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Glioma clinical trials

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NCT ID: NCT01991977 Active, not recruiting - Malignant Glioma Clinical Trials

18F-DOPA-PET in Finding Tumors in Patients With Newly Diagnosed Gliomas Undergoing Radiation Therapy

Start date: December 2013
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well fluorine F 18 fluorodopa (18F-DOPA)-positron emission tomography (PET) works in finding tumors in patients with newly diagnosed gliomas undergoing radiation therapy. Comparing results of diagnostic procedures done before and during radiation therapy may help doctors predict a patient's response to treatment and help plan the best treatment.

NCT ID: NCT01952769 Active, not recruiting - DIPG Clinical Trials

Anti PD1 Antibody in Diffuse Intrinsic Pontine Glioma

Start date: February 2014
Phase: Phase 1/Phase 2
Study type: Interventional

Diffuse pontine gliomas are incurable with currently used treatments. based on data stating that progressive tumors inhibit immune system, would try to enhance immune system activity and tumor cell killing. anti PD1 prevents one of the important mechanisms allowing the tumor to supress the immune system thus we hope it will allow for prolonged control of the tumors

NCT ID: NCT01817751 Active, not recruiting - Glioblastoma Clinical Trials

Sorafenib, Valproic Acid, and Sildenafil in Treating Patients With Recurrent High-Grade Glioma

Start date: April 11, 2013
Phase: Phase 2
Study type: Interventional

The purpose of this research study is to test the safety, tolerability, and effectiveness of the combination of three drugs, sorafenib (Nexavar®), valproic acid (Depakote®), and sildenafil (Viagra®), when used to treat high-grade glioma, a type of brain tumor.

NCT ID: NCT01748149 Active, not recruiting - Clinical trials for Pediatric Recurrent/Refractory BRAFV600E-mutant Gliomas

Vemurafenib in Children With Recurrent/Refractory BRAF Gene V600E (BRAFV600E)-Mutant Gliomas

Start date: April 29, 2014
Phase: Early Phase 1
Study type: Interventional

This is a multicenter, safety and pharmacokinetic trial to determine the MTD and/or select a recommended phase 2 dose (RP2D) of vemurafenib in children with recurrent or refractory gliomas containing the BRAFV600E or BRAF Ins T mutation.

NCT ID: NCT01743950 Active, not recruiting - Glioma Clinical Trials

A Phase II Study of Pulse Reduced Dose Rate Radiation Therapy With Bevacizumab

Start date: December 3, 2012
Phase: Phase 2
Study type: Interventional

To determine the efficacy of Pulse Reduced Dose Rate (PRDR) radiation when given in 27 fraction over 5.5 weeks with concurrent bevacizumab followed by adjuvant bevacizumab until time of progression in patients with recurrent high grade gliomas (grade III and grade IV). Patients will be placed in 1 of 4 groups based on their histologic diagnosis and prior exposure to bevacizumab.

NCT ID: NCT01734512 Active, not recruiting - Clinical trials for Pediatric Recurrent Progressive Low-grade Gliomas

PNOC 001: Phase II Study of Everolimus for Recurrent or Progressive Low-grade Gliomas in Children

Start date: December 13, 2012
Phase: Phase 2
Study type: Interventional

This is an open label study of everolimus in children with recurrent or progressive low-grade glioma.

NCT ID: NCT01682187 Active, not recruiting - Glioma Clinical Trials

A Dose-Escalation Study in Participants With Recurrent Malignant Glioma

Start date: December 15, 2005
Phase: Phase 1
Study type: Interventional

This is a study of oral LY2157299 as monotherapy and in combination with lomustine in participants with recurrent malignant glioma.

NCT ID: NCT01672463 Active, not recruiting - Clinical trials for Recurrent Malignant Glioma

Clinical Trial of IV OKN-007 in a Pilot Cohort of Human Recurrent Malignant Glioma Patients

OKN-007
Start date: December 2012
Phase: Phase 1
Study type: Interventional

This is an open label Phase 1b clinical trial of IV administration of OKN-007 in a pilot cohort of human recurrent malignant glioma patients. All patients will have been previously treated with the standard-of-care treatment which includes surgical resection, radiation and chemotherapy, and in some cases treatment for recurrent disease with investigational agents or bevacizumab (Avastin). Patients with unequivocal recurrence (first or greater) established by MRI with and without contrast (e.g., Gd-DTPA (Gadolinium-diethylene triamine pentacetic acid) and meeting inclusion and exclusion criteria, will be eligible for OKN-007 treatment on this protocol.

NCT ID: NCT01638533 Active, not recruiting - Lymphoma Clinical Trials

Romidepsin in Treating Patients With Lymphoma, Chronic Lymphocytic Leukemia, or Solid Tumors With Liver Dysfunction

Start date: June 12, 2012
Phase: Phase 1
Study type: Interventional

This phase I trial studies the side effects and best dose of romidepsin in treating patients with lymphoma, chronic lymphocytic leukemia, or solid tumors with liver dysfunction. Romidepsin may stop the growth of cancer cells by entering the cancer cells and by blocking the activity of proteins that are important for the cancer's growth and survival.

NCT ID: NCT01534845 Active, not recruiting - Clinical trials for Anaplastic Glioma of Brain

Efficacy Study of Radiotherapy Alone Versus CCRT With Temozolomide in Grade III Gliomas Without 1p/19q Codeletion

Start date: March 2012
Phase: Phase 2
Study type: Interventional

1. The management of anaplastic gliomas of WHO grade 3 is currently largely based on surgery followed by radiotherapy, of which prognosis remains still dismal with the median survival of 2-5 years. To date, the benefit of chemo for WHO grade 3 gliomas is unclear of modest at best with conventional cytotoxic agents, and the role of temozolomide for these entities still is not elucidated. 2. Codeletion of chromosome 1p/19q is considered the most important marker of prognostic significance in WHO grade 3 gliomas. 3. To project a randomized phase 2 screening trial examining the efficacy of concurrent chemoradiotherapy with temozolomide followed by adjuvant temozolomide for WHO grade 3 gliomas without codeletion of chromosome 1p/19q. 4. The prognostic significance of methylation status of MGMT and IDH1 mutation as molecular markers will be also assessed in each arm as key secondary analysis.