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Clinical Trial Summary

This is a feasibility study which will evaluate the effects of pre-operative treatment of DCIS of the breast with palbociclib. Patients with biopsy-proven DCIS are eligible for the study. There will be 2 independent and unrelated study groups of 12 patients each, for a total of 24 patients: 1. Group A, of male or female patients treated with palbociclib single agent (n=12); 2. Group B, untreated, of male or female patients who consented translational studies in blood, as well as diagnostic and definitive surgical specimen, but not the pre-operative treatment with palbociclib (n=12).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Carcinoma, Intraductal, Noninfiltrating
  • DCIS

NCT number NCT03535506
Study type Interventional
Source Georgetown University
Contact
Status Terminated
Phase Phase 2
Start date October 8, 2018
Completion date December 6, 2023

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