Breast Cancer Clinical Trial
GRN1005 Alone or in Combination With Trastuzumab in Breast Cancer Patients With Brain Metastases
Summary
The purpose of this study is to assess the efficacy, safety, and tolerability of GRN1005 in patients with brain metastases from breast cancer. For patients with HER2 positive metastatic breast cancer, GRN1005 will be assessed in combination with Trastuzumab (Herceptin®) as per standard-of-care practice.
In addition, this study will evaluate the ability of 18F-FLT to determine if the amount of change in the uptake in the brain metastases from breast cancer after GRN1005 treatment, correlates with intra-cranial response (for patients enrolled at NCI).
Full Description
Please see Brief Summary section.
Eligibility Criteria
Key Inclusion Criteria:
Age ≥ 18 years
Histologically or cytologically-documented breast cancer (HER2 status and ER/PgR status must be known)
Brain metastasis from breast cancer with or without prior WBRT
At least one radiologically-confirmed and measurable metastatic brain lesion (≥ 1.0 cm in the longest diameter) by Gd-MRI of the brain < 14 days prior to first dose (Metastatic brain lesions previously treated with SRS may not be target or non-target lesions)
Patients must be neurologically stable: On stable doses of corticosteroids and anticonvulsants (not EIAEDs, including phenytoin, phenobarbitol, carbamazepine, fosphenytoin, primidone, oxcarbazepine) for ≥ 5 days prior to obtaining the baseline Gd-MRI of the brain and ≥ 5 days prior to first dose
KPS ≥ 70%
Completed WBRT for intra-cranial lesions ≥ 28 days prior to first dose
Key Exclusion Criteria:
NCI CTCAE v4.0 Grade ≥ 2 neuropathy
CNS disease requiring immediate neurosurgical intervention (e.g., resection, shunt placement, etc.)
Known leptomeningeal disease
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There are 2 Locations for this study
Harvey Illinois, 60426, United States
Rockville Maryland, 20892, United States
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