Stopped: Withdrawal of support from BMS
This research study is evaluating the safety, tolerability and preliminary efficacy of the drugs marizomib and panobinostat in pediatric patients with diffuse intrinsic pontine glioma (DIPG). The names of the study drugs involved in this study are: * Marizomib * Panobinostat
Age range
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.
Dose-limiting toxicity (DLT) of marizomib as a single agent
Timeframe: 28 Days
Dose-limiting toxicity (DLT) of marizomib in combination with panobinostat
Timeframe: 28 days
Maximum Tolerated Dose of Marizomib (single agent)
Timeframe: 28 Days
Maximum Tolerated Dose of Marizomib in combination with panobinostat
Timeframe: 28 Days
Pharmacokinetic parameters-volume of the central compartment (Vc/F)
Timeframe: Day 1 Course A1
Pharmacokinetic parameters-elimination rate constant (Ke),
Timeframe: Course A1, Day 1
Pharmacokinetic parameters half-life (t1/2)
Timeframe: Course A1, Day 1
Pharmacokinetic parameters-apparent clearance (CL/F)
Timeframe: Course A1, Day 1
Area under the plasma concentration time curve (AUC)
Timeframe: Course A1, Day 1