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Study details
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Lorlatinib for Newly-Diagnosed High-Grade Glioma With ROS or ALK Fusion

Nationwide Children's Hospital
NCT IDNCT06333899ClinicalTrials.gov data as of Apr 2026
Phase

EARLY_PHASE1

Ages

1–21

Locations

10 sites in CO, DC, IL +6

What this study is about

This EARLY_Phase 1 study is testing Lorlatinib in people with anaplastic astrocytoma. The primary outcome being measured is Disease Control Rate.

Simplified from trial records by PatientMatch.

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Oral

How treatment is administered

Treatment Assignment
Standard assignment

Assignment is predetermined by the study protocol.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

lorlatinib, ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS

Drug routes

oral

Endpoints

Primary: Disease Control Rate, Number of participants with lorlatinib-related adverse events as assessed by CTCAE v5.0

Secondary: Associations between genomic tumor alterations with radiographic response, Objective Response Rate (ORR) in HGG, Overall Survival (OS) in HGG, Progression-Free Survival in HGG

Body systems

Oncology