FDA Fast Track Designation for Lunresertib in Combination with Zedoresertib for Genomic-Defined Platinum-Resistant Ovarian Cancer
“The FDA’s decision to grant Fast Track designation for this combination therapy validates our synthetic lethality approach to treating high-unmet-need cancers,” said Esteban Rodrigo Imedio, Executive Medical Director, Oncology, Debiopharm. “Coming immediately after Dr. Yap’s presentation of the MYTHIC data at AACR, this designation highlights the potential of combining lunresertib and zedoresertib to provide a meaningful new clinical option for patients with biomarker-selected ovarian cancer who have exhausted platinum-based therapies.”
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