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RecruitingLast updated:19 October 2020

WinPro: This phase II trial is evaluating a combination of hormone treatments that may be useful for pre-surgery breast cancer treatmentAn open-label, randomized, window of opportunity study between diagnosis and definite surgery, to assess the effect of antiestrogen therapies, alone and in combination with microionized progesterone (prometrium) in patients with newly diagnosed ER+PR+ breast cancer

Clinical summary

Summary

Eligible patients will be randomised to one of three groups. Group 1 patients will receive letrozole and promethium; patients in Group 2 will receive tamoxifen and promethium; and Group 3 will receive letrozole alone. All assigned treatments will be administered daily for two weeks prior to surgery.

Age

People18+

Phase

II

Trial Acronym

WinPro

More information

Trial Identifiers

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Commercial Sponsor

Cancer Council of NSW & St Vincent's Hospital, Sydney

Scientific Title

An open-label, randomized, window of opportunity study between diagnosis and definite surgery, to assess the effect of antiestrogen therapies, alone and in combination with microionized progesterone (prometrium) in patients with newly diagnosed ER+PR+ breast cancer

Eligibility

Inclusion

  • You have been diagnosed with a prior or secondary type of cancer.
  • You have had certain treatments, surgical procedures or drugs.

Exclusion

  • Your cancer has not spread to other parts of the body.
Message

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