Protalix BioTherapeutics reported revenues from selling goods of $3.6 million and revenues from license and R&D services of $7.3 million for the second quarter ended June 30, 2020. The company also announced positive topline results in its BRIDGE phase III clinical trial of PRX-102 for the treatment of Fabry disease and subsequent BLA submission to the U.S. Food and Drug Administration (FDA).
Announced positive top-line data in its Phase III BRIDGE study of PRX-102 for the Treatment of Fabry disease.
Submitted a Biologics License Application (BLA) to the U.S. Food and Drug Administration for PRX-102 for the treatment of Fabry disease.
Revenues from selling goods increased by 6% compared to the same period of 2019.
Cash and cash equivalents at June 30, 2020 was $4.8 million, with $35.2 million in bank deposits.
Protalix is continuing to build for the long term and look forward to continuing to execute as they move towards the anticipated commercial launch of PRX-102 for the treatment of Fabry disease.