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Spots Global Cancer Trial Database for Ruxolitinib for Premalignant Breast Disease

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Ruxolitinib for Premalignant Breast Disease

Official Title: TBCRC 042 - A Randomized Phase II Window-of-Opportunity Trial of Ruxolitinib in Patients With High Risk and Premalignant Breast Conditions

Study ID: NCT02928978

Study Description

Brief Summary: This study is evaluating how ruxolitinib affects premalignant breast cells. One half of the study participants will receive ruxolitinib for approximately 15 days, and the other half will receive a placebo (sugar pill) for approximately 15 days. Once study participants have completed their ruxolitinib or placebo, participants will undergo surgery to remove the premalignant breast tissue.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Alabama at Birmingham, Birmingham, Alabama, United States

Indiana University Melvin and Bren Simon Cancer Center, Indianapolis, Indiana, United States

Montefiore Medical Center, Bronx, New York, United States

University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States

Vanderbilt-Ingram Cancer Center, Nashville, Tennessee, United States

Baylor College of Medicine, Houston, Texas, United States

University of Texas MD Anderson Cancer Center, Houston, Texas, United States

Contact Details

Name: Julie Nangia, M.D.

Affiliation: Baylor College of Medicine

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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