FDA grants Orphan Drug Designation for Cantrixil in AML
“The Orphan Drug Designation is an important regulatory milestone for the development of Cantrixil. It gives us development incentives in the U.S. and the possibility of seven years of market exclusivity upon approval. Together with the positive preclinical results generated to date, the designation strengthens the foundation for advancing Cantrixil toward a Phase I study in AML” says Erik Kinnman, CEO of Vivesto.
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