RecruitingPhase 1Phase 2NCT06161519

PLX038 in Primary Central Nervous System Tumors Containing MYC or MYCN Amplifications

Phase I/II Trial of PLX038 in Primary Central Nervous System Tumors With and Without MYC or MYCN Amplifications


Sponsor

National Cancer Institute (NCI)

Enrollment

146 participants

Start Date

Jan 31, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Background: About 90,000 new cases of brain and spinal cord tumors are diagnosed annually in the United States. Most of these tumors are benign; however, about 30% are malignant, and 35% of people with malignant tumors in the brain and spinal cord will die within 5 years. Many of these people have changes in certain genes (MYC or MYCN) that drive the development of their cancers. Objective: To test a study drug (PLX038) in people with tumors of the brain or spinal cord. Eligibility: People aged 18 years or older with a tumor of the brain or spinal cord. Some participants must also have tumors with changes in the MYC or MYCN genes. Design: Participants will be screened. They will have a physical exam and blood tests. They will have imaging scans and a test of their heart function. They may need to have a biopsy: A sample of tissue will be removed from their tumor. PLX038 is given through a tube attached to a needle inserted into a vein in the arm. All participants will receive PLX038 on the first day of each 21-day treatment cycle. They will take a second drug 3 days later to help reduce the risk of infection; for this drug, participants will be shown how to inject themselves under the skin at home. Blood tests, imaging scans, and other tests will be repeated during study visits. Hair samples will also be collected during these visits. Some participants may have an additional biopsy. Study treatment will continue up to 7 months. Follow-up visits will continue every few months for up to 5 years.


Eligibility

Min Age: 18 YearsMax Age: 120 Years

Plain Language Summary

Simplified for easier understanding

This study tests PLX038, a new drug, in people with brain tumors (primary CNS tumors) that have a specific genetic change called a MTAP deletion. This genetic change may make tumor cells more vulnerable to this drug. The study looks at safety and how well the drug works. **You may be eligible if...** - You are 18 or older - You have a primary brain or central nervous system tumor with MTAP gene deletion (confirmed by testing) - Your tumor has come back or is not responding to prior treatments - You have adequate organ function (liver, kidneys, blood counts) - Your performance status allows you to be up and about most of the day (ECOG 0–2) **You may NOT be eligible if...** - You cannot have an MRI scan - You have serious active infections or uncontrolled medical conditions - You are on medications that strongly interact with the study drug - You are pregnant or breastfeeding - You received recent chemotherapy or radiation without enough recovery time Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPLX038

PLX038 is given intravenously (IV) at the assigned dose level over about 1 hour on day 1 of each 21-day cycle


Locations(1)

National Institutes of Health Clinical Center

Bethesda, Maryland, United States

View Full Details on ClinicalTrials.gov

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NCT06161519


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