Actively Recruiting

Phase 1
Age: 18Years +
FEMALE
NCT05900895

Estradiol Plus Olaparib for Breast Cancer (PHOEBE)

Led by Mary D Chamberlin · Updated on 2025-11-20

6

Participants Needed

1

Research Sites

228 weeks

Total Duration

On this page

Sponsors

M

Mary D Chamberlin

Lead Sponsor

D

Dartmouth-Hitchcock Medical Center

Collaborating Sponsor

AI-Summary

What this Trial Is About

Determine the safety and recommended Phase II dose of olaparib in combination with 17b-estradiol in post-menopausal patients with advanced ER+/HER2- breast cancer.

CONDITIONS

Official Title

Estradiol Plus Olaparib for Breast Cancer (PHOEBE)

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Post-menopausal women with ER+/HER2- breast cancer
  • Metastatic or locoregional recurrence not curable with current treatments
  • Received at least one prior endocrine-based therapy in the advanced or metastatic setting
Not Eligible

You will not qualify if you...

  • No concurrent anti-cancer therapies allowed during study except anti-resorptive bone therapies (e.g., bisphosphonates, denosumab)
  • Any investigational cancer therapy or systemic chemotherapy within the last 3 weeks
  • Any radiation therapy within the last 2 weeks
  • Known central nervous system disease unless clinically stable for 3 months or more
  • Use of strong or moderate CYP3A inhibitors
  • Persistent side effects of grade 2 or higher caused by previous cancer therapy
  • History of deep venous thrombosis, pulmonary embolism, stroke, acute myocardial infarction, or congestive heart failure
  • Previous cancer not treated with curative intent or with a recurrence risk of 30% or higher
  • Severe kidney impairment with creatinine clearance of 30 mL/min or less

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Dartmouth Cancer Center

Lebanon, New Hampshire, United States, 03756

Actively Recruiting

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Research Team

R

Research Nurse

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

1

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