Clinical trial for Glioblastoma
Official title VISTA: Valproic Acid, Irinotecan, and Simvastatin for Recurrent Glioma
ClinicalTrials.gov ID: NCT07831369
What this study is testing
What is Valproic Acid (VPA)?
Valproic Acid (VPA) is an investigational medicine, given as a once-daily IV infusion (through a vein), being studied as a potential treatment for glioblastoma.
Plain-language explanation of the investigational treatment. It is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- The goal of this clinical trial is to see if the combination of valproic acid, irinotecan, and simvastatin causes these tumors to stabilize or shrink, which is a sign that these combinations are effective against tumors in patients with recurrent glioblastoma and adults with recurrent IDH-mutated gliomas
- Phase 2: a mid-size study of how well it works
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 98
You may be able to join if
- Diagnosis of glioblastoma or IDH-mutated glioma by WHO 2021 classification
- For glioblastoma, at least one prior treatment, which needs to include temozolomide and/or radiation
- For IDH-mutated glioma, prior treatment with both radiation and alkylating chemotherapy
- Evidence of progression by RANO 2.0 criteria on MRI within last four weeks
- At least 1 enhancing measurable lesion
You likely can't join if
- Use of an enzyme-inducing antiepileptic or other strong inducer of CYP3A4
- Prior treatment with irinotecan
- Prior use of valproic acid within 2 months
- Anticancer treatment within 4 weeks, 6 weeks if nitrosourea
- Active bacterial or fungal infection requiring systemic treatment
- Pregnancy
See the full eligibility criteria
- Diagnosis of glioblastoma or IDH-mutated glioma by WHO 2021 classification
- For glioblastoma, at least one prior treatment, which needs to include temozolomide and/or radiation
- For IDH-mutated glioma, prior treatment with both radiation and alkylating chemotherapy
- Evidence of progression by RANO 2.0 criteria on MRI within last four weeks
- At least 1 enhancing measurable lesion
- Use of an enzyme-inducing antiepileptic or other strong inducer of CYP3A4
- Prior treatment with irinotecan
- Prior use of valproic acid within 2 months
- Anticancer treatment within 4 weeks, 6 weeks if nitrosourea
- Active bacterial or fungal infection requiring systemic treatment
- Pregnancy
- Known mitochondrial disease
The study team makes the final eligibility decision.
Where it is enrolling
- Fairfax, Virginia, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part, but confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 98 years. The study team makes the final eligibility decision.
Where is this trial taking place?
This study is enrolling now at Fairfax, Virginia, United States. Enter your location above to see the nearest enrolling site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool that is independent of the study sponsor. Details come from ClinicalTrials.gov. The study team decides eligibility, and your own doctor gives medical advice.