$38.1M in Rubraca® (rucaparib) global net product revenues for Q1 2021, down 11% vs. Q1 2020, due to continued headwinds from COVID-19 in the US and Europe
Maintained US market share as US PARP inhibitor market impacted by COVID-19
Imaging and treatment INDs cleared by FDA for FAP-2286, a novel peptide-targeted radionuclide therapy (PTRT)
Phase 1/2 LuMIERE study of FAP-2286 expected to open for enrollment this quarter
Top-line data from Phase 3 ATHENA trial of Rubraca as first-line maintenance treatment for ovarian cancer monotherapy anticipated 2H 2021
$190.9M in cash and cash equivalents and $61.4M in available funding under the ATHENA financing at March 31, 2021, anticipated to fund the Company’s operating plan into early 2023 based on current revenue and expense forecasts
$28.1M reduction in R&D and SG&A expense and 25% reduction in net cash used in operating activities compared to Q1 2020
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