Evaluation of Revaree Plus in Women With Breast Cancer

Status: Recruiting
Location: See all (7) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

The purpose of this study is to find out whether Revaree Plus is effective at improving vaginal health for people who are having symptoms of vaginal dryness during breast cancer treatment.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• ≥18 years of age at the time of signing informed consent.

• Stage 0-3 hormone-receptor positive breast cancer confirmed at MSKCC

• Able to complete study questionnaires in English or Spanish

• Breast cancer patients must have completed chemotherapy or radiation therapy (and can be on maintenance therapy)

• Currently on an aromatase inhibitor or tamoxifen

• Currently have no clinical evidence of disease

• Reporting being bothered by vaginal symptoms of estrogen deprivation (i.e., vaginal dryness, dyspareunia, or discomfort \[pain with intercourse or examination\])

• A total score of 4 or greater in VAS

• Without history of other cancers (excluding non-melanoma skin cancer)

• Must sign an informed consent indicating that the participant understands the purpose of, and procedures required for the study and is willing to participate in the study

Locations
United States
New Jersey
Memorial Sloan Kettering Basking Ridge (Consent Only)
RECRUITING
Basking Ridge
Memorial Sloan Kettering Monmouth (Consent Only)
RECRUITING
Middletown
Memorial Sloan Kettering Bergen (Consent Only)
RECRUITING
Montvale
New York
Memorial Sloan Kettering Cancer Center Suffolk-Commack (Consent Only)
RECRUITING
Commack
Memorial Sloan Kettering Westchester (Consent Only)
RECRUITING
Harrison
Memorial Sloan Kettering Cancer Center
RECRUITING
New York
Memorial Sloan Kettering Nassau (Consent Only)
RECRUITING
Uniondale
Contact Information
Primary
Shari Goldfarb, MD
goldfars@mskcc.org
646-888-5080
Backup
Jeanne Carter, PhD
carterj@mskcc.org
646-888-5076
Time Frame
Start Date: 2025-06-20
Estimated Completion Date: 2029-06-20
Participants
Target number of participants: 60
Treatments
Experimental: Hormone-receptor positive breast cancer participants
Participants will have a diagnosis of Stage 0-III Hormone-receptor positive breast cancer
Related Therapeutic Areas
Sponsors
Leads: Memorial Sloan Kettering Cancer Center

This content was sourced from clinicaltrials.gov