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Optic Nerve Glioma clinical trials

View clinical trials related to Optic Nerve Glioma.

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NCT ID: NCT02976441 Withdrawn - Astrocytoma Clinical Trials

Autologous Stem Cell Collection and Reinfusion in Newly Diagnosed High Grade Gliomas

Start date: January 2017
Phase: Early Phase 1
Study type: Interventional

The investigators hypothesize that this study will show that sufficient lymphocyte stem cell can be harvested prior chemoradiation and be reinfused back after treatment, and at least 5 of the 10 patients (50%) will achieve an absolute increase of lymphocyte counts of 300 cells/mm^3 four weeks after stem cell reinfusion in high grade glioma patients.

NCT ID: NCT02194452 Withdrawn - Adult Glioblastoma Clinical Trials

Efficacy of 68Ga-DOTATOC Positron Emission Tomography (PET) CT in Children and Young Adults With Brain Tumors

Start date: September 2013
Phase: N/A
Study type: Interventional

This pilot clinical trial studies gallium Ga 68-edotreotide (68Ga-DOTATOC) positron emission tomography (PET)/computed tomography (CT) in finding brain tumors in younger patients. Diagnostic procedures, such as gallium Ga 68-edotreotide PET/CT imaging, may help find and diagnose brain tumors.

NCT ID: NCT01260103 Withdrawn - Optic Nerve Glioma Clinical Trials

Phase 3 Study of ANP Therapy vs. TMZ for Optic Pathway Glioma

Start date: December 2011
Phase: Phase 3
Study type: Interventional

Primary Objectives To compare progression free survival (PFS), the time from randomization to progressive disease,in children with optic pathway glioma (OPG) age ≥ 6 months to < 18 years, who receive combination antineoplaston therapy (ANP therapy) vs. temozolomide (TMZ); study subjects will have 1) received prior treatment with carboplatin or cisplatin, which was terminated secondary to toxicity or progression of OPG, or 2) developed recurrence of OPG after completion of carboplatin or cisplatin therapy. PFS data will be censored on the date of the last tumor assessment documenting absence of progression for study subjects: - Who are alive, on study and are progression-free at the time of the analysis; - Who discontinue, receive no subsequent therapy and are progression-free at the time of the analysis; - Who are given/change therapy other than the study treatment prior to observing progression; - Who discontinued (due to personal preference or toxicity) with a change in therapy, withdrew, or was lost to follow-up; - For whom documentation of disease progression or death occurs after ≥ 2 consecutive missed tumor assessments. - To describe the toxicity profile for ANP therapy vs. TMZ. Secondary Objectives: - To compare overall survival (OS) for subjects treated with ANP therapy vs. TMZ; - To compare disease stabilization rates for subjects treated with ANP therapy vs. TMZ; - To compare complete response (CR), partial response (PR), stable disease (SD), and progressive disease (PD) rates for subjects treated with ANP therapy vs. TMZ.