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Raloxifene Hydrochloride or Placebo in Postmenopausal Women at Risk for Major Coronary Events
The purpose of this study is to determine whether raloxifene compared with placebo lowers the risk of coronary events and reduces the risk of invasive breast cancer in postmenopausal women at risk for major coronary events.
Age
55 - No limit years
Sex
FEMALE
Healthy Volunteers
No
For additonal information regarding investigative sites for this trial, please call 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559), Monday-Friday, 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST) or speak with your personal physician
Minneapolis, Minnesota, United States
Start Date
June 1, 1998
Completion Date
November 1, 2005
Last Updated
January 26, 2007
10,000
Estimated participants
raloxifene
DRUG
placebo
DRUG
Lead Sponsor
Eli Lilly and Company
NCT07191730
NCT06909773
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06505109