Ropidoxuridine (IPdR)
Oncology drug candidateAn orally administered radiation-sensitizing drug candidate given alongside radiotherapy, currently in a Phase 2 clinical trial in newly diagnosed IDH-wildtype glioblastoma with an unmethylated MGMT promoter.
- Oral radiation sensitizer used in combination with radiotherapy
- FDA 'safe to proceed' letter received January 2024 for the Phase 2 study
- FDA Orphan Drug Designation for glioblastoma
- Phase 2 randomizes patients across 1,200 mg/day and 960 mg/day dose levels