Trial of Newly Diagnosed High Grade Glioma Treated With Concurrent Radiation Therapy, Temozolomide and BMX-001
This is a Phase 2 study of newly diagnosed patients with high grade glioma (HGG) undergoing standard radiation therapy and temozolomide treatment. BMX-001 added to radiation therapy and temozolomide has the potential not only to benefit the survival of high grade glioma patients but also to protect against deterioration of cognition and impairment of quality of life. BMX-001 will be given subcutaneously first with a loading dose zero to four days prior to the start of chemoradiation and followed by twice a week doses at one-half of the loading dose for the duration of radiation therapy plus two weeks. Both safety and efficacy of BMX-001 will be evaluated. Impact on cognition will also be assessed. Eighty patients will be randomized to the treatment arm that will receive BMX-001 while undergoing chemoradiation and 80 patients randomized to receive chemoradiation alone. The investigators hypothesize that BMX-001 when added to standard radiation therapy and temozolomide will be safe at pharmacologically relevant doses in patients with newly diagnosed high grade glioma. The investigators also hypothesize that the addition of BMX-001 will positively impact the overall survival and improve objective measures of cognition in newly diagnosed high grade glioma patients.
A Phase 2 Trial for Patients With Newly Diagnosed High Grade Glioma Treated With Concurrent Radiation Therapy, Temozolomide, and BMX-001
160 patients will be enrolled and randomized with a treatment arm allocation ratio of 1:1 in this Phase 2 study. At enrollment, patients will be assessed with patient history, physical/neurological examinations, standard laboratory evaluations (CBC with differential and comprehensive metabolic panel (CMP)), baseline MRI brain with and without gadolinium, cognitive testing and patient-reported outcome questionnaires of HRQoL. On the first day of BMX-001 (loading dose), patients will be evaluated with patient history, patient physical/neurological examinations, and standard laboratory evaluations (CBC with differential and CMP). Patients in Arm A will be administered BMX-001 subcutaneously first as a loading dose on the day before the start of chemo¬radiation and then at maintenance dose (50% of the loading dose) twice a week for 8 weeks. Because oxidative stress continues to occur for up to several weeks following RT, the proposed protocol includes administering BMX-001 both before the start of RT and continuing for 2 weeks after the comple¬tion of RT and TMZ. TMZ will be dosed at 75 mg/m2 orally daily for 42 days and RT will be delivered in daily fractions of 1.8-2 Gy given 5 days a week for 6 weeks for a total of 59.4-60 Gy. During standard RT and TMZ, CBC with differential will be obtained weekly and CMP will be obtained every 4 weeks. Two weeks after the completion of standard RT and TMZ and every 8 weeks during adjuvant TMZ, patients will be evaluated with the following: patient history, physical/neurological examinations, Brain MRI with and without gadolinium, cognitive testing and patient-reported outcome questionnaires of HRQoL. Two weeks after the completion of chemoradiation, patients will transition to adjuvant chemotherapy with TMZ dosed at 150-200 mg/m2 orally for 5 days of a 28-day cycle for a total of 12 cycles. In light of the findings that BMX-001 can spare radiation-induced hair loss in a mouse model , we will evaluate and describe hair loss as an exploratory outcome in HGG patients by evaluating hair at baseline and then every 8 weeks. Another exploratory endpoint, based on pre¬clinical findings that BMX-001 protects white matter from radiation-induced damage , will be white matter integrity assessed using MRI diffusion tensor imaging. This will be obtained after enrollment, 2 weeks after the completion of standard RT and TMZ, and 24 weeks after the start of standard RT and TMZ. Patients will be discontinued from the study if they experience progression of disease, death or withdraw informed consent.
High Grade Glioma, GlioblastomaGlioblastomaGliomaTemozolomideManganeseBMX-001Radiation TherapyRadiation Therapy, TMZ and BMX-001Radiation Therapy and TMZ
You can join if…
Open to people ages 18 years and up
- Subjects must have histologically confirmed diagnosis of World Health Organization (WHO) grade III or IV malignant glioma
- Subjects must be planning to start standard of care radiation therapy and chemotherapy
- Subjects must be within 12 weeks of last major neurosurgical procedure for the high-grade glioma (craniotomy, open biopsy, or stereotactic biopsy)
- Subjects must have had a definitive resection with residual radiographic contrast enhancement on post-resection CT or MRI of less than or equal to 2 cm in any two perpendicular planes on any images
- Age * 18 years
- Karnofsky Performance Status (KPS) ≥ 70%
- Hemoglobin ≥ 9.0 g/dl, absolute neutrophil count (ANC) ≥ 1,500 cells/µl, platelets ≥ 125,000 cells/µl
- Serum creatinine ≤ 1.5 mg/dl, serum glutamate oxaloacetate transaminase (SGOT) and bilirubin ≤ 1.5 times upper limit of normal
- Signed informed consent approved by the Institutional Review Board
- If sexually active, patients must agree to use appropriate contraceptive measures for the duration of the study and for 12 months afterwards as stated in the informed consent
- Stable and/or decreasing dose of corticosteroids for greater than or equal to 7 days.
You CAN'T join if...
- Pregnancy or breast-feeding
- Active infection requiring IV antibiotics 7 days before enrollment
- Signs of wound-healing problems or infection at the craniotomy/biopsy site.
- Prior, unrelated malignancy requiring current active treatment with the exception of cervical carcinoma in situ and adequately treated basal cell or squamous cell carcinoma of the skin
- Co-medication that may interfere with study results; e.g. immuno-suppressive agents other than corticosteroids
- Prior treatment with radiotherapy or chemotherapy for a brain tumor, irrespective of the grade of the tumor
- Evidence of > grade 1 CNS hemorrhage on baseline MRI on CT scan
- Systemic treatment with inducers or strong inhibitors of cytochrome P450 within four days before enrollment or planned treatment during the time period of the study.
- Metal in the body (except dental fillings) e.g., pacemaker, infusion pump, metal aneurysm clip, metal prosthesis, joint, rod or plate.
- Severe allergy to contrast agent.
- Univeristy of California San Francisco
not yet accepting patients
San FranciscoCalifornia94143United States
- University of California Los Angeles
not yet accepting patients
Los AngelesCalifornia90095United States
- accepting new patients
- Start Date
- Completion Date
- BioMimetix JV, LLC
- Phase 2
- Study Type
- Last Updated
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