ClinicalTrials.gov
ClinicalTrials.gov Menu

Pilot Study of the Effect of Duavee® on Benign Breast Tissue Proliferation

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT02729701
Recruitment Status : Recruiting
First Posted : April 6, 2016
Last Update Posted : January 17, 2018
Sponsor:
Collaborator:
Pfizer
Information provided by (Responsible Party):
Carol Fabian, MD, University of Kansas Medical Center

Brief Summary:
The purpose of this study is to learn whether daily use of Duavee® is accepted and tolerated by peri- and post-menopausal women at moderate risk for development of breast cancer.

Condition or disease Intervention/treatment Phase
Breast Cancer Drug: Duavee Phase 2

Detailed Description:
Duavee® is tissue specific estrogen complex of bazedoxifene plus conjugated estrogen which is FDA approved for relief of menopausal symptoms and prevention of osteoporosis in women with a uterus who have not been diagnosed with estrogen dependent neoplasia. The overall purpose of this research is to demonstrate in a preliminary fashion that despite reduction in menopausal symptoms, (Duavee®) does not increase and may decrease proliferation in benign breast tissue in a cohort of peri- or post-menopausal women at moderately increased risk for breast cancer. If this pilot shows rapid accrual, good retention, and lack of significant increase in the risk biomarker Ki-67 in benign breast tissue, a larger prevention trial is envisioned

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 40 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Pilot Study of the Effect of Duavee® on Benign Breast Tissue Proliferation in Peri or Post-menopausal Women at Moderate Risk for Development of Breast Cancer
Study Start Date : April 2016
Estimated Primary Completion Date : March 2019
Estimated Study Completion Date : May 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Breast Cancer

Arm Intervention/treatment
Experimental: Duavee
Participants will be asked to take Duavee for 6 months while on the study.
Drug: Duavee
Once daily tablet of Duavee (Bazedoxifene (20 mg) plus conjugated estrogen (0.45 mg))
Other Name: conjugated estrogens/bazedoxifene




Primary Outcome Measures :
  1. Feasibility for a larger trial [ Time Frame: 6 Months ]
    Outcome will be based on three separate factors used collectively to determine feasibility of the study and consideration of a subsequent larger trial. These are accrual rate (ability to accrue target number of subjects in a timely manner), dropout rate (frequency of subjects who are compliant and complete the intervention) and change in Ki-67 (increase vs decrease in percent of cells stained positive in the majority of subjects). Should accrual be inadequate or too slow; or if retention is too low; then a decision would be made not to proceed to a larger trial. Also, if there is evidence of an increase in proliferation (Ki-67) then no further studies would be planned.


Secondary Outcome Measures :
  1. Change in Ki-67 [ Time Frame: Change from Baseline to Month 6 ]
    Assessment by immunocytochemistry of the percent of breast epithelial cells staining positive.

  2. Change in benign breast tissue estrogen responsive genes [ Time Frame: Change from Baseline to Month 6 ]
    Assessment by RT-qPCR of breast epithelial cells of relative rate of gene expression.

  3. Change in hormone levels [ Time Frame: Change from Baseline to Month 6 ]
    Assessment of concentrations of hormones in serum by radioimmunoassay

  4. Change in levels of Duavee in the blood [ Time Frame: Change from Baseline to Month 6 ]
    Assessment of concentration of Duavee and metabolites in plasma

  5. Change in body composition [ Time Frame: Change from Baseline to Month 6 ]
    Assessment by Dual Energy X-ray Absorptivity (DEXA)

  6. Change in breast density [ Time Frame: Change from Baseline to Month 6 ]
    Assessment of mammograms for percent of breast considered to be at increased density



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   up to 61 Years   (Child, Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Women with vasomotor symptoms with a uterus who are postmenopausal or in late menopause transition
  • Body Mass Index (BMI) <36 kg/m2
  • Class I-III mammogram within 6 months of Random Periareolar Fine Needle Aspiration (RPFNA); If Class 0 or 4, must be resolved with additional procedures
  • If previously on oral contraceptives or hormone replacement, off for 8 weeks or more prior to baseline RPFNA; the exception is low dose vaginal hormones
  • Confirmed moderate risk of developing breast cancer
  • RPFNA results within study defined range
  • Kidney and liver function within study defined range
  • Willing and able to comply with study related procedures

Exclusion Criteria:

  • Previous biopsy showing evidence of breast cancer
  • Have a predisposition to or prior history of thromboembolism, deep venous thrombosis, pulmonary embolism, or stroke
  • History of renal or liver disease
  • Prior ovarian or endometrial cancer
  • Stopped or started hormone replacement within 8 weeks
  • Any other condition or intercurrent illness that in the opinion of the investigator makes the woman a poor candidate for RPFNA
  • Currently taking or have taken specific medications in the past 6 months
  • Participation on any chemoprevention trial within 6 months
  • Current illness which would make potential participant unsuitable for enrollment

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02729701


Contacts
Contact: Bruce Kimler, PhD (913) 588-4523 bkimler@kumc.edu

Locations
United States, Kansas
University of Kansas Medical Center Recruiting
Kansas City, Kansas, United States, 66160
University of Kansas Medical Center Breast Cancer Prevention Center Recruiting
Westwood, Kansas, United States, 66208
Sponsors and Collaborators
University of Kansas Medical Center
Pfizer
Investigators
Principal Investigator: Carol Fabian, MD University of Kansas Medical Center

Responsible Party: Carol Fabian, MD, Professor, Director Breast Cancer Prevention Center, University of Kansas Medical Center
ClinicalTrials.gov Identifier: NCT02729701     History of Changes
Other Study ID Numbers: STUDY00002440
First Posted: April 6, 2016    Key Record Dates
Last Update Posted: January 17, 2018
Last Verified: January 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: Results will be published in aggregate; no individual participant data will be made available.

Additional relevant MeSH terms:
Breast Neoplasms
Neoplasms by Site
Neoplasms
Breast Diseases
Skin Diseases
Estrogens
Estrogens, Conjugated (USP)
Bazedoxifene
Hormones
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs
Selective Estrogen Receptor Modulators
Estrogen Receptor Modulators
Hormone Antagonists
Bone Density Conservation Agents