Enzastaurin to Treat Recurrent Brain Tumor
NCT00108056 · Status: TERMINATED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 26
Last updated 2019-12-05
Summary
This study will examine the safety of a twice-a-day dosing regimen of the experimental drug Enzastaurin in patients with malignant glioma (a cancerous brain tumor) who are and who are not taking certain anti-seizure medicines. Enzastaurin may prevent the formation of new blood vessels that tumors need to grow. It has shown some effect against brain tumors in animals and in some patients with recurrent gliomas. This study will see if the drug can help patients with gliomas and how much drug they should be given.
Patients 18 years of age and older with malignant glioma that has recurred after standard therapy may be eligible for this study. Candidates are screened with a physical examination, blood and urine tests, magnetic resonance imaging (MRI) or computed tomography (CT) scans, and an electrocardiogram.
Participants are divided into two groups of patients-those who are and those who are not taking certain anti-seizure medications-in order to determine if the anti-seizure medication alters the way the body handles Enzastaurin. Patients in both groups are further divided into different dosing regimens: some in each group take Enzastaurin once a day for 3 weeks, followed by twice a day for 3 weeks; others in the group take the drug twice a day for 3 weeks followed by once a day for 3 weeks. The medication is taken by mouth every day. Treatment is given in 6-week cycles and may continue for 1 year unless the tumor grows or the patient develops unacceptable drug side effects. In addition to drug treatment, patients have the following tests and procedures:
* Medical history, physical, and neurological examinations every 3 weeks during the first cycle and then every 6 weeks.
* MRI or CT scan of the head before starting each new cycle. MRI uses a magnetic field and radio waves to produce images of body tissues and organs. CT uses x-rays to provide 3-dimensional views of the part of the body being studied. For both procedures, the patient lies on a table that slides into the cylindrical scanner.
* Routine blood tests every week during the first cycle and every 3 weeks after that.
* Electrocardiogram on days 21 and 42 of the first cycle, just before taking the drug and 30 minutes and 4 hours after taking the drug.
* Pharmacokinetic studies within 3 days of day 21 of the first cycle. Several blood samples are drawn to measure levels of Enzastaurin. Patients taking the drug once a day have blood samples drawn before the morning dose and 1, 2, 4, 6 and 24 hours after the dose. Patients taking the drug twice a day have samples drawn before the morning dose, at 1, 2, 4, 6 and 12 hours after the dose, and then 12 hours after the evening dose. In addition, on day 1 an extra tube of blood is drawn at the time of the Enzastaurin dose and 4 hours later.
* Dynamic MRI with spectroscopy or PET. These tests are done to help distinguish live tumor from dying tumor. The experience of dynamic MRI with spectroscopy is the same as standard MRI and is done at the same time as the standard procedure. PET uses a radioactive substance to show cellular activity in specific tissues of the body. The patient is given an injection of a sugar solution in which a radioactive isotope has been attached to the sugar molecule. A special camera detects the radiation emitted by the radioisotope, and the resulting images show how much glucose is being used in various parts of the body. Because rapidly growing cells, such as tumors, take up and use more glucose than normal cells do, this test can be used to show active tumors.
Conditions
Interventions
- DRUG
-
Enzastaurin (LY317615) monohydronchloride
Sponsors & Collaborators
-
National Cancer Institute (NCI)
lead NIH
Principal Investigators
-
Teri N Kreisl, M.D. · National Cancer Institute (NCI)
Study Design
- Purpose
- TREATMENT
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2005-04-07
- Primary Completion
- 2014-04-01
- Completion
- 2014-04-01
Countries
- United States
Study Locations
More Related Trials
-
Enzastaurin Before and Concomitant With Radiation, Followed by Enzastaurin in Participants With Newly Diagnosed Glioblastoma
NCT00509821 ·Status: COMPLETED ·Phase: PHASE2
-
Study of Enzastaurin Versus Placebo in the Treatment of Patients With Brain Metastases of Lung Cancer, After Whole Brain Radiation Therapy
NCT00415363 ·Status: COMPLETED ·Phase: PHASE2
-
EMD 121974 in Treating Patients With Progressive or Recurrent Glioma
NCT00006093 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
A Study in Recurrent Glioblastoma (GB)
NCT01582269 ·Status: COMPLETED ·Phase: PHASE2
-
Cilengitide in Treating Younger Patients With Recurrent or Progressive High-Grade Glioma That Has Not Responded to Standard Therapy
NCT00679354 ·Status: COMPLETED ·Phase: PHASE2
-
Genetically Modified Stem Cells and Irinotecan Hydrochloride in Treating Patients With Recurrent High-Grade Gliomas
NCT02055196 ·Status: WITHDRAWN ·Phase: PHASE1
-
Carboxylesterase-Expressing Allogeneic Neural Stem Cells and Irinotecan Hydrochloride in Treating Patients With Recurrent High-Grade Gliomas
NCT02192359 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE1
-
Pyrazoloacridine Plus Carboplatin in Treating Patients With Recurrent Glioma
NCT00005976 ·Status: COMPLETED ·Phase: PHASE2
-
Irinotecan in Treating Patients With Recurrent Glioma
NCT00003134 ·Status: COMPLETED ·Phase: PHASE2
-
Irinotecan Plus Carmustine in Treating Patients With Recurrent Primary Malignant Glioma
NCT00002988 ·Status: COMPLETED ·Phase: PHASE1
-
A Trial of Enzastaurin Plus Temozolomide During and Following Radiation Therapy in Patients With Newly Diagnosed Glioblastoma With or Without the Novel Genomic Biomarker, DGM1
NCT03776071 ·Status: COMPLETED ·Phase: PHASE3
-
Bortezomib in Treating Patients With Recurrent Glioma
NCT00006773 ·Status: TERMINATED ·Phase: PHASE1
-
A Dose-Escalation Study in Participants With Recurrent Malignant Glioma
NCT01682187 ·Status: COMPLETED ·Phase: PHASE1
-
Vorinostat and Bortezomib in Treating Patients With Progressive, Recurrent Glioblastoma Multiforme
NCT00641706 ·Status: COMPLETED ·Phase: PHASE2
-
Sorafenib in Treating Patients With Recurrent or Progressive Malignant Glioma
NCT00093613 ·Status: COMPLETED ·Phase: PHASE1
-
Antineoplaston Therapy in Treating Children With Recurrent or Refractory High-Grade Glioma
NCT00003535 ·Status: TERMINATED ·Phase: PHASE2
-
Carmustine in Treating Patients With Progressive or Recurrent Glioblastoma Multiforme
NCT00006656 ·Status: UNKNOWN ·Phase: PHASE2
-
Irinotecan in Treating Patients With Progressive or Recurrent Malignant Glioma
NCT00003616 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Erlotinib in Treating Patients With Recurrent or Progressive Glioblastoma Multiforme
NCT00054496 ·Status: UNKNOWN ·Phase: PHASE2
-
A Study of MEDI-575 in Subjects With Recurrent Glioblastoma Multiforme
NCT01268566 ·Status: COMPLETED ·Phase: PHASE2
-
A Study of Gliadel Followed by Avastin + Irinotecan for Glioblastoma Multiforme (GBM)
NCT00735436 ·Status: TERMINATED ·Phase: PHASE2
-
Study of Recombinant Human Endostatin Combined With CV Regimen in the Treatment of Pediatric Low-grade Gliomas
NCT04659421 ·Status: COMPLETED ·Phase: PHASE2
-
ZD6474 to Treat Advanced Brain Cancer in Patients
NCT00272350 ·Status: COMPLETED ·Phase: PHASE1
-
Tipifarnib in Treating Young Patients With Recurrent or Progressive High-Grade Glioma, Medulloblastoma, Primitive Neuroectodermal Tumor, or Brain Stem Glioma
NCT00070525 ·Status: COMPLETED ·Phase: PHASE2
-
Atrasentan in Treating Patients With Progressive or Recurrent Malignant Glioma
NCT00017264 ·Status: COMPLETED ·Phase: PHASE1