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

NCT01817751 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 47

Last updated 2024-07-17

Study results available
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Summary

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.

Conditions

  • Glioblastoma
  • Recurrent Adult Brain Neoplasm
  • Malignant Glioma
  • WHO Grade III Glioma

Interventions

DRUG

sorafenib tosylate

Given by mouth

DRUG

valproic acid

Given by mouth

DRUG

sildenafil citrate

Given by mouth

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH
  • Virginia Commonwealth University

    lead OTHER

Principal Investigators

  • Andrew Poklepovic, MD · Massey Cancer Center

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-04-11
Primary Completion
2020-08-27
Completion
2023-05-12
FDA Drug
Yes

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01817751 on ClinicalTrials.gov