Trial of H3B-6545, in Women With Locally Advanced or Metastatic Estrogen Receptor-positive, HER2 Negative Breast Cancer
Status: | Recruiting |
---|---|
Conditions: | Breast Cancer, Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/1/2019 |
Start Date: | August 17, 2017 |
End Date: | December 1, 2019 |
Contact: | Eisai Medical Information |
Email: | esi_oncmedinfo@eisai.com |
Phone: | 1-888-274-2378 |
A Phase I-II Multicenter, Open Label Trial of H3B-6545, a Covalent Antagonist of Estrogen Receptor Alpha, in Women With Locally Advanced or Metastatic Estrogen Receptor-positive, HER2 Negative Breast Cancer
The purpose of phase 1 is to determine safety, tolerability and pharmacokinetics (PK) of
H3B-6545 in women with locally advanced or metastatic estrogen receptor-positive, human
epidermal growth factor 2 (HER2)-negative breast cancer.
The purpose of phase 2 is to estimate the efficacy of H3B-6545 in terms of response rate,
duration of response (DoR), disease control rate (DCR), progression-free survival (PFS), and
overall survival (OS).
H3B-6545 in women with locally advanced or metastatic estrogen receptor-positive, human
epidermal growth factor 2 (HER2)-negative breast cancer.
The purpose of phase 2 is to estimate the efficacy of H3B-6545 in terms of response rate,
duration of response (DoR), disease control rate (DCR), progression-free survival (PFS), and
overall survival (OS).
Inclusion Criteria:
1. Pre- or post-menopausal women.
2. ER-positive, HER2-negative breast cancer that is advanced or metastatic.
3. Progressed on prior therapy. Multiple prior lines of therapy allowed in Phase 1 and 2.
4. Must be willing to undergo a biopsy prior to treatment and on Cycle 2 Day 1.
5. Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1.
6. Adequate bone marrow and organ function.
Exclusion Criteria:
1. Participant with bone-only disease (Phase I only). Note: Phase II subjects may have
predominantly lytic bone only disease.
2. Participant with inflammatory breast cancer.
3. Participant has received more than one prior chemotherapy regimen for metastatic
disease (Phase II only).
4. Females of childbearing potential who are unable or unwilling to follow adequate
contraceptive measures.
We found this trial at
4
sites
Tennessee Oncology, PLLC Since 1976 Tennessee Oncology has been providing quality cancer care. In 2013,...
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Univ of North Carolina Carolina’s vibrant people and programs attest to the University’s long-standing place...
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