Condition: Central Nervous System Neoplasms · Glioblastoma · Gliosarcoma, Adult · Sponsor: Jazz Pharmaceuticals
The primary objective of this Phase 1, open-label, dose-escalation, and exploratory study is to evaluate the safety and tolerability profile (establish the maximum-tolerated dose) and evaluate the occurrence of dose-limiting toxicities (DLTs) following single weekly or multiple-day weekly dose regimens of single-agent, oral ONC206 in patients with recurrent, primary central nervous system (CNS) neoplasms.
This description comes directly from the study's public registry record.
Clinical Trial Disclosure & Transparency · 215-832-3750 · ClinicalTrialDisclosure@jazzpharma.com
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| National Institutes of Health | Bethesda, Maryland, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT04541082