Clinical Trial Details
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NCT00649207 : A Phase I Study of ABT-888 in Combination With Conventional Whole Brain Radiation Therapy (WBRT) in Cancer Patients With Brain Metastases
PhasePhase 1
AgesMin: 18 Years Max: N/A
Inclusion Criteria:

- Age is greater than or equal to 18 years.

- Histologically or cytologically confirmed non-CNS primary solid malignancy.

- Pathologically or radiographically confirmed metastatic disease in the brain.
Subjects with non-measurable lesions, including leptomeningeal carcinomatosis, are

- WBRT is clinically indicated, with the exception of prophylactic treatment.

- Karnofsky Performance Status (KPS) greater than or equal to a score of 70.

- Adequate hematology, renal and hepatic function.

- Both men and women of childbearing potential must agree to use adequate contraception
(one of the following listed below) prior to study entry, for the duration of study
participation and up to 2 months following completion of protocol therapy.

- Total abstinence from sexual intercourse (minimum one complete menstrual cycle)

- A vasectomized partner * Hormonal contraceptives (oral, parenteral or
transdermal) for at least 3 months prior to study drug administration

- Double-barrier method (condoms, contraceptive sponge, diaphragm or vaginal ring
with spermicidal jellies or cream)

- Subject is capable of understanding and complying with parameters as outlined in the

- Subject or the subject's legally acceptable representative has voluntarily signed and
dated the informed consent, approved by an Independent Ethics Committee
(IEC)/Institutional Review Board (IRB), prior to the initiation of any screening or
study-specific procedures.

Exclusion Criteria:

- Brain metastases secondary to germ cell tumor or lymphoma malignancy.

- Primary central nervous system (CNS) neoplasm.

- Prior or concurrent administration of the following therapies or treatments:

- Prior treatment with WBRT

- SRS performed less than 14 days prior to WBRT D1, or is scheduled to occur
within 30 days of the last WBRT session

- Last dose of chemotherapy, immunotherapy, biologic therapy, or investigational
therapy was less than 14 days prior to WBRT D1. Bisphosphonates, hormone
modification therapy, and trastuzumab are permitted without restriction

- Unresolved or unstable, serious toxicity from prior administration of another
investigational drug and/or prior anti-cancer treatment.

- Known seizure disorder (status epileptics) that is uncontrolled, or seizures
occurring greater than or equal to 3 times a week over the past month.

- If female, subject is pregnant or breast-feeding.

- Clinically significant and uncontrolled major cardiac, respiratory, renal, hepatic,
gastrointestinal, hematologic or neurological/psychiatric disease or disorder,
including but not limited to:

- Active uncontrolled infection

- Symptomatic congestive heart failure, unstable angina pectoris, or cardiac

- Any other illness condition(s) that could exacerbate potential toxicities,
confound safety assessments, require excluded therapy for management, or limit
compliance with study requirements

- Unable to swallow and retain oral medications.

- Known contraindication to enhanced MRI and CT, including but not limited to:

- Presence of metal objects within the body such as a cardiac pacemaker, implanted
cardiac defibrillator, brain aneurysm clips, cochlear implant, ocular foreign
body, or shrapnel

- History of immediate or delayed hypersensitivity reaction or other
contraindication to contrast agents including but not limited to gadolinium and

- Previous enrollment in this study or another study involving the investigation of
ABT-888, with the exception of receiving a single dose of study drug.

- Consideration by the investigator, for any reason, that the subject is an unsuitable
candidate to receive ABT-888 and/or WBRT.
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