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Glioblastoma Multiforme clinical trials

View clinical trials related to Glioblastoma Multiforme.

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NCT ID: NCT03332355 Terminated - Clinical trials for Glioblastoma Multiforme

Procaspase Activating Compound-1 (PAC-1) in the Treatment of Advanced Malignancies - Component 2

Start date: October 1, 2017
Phase: Phase 1
Study type: Interventional

The primary objectives of this study are to determine the maximal tolerated dose (MTD) of PAC-1 in combination with temozolomide in patients with high grade glioma: glioblastoma multiforme (GBM) or anaplastic astrocytoma after progression following standard first line therapy (Component 2), by evaluation of toxicity and tolerability.

NCT ID: NCT03311542 No longer available - Clinical trials for Glioblastoma Multiforme

Expanded Access for Pembrolizumab (MK-3475)

Start date: n/a
Phase: N/A
Study type: Expanded Access

This is an expanded access program (EAP) for patient with Melanoma and Glioblastoma who have progressed after prior Protocol therapy including Bevacizumab, Temozolomide ( TMZ ), Ipilimumab, BRAF and MEK inhibitors. The patients whose tumors are EGFR, MET or ALK positive should first receive an EFGR or ALK inhibitor, respectively, prior to treatment with pembrolizumab.

NCT ID: NCT03310372 Completed - Clinical trials for Glioblastoma Multiforme

Concomitant Association of Ultrafractionated Brain Irradiation - Temozolomide in Inoperable Primary Glioblastoma Multiforme

TEMOFRAC
Start date: February 13, 2008
Phase: Phase 2
Study type: Interventional

The main purpose of this study is the evaluation of concomitant association of ultrafractionated irradiation and Temodal® in patients with inoperable primary glioblastoma multiforme; study of tolerance and objective response rate. The secondary purposes of this study are the evaluation of progression free survival, global survival and tolerance through toxicity study. The therapeutic response according to methylation or not of MGMT is also evaluated.

NCT ID: NCT03291990 Completed - Clinical trials for Glioblastoma Multiforme

5 Fraction Stereotactic Radiosurgery With Temozolomide for Glioblastoma Multiforme

Start date: October 18, 2017
Phase: Early Phase 1
Study type: Interventional

This investigation is not only to develop an improved radiation/temozolomide approach, but also develop a regimen with potential to form the basis of better combined therapy with immune based treatments.

NCT ID: NCT03276286 Completed - Clinical trials for Glioblastoma Multiforme

Nativis Voyager for Newly Diagnosed GBM

NAT109
Start date: November 10, 2017
Phase: N/A
Study type: Interventional

This feasibility study will assess the effects of the Nativis Voyager therapy in patients newly diagnosed with GBM. The study will enroll and treat up to 32 subjects and will be combined with standard of care radiotherapy and temozolomide.

NCT ID: NCT03235934 Withdrawn - Clinical trials for Glioblastoma Multiforme

Glycemic Impact on Glioblastoma Outcomes

Start date: December 1, 2018
Phase:
Study type: Observational

This pilot study aims to evaluate the feasibility of close glucose monitoring and management of patients (targeting fasting and pre-meal glucose of 4-7 mmol/L) using state-of-the-art flash glucose monitoring (FGM) technology. The glycemic intervention will be personalized based on individual blood glucose levels. Although the glycemic interventions used in this study include standard medications and methods of glucose monitoring used for patients with diabetes, this pilot study will specifically evaluate the feasibility of using these approaches in patients with GBM, appreciating their additional medical, functional and social challenges.

NCT ID: NCT03225963 Recruiting - Clinical trials for Glioblastoma Multiforme

Application of Proteome Profiler Antibody Arrays to Find Angiogenetic Predictors in Glioma Paitents.

Start date: August 1, 2015
Phase: N/A
Study type: Observational

Bevacizumab has become the standard of care of recurrent glioblastoma based on promising clinical trial results with with response rates up to 50% and progression-free survival up to 9 months. In our study, we set to find the serum angiogenesis biomarkers of bevacizumab response.

NCT ID: NCT03225300 Recruiting - Clinical trials for Glioblastoma Multiforme

Simultaneous Integrated Boost in Malignant Glioma Patients Treated With Chemoradiation

Start date: January 1, 2005
Phase: N/A
Study type: Interventional

Simultaneous integrated boost (SIB), a field-in-field escalation technique, has been introduced to deliver higher radiation dose to the certain part of target with the same fractionation scheme. The aim of this study was to investigate the value of chemoradiation (CCRT) using SIB in glioblastoma and the correlation with surgical extent.

NCT ID: NCT03212235 Recruiting - Clinical trials for Glioblastoma Multiforme

Hypofractionated Radiation Therapy for Glioblastoma

Start date: June 5, 2017
Phase: Phase 2
Study type: Interventional

Notwithstanding major improvements in treatment modalities, the prognosis of patients with glioblastoma is poor. Hypofractionated radiation therapy as an alternative of the standard 6-week regimen could be an attractive approach as an effort to prevent tumor cell repopulation and reduction the total treatment period promoting patient comfort and convenience.

NCT ID: NCT03175224 Recruiting - Lung Cancer Clinical Trials

APL-101 Study of Subjects With NSCLC With c-Met EXON 14 Skip Mutations and c-Met Dysregulation Advanced Solid Tumors

SPARTA
Start date: September 27, 2017
Phase: Phase 2
Study type: Interventional

To assess: - efficacy of APL-101 as monotherapy for the treatment of NSCLC harboring MET Exon 14 skipping mutations, NSCLC harboring MET amplification, solid tumors harboring MET amplification, solid tumors harboring MET fusion, primary CNS tumors harboring MET alterations, solid tumors harboring wild-type MET with overexpression of HGF and MET - efficacy of APL-101 as an add-on therapy to EGFR inhibitor for the treatment of NSCLC harboring EGFR activating mutations and developed acquired resistance with MET amplification and disease progression after documented CR or PR with 1st line EGFR inhibitors (EGFR-I)