American PARP inhibitor specialist Clovis Oncology (Nasdaq: CLVS) will present four posters related to the Rubraca (rucaparib) development program at the 2018 European Society of Medical Oncology congress.
Clovis will present initial results from the Phase II TRITON2 clinical trial in advanced mCRPC, data from which formed the basis for the recently-granted US Food and Drug Administration Breakthrough Designation in this indication.
The Boulder, Colorado-based firm will also provide genomic profiling data from patients who were screened following progression on prior therapy for enrollment in TRITON2 or the Phase III TRITON3 study.
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