Pulse Biosciences reported a GAAP net loss of $18.6 million for the first quarter of 2021, compared to a net loss of $11.9 million for the same period in the prior year. The company's cash, cash equivalents and investments totaled $59.9 million as of March 31, 2021, compared to $20.5 million as of December 31, 2020. The company onboarded the first 15 participating U.S. and European aesthetic specialty practices in the first quarter for CellFX® System Controlled Launch program.
Commenced the CellFX® System Controlled Launch program and onboarded the first 15 participating U.S. and European aesthetic specialty practices in the first quarter
Submitted anticipated final response to Health Canada regarding the CellFX System Medical Device License
Received FDA IDE approval for a feasibility study to assess the treatment of basal cell carcinoma using the CellFX System
Continued patient enrollment and treatments in an FDA IDE approved pivotal comparison study to assess the treatment of cutaneous non-genital warts using the CellFX System; 51 of 150 patients have been enrolled to date
Pulse Biosciences is focused on the commercial launch of the CellFX System and expanding its applications outside of aesthetic dermatology.