29 Participants NeededMy employer runs this trial

Novel Therapies for Brain Cancer

PO
Overseen ByPNOC Operations Office
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests new treatments for individuals with recurrent or progressive atypical teratoid rhabdoid tumors (ATRT), a type of brain cancer. The study aims to evaluate the safety and effectiveness of a combination of two drugs: gemcitabine (a chemotherapy drug) and paxalisib (a potential new treatment). Participants will receive these drugs over a series of cycles to determine the optimal dosage and assess their impact on the tumor. The trial seeks individuals diagnosed with ATRT that has returned or worsened after previous treatments. As a Phase 2 trial, this research focuses on measuring the treatment's effectiveness in an initial, smaller group of people.

Do I have to stop taking my current medications for the trial?

The trial requires a washout period (time without taking certain medications) for previous cancer treatments before you can join. If you're on corticosteroids, you need to be on a stable or decreasing dose for at least a week before enrolling. The protocol doesn't specify about other medications, so it's best to discuss with the trial team.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

A previous study showed that combining gemcitabine and paxalisib could slow tumor growth and significantly extend survival time, with average survival increasing from 22 days to 82.5 days. This suggests it could effectively treat certain brain cancers.

Research on paxalisib alone has shown it to be generally safe. It has been studied in various cancer types and has received special recognition from the FDA for treating glioblastoma, a type of brain cancer, indicating its promise for rare conditions.

Gemcitabine is a well-known chemotherapy drug often used in cancer treatment. Its successful use in other cancers suggests it might be safe for brain cancer when combined with paxalisib.

Overall, existing research supports the safety of both gemcitabine and paxalisib, especially when used together. The current trial will further assess how well participants tolerate this combination.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about the combination of gemcitabine and paxalisib for treating brain cancer because it targets the disease in a novel way. Unlike traditional treatments like surgery, radiation, and temozolomide, which primarily focus on removing or shrinking tumors, paxalisib inhibits a specific pathway called PI3K, which is crucial for cancer cell survival and growth. Combining this with gemcitabine, a chemotherapy drug known for its ability to prevent cancer cells from reproducing, could offer a more powerful one-two punch against the cancer. This innovative approach has the potential to improve outcomes for patients who have few options beyond the standard treatments.

What evidence suggests that this trial's treatments could be effective for brain cancer?

Research has shown that combining gemcitabine and paxalisib may help treat aggressive brain tumors. In lab studies, this combination increased the average survival time from 22 days to 82.5 days. Participants in this trial will receive this combination therapy to evaluate its effectiveness. Paxalisib alone has also extended survival for patients with glioblastoma, a type of brain cancer, by several months. This suggests that paxalisib, especially when combined with gemcitabine, could be effective against certain brain cancers like ATRT (atypical teratoid/rhabdoid tumor). This combination works by slowing tumor growth and may improve patient outcomes.15678

Who Is on the Research Team?

SM

Sabine Mueller, MD, PhD

Principal Investigator

University of California, San Francisco

AM

Ashley Margol, MD, MS

Principal Investigator

Children's Hospital Los Angeles

Are You a Good Fit for This Trial?

This trial is for children, teens, and young adults (ages 1–39) with a specific type of brain cancer called ATRT that has come back or gotten worse. Participants must have certain lab results, be able to swallow capsules, not be pregnant or breastfeeding, and meet other health requirements.

Inclusion Criteria

Participants must meet performance score criteria.
Participants must have confirmation of methylation report, co-enrollment on PNOC-030 or sufficient tumor tissue available for methylation-based subgrouping
Participants must comply with contraception requirements.
See 12 more

Exclusion Criteria

I am not pregnant or breastfeeding.
Participants must not have a history of allergic reactions to compounds of similar composition as the intended treatment regimen.
I do not have any uncontrolled infections or serious illnesses.
See 3 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment Phase I

Participants receive a combination of gemcitabine and paxalisib to determine the recommended Phase 2 dose (RP2D).

4 weeks
3 visits (in-person) for infusion on days 1, 8, and 15

Treatment Phase II

Participants receive a combination of gemcitabine and paxalisib over a 28-day cycle, for up to 24 cycles or until they meet criteria to stop treatment.

up to 2 years
3 visits (in-person) per cycle for infusion on days 1, 8, and 15

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 months

What Are the Treatments Tested in This Trial?

Interventions

  • Gemcitabine
  • Paxalisib

Trial Overview

The study is testing new treatments and combinations—including drugs like Paxalisib and Gemcitabine—on people with recurrent/progressive ATRT. It uses multiple treatment groups to see which therapies are safe and effective.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Group I: Treatment Arm A: Phase IExperimental Treatment6 Interventions
Group II: Treatment Arm A: Efficacy (Phase II)Experimental Treatment6 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

Sabine Mueller, MD, PhD

Lead Sponsor

Trials
9
Recruited
440+

Pacific Pediatric Neuro-Oncology Consortium

Collaborator

Trials
16
Recruited
840+

Rally Foundation

Collaborator

Trials
2
Recruited
8,000+

Citations

ATRT-15. COMBINING THE PI3K INHIBITOR PAXALISIB ...

Paxalisib monotherapy significantly extends median survival in murine models compared to vehicle controls (CHLA-06: 40 to 54 days, p=0.001; BT-12: 21 to 35 days ...

Paxalisib Continues to Provide Survival Benefit Over SOC ...

Paxalisib improved median OS to 15.54 months in newly diagnosed glioblastoma with unmethylated MGMT, compared to 11.89 months with SOC. No ...

Safety, Pharmacokinetics and Efficacy of Paxalisib (GDC ...

This phase 2 study is an open-label, multicenter, dose-escalation and expansion study to assess the safety, tolerability, recommended phase 2 dose (RP2D), ...

Paxalisib Shows Early Efficacy in Newly Diagnosed ...

Paxalisib had a strong signal of clinical efficacy in patients with newly diagnosed glioblastoma, according to the interim analysis of a ...

ATRT-09. COMBINATION OF THE PI3K INHIBITOR ... - PMC

Paxalisib/Gemcitabine combination therapy slows tumor growth (Bioluminescent imaging) and extends median survival from 22 to 82.5 days.

Kazia-Therapeutics-Reports-Encouraging-Preliminary- ...

Paxalisib was granted Orphan Drug Designation for glioblastoma by the U.S. Food and Drug Administration (FDA) in February 2018, and Fast Track ...

FDA Signals Potential for Standard Approval of Paxalisib in ...

The FDA indicated paxalisib's overall survival data could support standard approval in glioblastoma, as supported by GBM-AGILE study findings.

Safety, Pharmacokinetics and Efficacy of Paxalisib (GDC-0084 ...

This phase 2 study is an open-label, multicenter, dose-escalation and expansion study to assess the safety, tolerability, recommended phase 2 ...