The Orphan Drug Designation underscores the significant unmet medical need and will grant LR 09 seven-year marketing exclusivity following drug approval by the FDA Zug, Switzerland, 28 February 2023: Laevoroc...
The Orphan Drug Designation underscores the significant unmet medical need and will grant LR 09 seven-year marketing exclusivity following drug approval by the FDA Zug, Switzerland, 28 February 2023: Laevoroc...
UCLA data in the Journal of Clinical Investigation supports LR09 drug development as a metabolic immune checkpoint inhibitor for the treatment of leukemia Zug, Switzerland, 8 December 2022: Laevoroc Oncology...