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Glioblastoma clinical trials

View clinical trials related to Glioblastoma.

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NCT ID: NCT03603405 Recruiting - Glioblastoma Clinical Trials

HSV-tk and XRT and Chemotherapy for Newly Diagnosed GBM

Start date: February 28, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

Study to assess the safety and efficacy of HSV-tk (gene therapy), valacyclovir, radiotherapy and chemotherapy in newly diagnosed glioblastoma multiforme (GBM) or anaplastic astrocytoma (AA).

NCT ID: NCT03603379 Completed - Glioblastoma Clinical Trials

Doxorubicin-loaded Anti-EGFR-immunoliposomes (C225-ILs-dox) in High-grade Gliomas

GBM-LIPO
Start date: November 16, 2018
Phase: Phase 1
Study type: Interventional

Anti-EGFR-immunoliposomes loaded with doxorubicin (C225-ILs-dox) are given intravenously in patients with relapsed or refractory high-grade gliomas. The pharmacokinetics of C225-ILs-dox in peripheral blood (PB), cerebro-spinal fluid (CSF) and resected tumour tissue will be assessed.

NCT ID: NCT03596086 Recruiting - Clinical trials for Glioblastoma Multiforme

HSV-tk + Valacyclovir + SBRT + Chemotherapy for Recurrent GBM

Start date: December 11, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

Study to assess the safety and efficacy of HSV-tk (gene therapy), valacyclovir, radiotherapy and chemotherapy in recurrent glioblastoma multiforme.

NCT ID: NCT03593993 Terminated - Glioblastoma Clinical Trials

A Biospecimen Collection Study in BRAF-V600E Mutated Recurrent Gliomas

Start date: May 19, 2018
Phase:
Study type: Observational

This is a surgical biospecimen collection study. The purpose of this study is to understand how much of two drugs (dabrafenib and trametinib) are able to penetrate brain tumors and turn off the RAF signaling pathway. This is important because these drugs are currently FDA approved for other tumors and may have efficacy in brain tumors with the BRAF V600E mutation.

NCT ID: NCT03587038 Active, not recruiting - Glioblastoma Clinical Trials

OKN-007 in Combination With Adjuvant Temozolomide Chemoradiotherapy for Newly Diagnosed Glioblastoma

Start date: September 3, 2018
Phase: Phase 1
Study type: Interventional

This is a pilot study exploring the potential benefit of adding OKN-007 with Temozolomide for treatment in patients with malignant Glioblastoma undergoing adjuvant concomitant radiotherapy. This drug combination is expected to have an anti-cancer effect in patients who have experienced disease progression after first line treatment.

NCT ID: NCT03582514 Recruiting - Clinical trials for Glioblastoma Multiforme

PreOperative Brain Irradiation in Glioblastoma

POBIG
Start date: April 19, 2022
Phase: Phase 1
Study type: Interventional

PreOperative Brain Irradiation in Glioblastoma (POBIG) is a phase I study that will test the safety and feasibility of a single fraction of preoperative radiotherapy in patients with a new radiological diagnosis of glioblastoma (GBM). After the single fraction of radiotherapy, patients will receive standard treatment. The standard treatment consists of resection of the tumor followed by (chemo)radiation (i.e. radiotherapy +/- daily temozolomide (75mg/m2) for 6 weeks (60Gy/30fr) or for 3 weeks (40Gy/15fr)).

NCT ID: NCT03581292 Active, not recruiting - Glioblastoma Clinical Trials

Veliparib, Radiation Therapy, and Temozolomide in Treating Patients With Newly Diagnosed Malignant Glioma Without H3 K27M or BRAFV600 Mutations

Start date: November 6, 2018
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well veliparib, radiation therapy, and temozolomide work in treating patients with newly diagnosed malignant glioma without H3 K27M or BRAFV600 mutations. Poly adenosine diphosphate (ADP) ribose polymerases (PARPs) are proteins that help repair DNA mutations. PARP inhibitors, such as veliparib, can keep PARP from working, so tumor cells can't repair themselves, and they may stop growing. Radiation therapy uses high energy x-rays to kill tumor cells and shrink tumors. Drugs used in chemotherapy, such as temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving veliparib, radiation therapy, and temozolomide may work better in treating patients with newly diagnosed malignant glioma without H3 K27M or BRAFV600 mutations compared to radiation therapy and temozolomide alone.

NCT ID: NCT03573986 Terminated - Clinical trials for Recurrent Glioblastoma

Pilot Study of 18F-FMISO PET/CT and MRI Imaging to Explore Tissue Hypoxia and Arteriovenous Shunting in Subjects With Recurrent Glioblastoma Before and After Bevacizumab Treatment

Start date: April 18, 2018
Phase: Phase 1
Study type: Interventional

Subjects with recurrent glioblastoma who are candidates for bevacizumab treatment according to standard of care will be eligible for this study. Positron emission tomography (PET/CT) imaging will use the investigational radiotracer [18F]FMISO to image the brain and evaluate for hypoxia pre and post therapy.. Subjects will also undergo up to three Brain MRIs.

NCT ID: NCT03567135 Recruiting - Glioblastoma Clinical Trials

Temozolomide Plus Anti-angiogenesis Drugs and Radiotherapy as a Treatment for Glioblastoma

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

Temozolomide (TMZ) is an oral chemotherapy drug. It is an alkylating agent used as a first-line treatment for glioblastoma. This methylation damages the DNA and triggers the death of tumor cells. According to the results of several clinical studies, TMZ synchronous plus radiotherapy and subsequent as adjuvant therapy can significantly improve the survival rate of newly diagnosed glioblastoma patients.

NCT ID: NCT03561207 Active, not recruiting - Ovarian Cancer Clinical Trials

3D Prediction of Patient-Specific Response

3D-PREDICT
Start date: June 11, 2018
Phase:
Study type: Observational [Patient Registry]

This is a prospective, non-randomized, observational registry study evaluating a patient-specific ex vivo 3D (EV3D) assay for drug response using a patient's own biopsy or resected tumor tissue for assessing tissue response to therapy in patients with advanced cancers, including ovarian cancer, high-grade gliomas, and high-grade rare tumors.