This is a multicenter phase 1 trial of INCB7839 for children with recurrent or progressive high-grade gliomas, including, but not limited to, diffuse intrinsic pontine glioma (DIPG) and other diffuse midline gliomas (DMGs), after upfront therapy.
Age range
3 Years – 21 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Number of Patients Who Experienced Dose-limiting Toxicities (DLTs)
Timeframe: Approximately 28 days
Maximum Tolerated Dose (MTD) and/or Recommend Phase II Dose (RP2D) of INCB7839
Timeframe: Approximately 28 days
Area Under the Curve (AUC) of INCB7839
Timeframe: Up to 3 days after the start of treatment
Maximum Concentration [Cmax] of INCB7839
Timeframe: Up to 3 days after the start of treatment
Apparent Oral Clearance [CL/F] of INCB7839
Timeframe: Up to 3 days after the start of treatment
Time to Reach Maximum Concentration [Tmax] of INCB7839
Timeframe: Up to 3 days after the start of treatment