Chicago Illinois 60610 —
Pfizer Investigational Site Des Moines Iowa 50309 —
Pfizer Investigational Site Wichita Kansas 67207 —
Pfizer Investigational Site Portland Maine 04102 —
Pfizer Investigational Site Bethesda Maryland 20817 —
Pfizer Investigational Site Gaithersberg Maryland 20886 —
Pfizer Investigational Site Detroit Michigan 48201 —
Pfizer Investigational Site Detroit Michigan 48236 —
Pfizer Investigational Site Southfield Michigan 48034 —
Pfizer Investigational Site Arden Hills Minnesota 55112 —
Pfizer Investigational Site Minneapolis Minnesota 55415-1226 —
Pfizer Investigational Site Albuquerque New Mexico 87102 —
Pfizer Investigational Site Albuquerque New Mexico 87106 —
Pfizer Investigational Site Akron Ohio 44312-1647 —
Pfizer Investigational Site Akron Ohio 44314 —
Pfizer Investigational Site Cleveland Ohio 44195 —
Pfizer Investigational Site Portland Oregon 97213 —
Pfizer Investigational Site Portland Oregon 97220 —
Pfizer Investigational Site Monessen Pennsylvania 15062 —
Pfizer Investigational Site Mosessen Pennsylvania 15062 —
Pfizer Investigational Site Pittsburgh Pennsylvania 15213 —
Pfizer Investigational Site West Reading Pennsylvania 19611 —
Pfizer Investigational Site Wyomissing Pennsylvania 19610-2132 —
Pfizer Investigational Site Wyomissing Pennsylvania 19610 —
Pfizer Investigational Site Chattanooga Tennessee 37403 —
Pfizer Investigational Site Chattanooga Tennessee 37412 —
Pfizer Investigational Site Cordova Tennessee 38018 —
Pfizer Investigational Site Germantown Tennessee 38138 —
Pfizer Investigational Site Memphis Tennessee 38119 —
Pfizer Investigational Site Nashville Tennessee 37203 —
Pfizer Investigational Site Dallas Texas 75230 —
Pfizer Investigational Site American Fork Utah 84003 —
Pfizer Investigational Site Pleasant Grove Utah 84062 —
Pfizer Investigational Site Provo Utah 84064 —
Pfizer Investigational Site Salt Lake City Utah 84102 —
Pfizer Investigational Site West Jordan Utah 84088 —
Pfizer Investigational Site Chesapeake Virginia 23320 —
Pfizer Investigational Site Norfolk Virginia 23502 —
Pfizer Investigational Site Richmond Virginia 23221 —
Pfizer Investigational Site Richmond Virginia 23225 —
Pfizer Investigational Site Richmond Virginia 23229 —
Pfizer Investigational Site Richmond Virginia 23294 —
Pfizer Investigational Site Richmond Virginia 23454 —
Pfizer Investigational Site Virginia Beach Virginia 23454 —
Pfizer Investigational Site Seattle Washington 98104 —
Pfizer Investigational Site Seattle Washington 98144 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00163137, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 12, 2011 · Synced Nov 2, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00163137 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →