RecruitingPhase 1NCT06666712

Chronic CED of TPT for Recurrent Malignant Glioma

Chronic Convection Enhanced Delivery of Topotecan for Recurrent Malignant Glioma


Sponsor

Jeffrey N. Bruce

Enrollment

6 participants

Start Date

May 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The primary goal of this study is to establish the safety of chronic Convection Enhanced Delivery (CED) of the chemotherapeutic drug Topotecan for patients with recurrent malignant glioma that harbors the Isocitrate Dehydrogenase mutation (IDH-mut). The secondary goal of the study is to study drug distribution and assess the tumor response to prolonged continuous CED of Topotecan. Convection Enhanced Delivery is a novel method of drug delivery that allows administration of a drug directly to the brain. In CED, a drug pump is placed under the skin in the chest or abdominal region. The pump is connected to a catheter that is tunneled underneath the skin to the brain. The tip of the catheter then infuses Topotecan directly onto the brain tumor. There will be a total of four treatment infusions over the course of 23-29 days, with a 5-7-day rest period between each infusion. Throughout this period, patients' health will be monitored through imaging, blood draws, and regular exams. At the end of the treatment period, the pump will be removed, followed by resection of the tumor. Patients will be followed for the duration of their lives. This is the investigator's second clinical trial studying CED of TPT in recurrent glioma. In the prior Phase 1b trial, chronic pulsatile CED safely and effectively delivered Topotecan to patients with IDH mutant recurrent Glioblastoma (WHO grade 4).


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a way to deliver chemotherapy (topotecan) directly into a brain tumor using a slow-release device implanted during surgery, rather than through the bloodstream. It is for people whose aggressive brain cancer (malignant glioma) has come back after standard treatments have stopped working. **You may be eligible if...** - You are 18 or older - You have a recurrent high-grade brain tumor (WHO grade 3–4) that has a specific genetic mutation (IDH-mutant) and has progressed on imaging - Your tumor is smaller than 32 cc and accessible for surgery - You are in reasonably good health (Karnofsky score ≥ 70) and able to undergo surgery - Your blood counts and organ function are within acceptable ranges **You may NOT be eligible if...** - Your tumor has spread throughout the brain fluid system or affects both brain hemispheres or the cerebellum - You have an active infection or untreated fever - You are HIV-positive or have active hepatitis B or C - You have previously received topotecan for this tumor - You cannot have MRI or PET scans 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

DRUGTopotecan

Topotecan (TPT) is a chemotherapeutic agent that is a topoisomerase inhibitor. This intervention is uniquely distinguished through its administration using an externalized catheter and external microinfusion pump (Convection-Enhanced Delivery)


Locations(1)

Columbia University Irving Medical Center / NewYork-Presbyterian Hospital

New York, New York, United States

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NCT06666712


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