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Ruxolitinib for Premalignant Breast Disease — TBCRC042  

Ductal Carcinoma In Situ Clinical Trial

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

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02928978
Study type Interventional
Source Baylor Breast Care Center
Contact Kristen Otte
Phone 713-798-8874
Email clinical-research@breastcenter.tmc.edu
Status Recruiting
Phase Phase 2
Start date May 13, 2018
Completion date January 2025
View Details
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