Ropidoxuridine (IPdR)
Oncology drug candidate
An 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
- Enrolling at academic cancer centers including Georgetown, UNC, UVA, Allegheny Health Network and Miami Cancer Institute
Built for
Radiation oncologists and cancer centers treating patients with glioblastoma and other radiation-treated solid tumors, plus drug-discovery researchers for the Molecule.ai platform