Clinical Trial Details
Braintumor Website

[Information provided by: ClinicalTrials.gov, which provides patients, family members, and members of the public easy and free access to information on clinical studies for a wide range of diseases and conditions.]

NCT01475006 : AMG 595 First-in-Human in Recurrent Gliomas
PhasePhase 1
AgesMin: 18 Years Max: N/A
Eligibility
Inclusion Criteria:

- Karnofsky performance score > or = 70%

- Must have pathologically documented, and definitively diagnosed recurrent WHO Grade
IV advanced malignant glioblastoma multiforme (Part 1 and Part 2) and/or WHO Grade
III anaplastic astrocytoma (Part 1 only).

- GBM and/or AA tumors expressing EGFRvIII as assessed on archived tissue by IHC
staining of sections containing a minimum of 100 evaluable tumor cells.

- Archived tumor tissue from the initial diagnosis or subsequent relapse(s) of Grade IV
advanced malignant glioblastoma multiforme or Grade III anaplastic astrocytoma
available for submission to central review.

- Subjects with recurrent disease (confirmed by MRI and evaluable by Macdonald
criteria) at the time of first or second recurrence or progression following initial
definitive therapy(s)

- QTcF ? 470 msec

- Hematological function, as follows: Absolute neutrophil count (ANC) ? 1.5 x 10^9/L,
Platelet count ? 100 x 10^9/L, Hemoglobin > 9 g/dL

- Renal function, as follows: Estimated glomerular filtration rate using the Modified
Diet in Renal Disease (MDRD) equation > 45 mL/min/1.73m^2, Urinary protein
quantitative value of < 30 mg/dL in urinalysis or ? 1+ on dipstick, unless
quantitative protein is < 500 mg in a 24 hr urine sample

Exclusion Criteria:

- History of central nervous system bleeding as defined by stroke or intraocular bleed
(including embolic stroke) within 6 months before enrollment.

- Evidence of acute intracranial / intratumoral hemorrhage, except for subjects with
stable grade 1 hemorrhage.

- Peripheral sensory neuropathy > Grade 2.

- Clinically significant ECG changes which obscure the ability to assess the PR, QT,
and QRS interval; congenital long QT syndrome.

- Recent infection requiring intravenous anti-infective treatment that was completed ?
14 days before enrollment.

- Received radiation therapy within 12 weeks before enrollment or has not recovered
from the toxic effects of such therapy.

- For Part 1 (dose escalation): Treatment with bevacizumab or antiangiogenic therapy
within 4 weeks before enrollment, or for Part 2 (dose expansion): any prior
treatment with bevacizumab or antiangiogenic therapy.
LinksPermanent Link to THIS page: https://virtualtrials.com/nct/display1trial.cfm?nct=NCT01475006      |      Link to official Clinicaltrials.gov listing
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