News
Recent Highlights
-
Received U.S. Food and Drug Administration (FDA) clearance for the CellFX® System for dermatologic procedures requiring ablation and resurfacing of the skin - Received CE mark approval for the CellFX System
-
Initiated the CellFX System Controlled Launch program in the
U.S. andEurope , including system implementations and completion of the first procedures performed by participating Key Opinion Leader (KOL) aesthetic dermatologists - Continued preparation to make an FDA 510(k) submission for a sebaceous hyperplasia (SH) specific indication for the CellFX System as early as the end of the first quarter of 2021
- Enrolled and treated the first patients in an IDE pivotal comparison study to evaluate the treatment of cutaneous non-genital warts using the CellFX System
“Our diligent efforts throughout 2020 resulted in regulatory clearances for the CellFX System in the
Fourth Quarter 2020 Results
Cash, cash equivalents and investments totaled
Operating expenses for the three months ended
Operating expenses for the twelve months ended
Net loss for the three months ended
Impact of COVID-19
The COVID-19 pandemic had minimal impact on our operations in the fourth quarter of 2020. Product development, execution of clinical trials, regulatory timelines and controlled commercial launch have not been materially affected at this time but due to the uncertain scope and duration of the pandemic, future impact to our operations and financial results cannot be reasonably estimated.
Webcast and Conference Call Information
Pulse Biosciences’ management will host a conference call today,
About
To stay informed about the CellFX System, please visit CellFX.com and sign up for updates.
Forward-Looking Statements
All statements in this press release that are not historical are forward-looking statements, including, among other things, statements relating to Pulse Biosciences’ expectations regarding regulatory clearance and the timing of FDA and other regulatory filings or approvals, including meetings with FDA and the ability of the Company to successfully complete a 510(k) submission for the CellFX System for a SH-specific indication or other dermatologic indications, the ability of the Company to obtain a Medical Device License from
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Condensed Consolidated Balance Sheets |
||||||||
(In thousands, except par value) |
||||||||
(Unaudited) |
||||||||
|
|
|
||||||
2020 |
|
2019 |
||||||
ASSETS |
||||||||
Current assets: |
||||||||
Cash and cash equivalents |
$ |
12,463 |
|
$ |
6,899 |
|
||
Investments |
8,012 |
|
18,499 |
|
||||
Prepaid expenses and other current assets |
1,864 |
|
1,005 |
|
||||
Total current assets |
|
22,339 |
|
|
26,403 |
|
||
Property and equipment, net |
2,478 |
|
2,566 |
|
||||
Intangible assets, net |
3,882 |
|
4,547 |
|
||||
|
2,791 |
|
2,791 |
|
||||
Right-of-use assets |
9,438 |
|
5,114 |
|
||||
Other assets |
365 |
|
494 |
|
||||
Total assets |
$ |
41,293 |
|
$ |
41,915 |
|
||
LIABILITIES AND STOCKHOLDERS’ EQUITY |
||||||||
Current liabilities: |
||||||||
Accounts payable |
$ |
1,717 |
|
$ |
1,963 |
|
||
Accrued expenses |
5,326 |
|
2,496 |
|
||||
Lease liability, current |
542 |
|
— |
|
||||
Total current liabilities |
|
7,585 |
|
|
4,459 |
|
||
Lease liability, less current portion |
|
10,814 |
|
|
6,719 |
|
||
Total liabilities |
|
18,399 |
|
|
11,178 |
|
||
Stockholders’ equity: |
||||||||
Preferred stock, |
— |
|
— |
|
||||
Common stock, |
25 |
|
21 |
|
||||
Additional paid-in capital |
195,410 |
|
153,401 |
|
||||
Accumulated other comprehensive income (loss) |
(1 |
) |
4 |
|
||||
Accumulated deficit |
(172,540 |
) |
(122,689 |
) |
||||
Total stockholders’ equity |
|
22,894 |
|
|
30,737 |
|
||
Total liabilities and stockholders’ equity |
$ |
41,293 |
|
$ |
41,915 |
|
||
|
||||||||||||||||
Condensed Consolidated Statements of Operations and Comprehensive Loss |
||||||||||||||||
(In thousands, except per share data) |
||||||||||||||||
(Unaudited) |
||||||||||||||||
Three-Month Periods Ended |
|
Twelve-Month Periods Ended |
||||||||||||||
|
|
|
||||||||||||||
2020 |
|
2019 |
|
2020 |
|
2019 |
||||||||||
Revenue |
$ |
— |
|
$ |
— |
|
$ |
— |
|
$ |
— |
|
||||
Operating expenses: |
|
|
|
|
|
|
|
|
||||||||
General and administrative |
6,165 |
|
7,174 |
|
22,856 |
|
22,327 |
|
||||||||
Research and development |
7,425 |
|
6,590 |
|
26,444 |
|
24,961 |
|
||||||||
Amortization of intangible assets |
166 |
|
167 |
|
665 |
|
666 |
|
||||||||
Total operating expenses |
|
13,756 |
|
|
13,931 |
|
|
49,965 |
|
|
47,954 |
|
||||
Other income: |
|
|
||||||||||||||
Interest income |
|
6 |
|
|
143 |
|
|
114 |
|
|
983 |
|
||||
Total other income |
|
6 |
|
|
143 |
|
|
114 |
|
|
983 |
|
||||
Net loss |
|
(13,750 |
) |
|
(13,788 |
) |
|
(49,851 |
) |
|
(46,971 |
) |
||||
Other comprehensive loss: |
||||||||||||||||
Unrealized gain (loss) on available-for-sale securities |
(2 |
) |
(4 |
) |
(5 |
) |
5 |
|
||||||||
Comprehensive loss |
$ |
(13,752 |
) |
$ |
(13,792 |
) |
$ |
(49,856 |
) |
$ |
(46,966 |
) |
||||
Net loss per share: |
||||||||||||||||
Basic and diluted net loss per share |
$ |
(0.54 |
) |
$ |
(0.66 |
) |
$ |
(2.14 |
) |
$ |
(2.26 |
) |
||||
Weighted average shares used to compute net loss per common share — basic and diluted |
|
25,360 |
|
|
20,799 |
|
|
23,248 |
|
|
20,746 |
|
||||
|
|
|
|
|
|
|
|
|
|
|
|
|
||||
Three-Month Periods Ended |
|
Twelve-Month Periods Ended |
||||||||||||||
|
|
|
||||||||||||||
Stock Based Compensation Expense: |
2020 |
|
2019 |
|
2020 |
|
2019 |
|||||||||
General and administrative |
$ |
1,333 |
|
$ |
2,585 |
|
$ |
6,062 |
|
$ |
7,466 |
|
||||
Research and development |
1,056 |
|
963 |
|
4,013 |
|
3,821 |
|
||||||||
Total stock-based compensation expense |
$ |
2,389 |
|
$ |
3,548 |
|
$ |
10,075 |
|
$ |
11,287 |
|
View source version on businesswire.com: https://www.businesswire.com/news/home/20210222005820/en/
Investors:
510.241.1077
IR@pulsebiosciences.com
or
415.937.5406
philip@gilmartinir.com
Media:
Nadine D. Tosk
504.453.8344
nadinepr@gmail.com or
press@pulsebiosciences.com
Source: