Retrophin's first quarter 2020 financial results showed net product sales increased to $47.8 million compared to $39.6 million for the same period in 2019. The company achieved the critical milestone of enrolling the first 190 patients in its pivotal DUPLEX Study of sparsentan in FSGS. Net income for the first quarter of 2020 was $0.8 million, compared to a net loss of $41.0 million for the same period in 2019.
Phase 3 DUPLEX Study of sparsentan in FSGS achieved enrollment of the first 190 patients required to support the 36-week proteinuria analysis.
The pivotal PROTECT Study of sparsentan in IgA nephropathy (IgAN) continues enrollment toward 280 patients required to enable the 36-week proteinuria analysis for accelerated approval submissions
Suzanne L. Bruhn, Ph.D., joined the Board of Directors.
Net product sales for the first quarter of 2020 were $47.8 million, compared to $39.6 million for the same period in 2019
Retrophin continues to believe that top-line efficacy data from the 36-week proteinuria endpoint analysis in the first quarter of 2021 are achievable for DUPLEX study. For PROTECT Study, the company continues to believe that top-line efficacy data from the 36-week proteinuria endpoint analysis in the first half of 2022 are achievable.
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