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Pulse Biosciences Reports First Quarter 2022 Financial Results

HAYWARD, Calif.--(BUSINESS WIRE)-- Pulse Biosciences, Inc. (Nasdaq: PLSE), a novel bioelectric medicine company commercializing the CellFX® System powered by

articlePulse Biosciences, IncMay 11, 20224/company/pulse-biosciences-inc/news/pulse-biosciences-reports-first-quarter-2022-financial-results-2022-05-11
Pulse Biosciences Reports First Quarter 2022 Financial Results

About this update from Pulse Biosciences, Inc

[{"type":"text","content":" HAYWARD, Calif.--(BUSINESS WIRE)--\nPulse Biosciences, Inc. (Nasdaq: PLSE), a novel bioelectric medicine company commercializing the CellFX® System powered by Nano-Pulse Stimulation™ (NPS™) technology, today announced financial results for the first quarter of 2022.\nThis press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20220511005989/en/(Graphic: Business Wire)\nCompany Updates\n\n\nIncreased the overall CellFX System commercial session utilization four week moving average1 during Q1 with decreasing trend in early Q2 due to transition in commercial strategy.\n\n\nAppointed new commercial leadership and began initiation of the CellFX System utilization program in May with nine commercial clinics to establish commercial integration best practices. Established program goal for each clinic of 40 commercial sessions per month. Average monthly utilization of the nine participating clinics during Q1 was 14 sessions per month.\n\n\nGenerated first quarter 2022 revenue of $444 thousand.\n\n\nCompleted one commercial sale of a CellFX System in the first quarter of 2022.\n\n\nTransitioned 10 Controlled Launch Program participants to commercial use in the first quarter totaling 39 commercial conversions at the end of the first quarter. There are 20 clinics remaining in the Controlled Launch program after a total of 11 clinics have opted out as of the end of Q1.\n\n\nMet with FDA regarding the Additional Information (AI) letter response to the sebaceous hyperplasia 510(k). Provided additional analysis of the clinical data following the meeting, at FDA’s request, and anticipate further communication prior to any formal response to the AI letter.\n\n\n1 Utilization is measured as commercial sessions defined as individual patient treatments, regardless of the number of lesions treated, performed using CellFX Systems that have been purchased or converted to commercial use from the controlled launch program.\n\n“In the first quarter of 2022 we took steps to refocus our CellFX dermatology efforts by bringing in new commercial leadership. We have prioritized increasing CellFX System utilization at a subset of our commercial clinics, with the goal of developing commercial integration best practices that will drive utilization across all clinics. While these best practices are being established t...

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