Shuttle Pharma Finalizes Agreements With All Six Of The Planned Site Enrollment Locations To Administer Phase 2 Clinical Trial Of Ropidoxuridine For Treatment Of Patients With Glioblastoma
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Shuttle Pharma has finalized agreements with six sites for a Phase 2 clinical trial of Ropidoxuridine, a radiation sensitizer for glioblastoma treatment. The drug has received Orphan Drug Designation from the FDA, which could provide marketing exclusivity upon approval.
October 28, 2024 | 8:10 pm
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Shuttle Pharma has secured agreements for a Phase 2 trial of its lead candidate, Ropidoxuridine, for glioblastoma treatment. The drug's FDA Orphan Drug Designation could lead to marketing exclusivity.
The finalization of agreements for the Phase 2 trial is a significant step forward in the development of Ropidoxuridine, potentially increasing investor confidence. The FDA Orphan Drug Designation adds value by offering potential marketing exclusivity, which is a positive indicator for future revenue streams.
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IMPORTANCE 80
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