News
Recent Highlights
-
Nano-Pulse Stimulation™ (NPS™) technology was highlighted in three clinical study presentations demonstrating its high clearance rates of benign skin lesions at the Annual Meeting of the
American Society for Dermatologic Surgery . -
Presented data from a study evaluating the clinical and histologic response of NPS technology in treating challenging cases of nodular Basal Cell Carcinoma at the International
Master Course onAging Skin World Congress . - Completed enrollment in the Company’s CellFX Warts Pivotal Study.
- Obtained ISO-13485:2016 Quality System Management Certification to begin preparations for international commercialization of the CellFX System.
-
Appointed industry veteran
Sandra Gardiner as Executive Vice President and Chief Financial Officer. -
Announced Board approval to pursue a rights offering seeking to raise
$30 million in net proceeds. -
Following receipt of a Not Substantially Equivalent Letter from the
U.S. Food and Drug Administration (FDA) on its previous 510(k) submission, the Company remains engaged with FDA to determine the regulatory path forward for the CellFX System. The Company recently requested a formal Q-submission meeting with FDA to discuss requirements for a new 510(k) submission and based on recent communication, expects the meeting to take place in May.
“I am proud of our continued work to develop NPS technology across multiple clinical applications. We’ve developed a novel and proprietary platform, the CellFX System, that implements a novel utilization-based business model to align incentives between physicians, patients and
Financial Update
Cash, cash equivalents and investments totaled
Operating expenses for the three months ended
Net loss for the fourth quarter ended
About
Caution: Pulse Biosciences’ CellFX System and Nano-Pulse Stimulation (NPS) technology are for investigational use only.
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 filings or approvals including meetings with FDA and the ability of the Company to design studies to produce data for a new 510(k) submission for the CellFX System, the ability of the Company to prepare and provide data to FDA, NPS technology including the effectiveness of such technology, the CellFX System including the benefits of the CellFX System and commercialization of the CellFX System, current and planned future clinical studies and the ability of the Company to execute such studies and results of any such studies, other matters related to its pipeline of product candidates, the Company’s market opportunity, the Company’s ability to raise capital through the rights offering or to consummate the rights offering, the final terms of the rights offering including the offering amount, record date and the subscription price and the related registration statement, future financial performance and other future events. These statements are not historical facts but rather are based on Pulse Biosciences’ current expectations, estimates, and projections regarding Pulse Biosciences’ business, operations and other similar or related factors. Words such as “may,” “will,” “could,” “would,” “should,” “anticipate,” “predict,” “potential,” “continue,” “expects,” “intends,” “plans,” “projects,” “believes,” “estimates,” and other similar or related expressions are used to identify these forward-looking statements, although not all forward-looking statements contain these words. You should not place undue reliance on forward-looking statements because they involve known and unknown risks, uncertainties, and assumptions that are difficult or impossible to predict and, in some cases, beyond Pulse Biosciences’ control. Actual results may differ materially from those in the forward-looking statements as a result of a number of factors, including those described in Pulse Biosciences’ filings with the
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Consolidated Balance Sheets |
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(in thousands, except par value) |
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(unaudited) |
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2019 |
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2018(1) |
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ASSETS |
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Current assets: |
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Cash and cash equivalents |
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$ |
|
6,899 |
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$ |
|
51,103 |
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Investments |
|
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18,499 |
|
|
|
8,480 |
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Prepaid expenses and other current assets |
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1,005 |
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|
779 |
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Total current assets |
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26,403 |
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|
60,362 |
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Property and equipment, net |
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2,566 |
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2,173 |
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Intangible assets, net |
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4,547 |
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|
5,213 |
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||
|
|
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2,791 |
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2,791 |
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Right-of-use assets |
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5,114 |
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— |
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Other assets |
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494 |
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|
101 |
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Total assets |
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$ |
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41,915 |
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$ |
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70,640 |
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LIABILITIES AND STOCKHOLDERS’ EQUITY |
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Current liabilities: |
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Accounts payable |
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$ |
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1,963 |
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$ |
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1,272 |
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Accrued expenses |
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2,496 |
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1,421 |
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Deferred rent, current |
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— |
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|
415 |
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Total current liabilities |
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4,459 |
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3,108 |
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Deferred rent, net of current |
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— |
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1,198 |
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Lease liability |
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6,719 |
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|
— |
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Total liabilities |
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11,178 |
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|
4,306 |
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Stockholders’ equity: |
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Preferred stock, |
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— |
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— |
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Common stock, |
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21 |
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21 |
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Additional paid-in capital |
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153,401 |
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142,032 |
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Accumulated other comprehensive loss |
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4 |
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(1 |
) |
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Accumulated deficit |
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(122,689 |
) |
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(75,718 |
) |
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Total stockholders’ equity |
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30,737 |
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66,334 |
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Total liabilities and stockholders’ equity |
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$ |
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41,915 |
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$ |
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70,640 |
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(1) |
As of |
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Consolidated Statements of Operations and Comprehensive Loss |
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(in thousands, except per share data) |
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(unaudited) |
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Year Ended |
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2019 |
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2018 |
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2017 |
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Revenue |
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$ |
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— |
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$ |
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— |
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$ |
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— |
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Operating expenses: |
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General and administrative |
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22,327 |
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20,045 |
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15,503 |
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Research and development |
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24,961 |
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17,253 |
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9,646 |
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Amortization of intangible assets |
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|
666 |
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|
665 |
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|
665 |
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Total operating expenses |
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47,954 |
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37,963 |
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|
25,814 |
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Other income (expense): |
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Interest income |
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|
983 |
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|
446 |
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247 |
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Other expense |
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— |
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(28 |
) |
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— |
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Total other income |
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983 |
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|
418 |
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|
247 |
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Loss from operations, before income taxes |
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(46,971 |
) |
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(37,545 |
) |
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(25,567 |
) |
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Income tax benefit |
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— |
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— |
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— |
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Net loss |
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(46,971 |
) |
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|
(37,545 |
) |
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(25,567 |
) |
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Other comprehensive loss: |
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Unrealized gain (loss) on available-for-sale securities, net of tax |
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5 |
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50 |
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(44 |
) |
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Comprehensive loss |
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$ |
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(46,966 |
) |
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$ |
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(37,495 |
) |
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$ |
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(25,611 |
) |
Net loss per share: |
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Basic and diluted net loss per share |
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$ |
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(2.26 |
) |
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$ |
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(2.20 |
) |
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$ |
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(1.73 |
) |
Weighted average shares used to compute net loss per common share — basic and diluted |
|
|
20,746 |
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|
|
17,078 |
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|
|
14,754 |
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Year Ended |
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Stock Based Compensation Expense: |
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2019 |
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2018 |
|
2017 |
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General and administrative |
|
$ |
|
7,466 |
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$ |
|
9,004 |
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$ |
|
9,136 |
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Research and development |
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3,821 |
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3,334 |
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|
1,790 |
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Total stock-based compensation expense |
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$ |
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11,287 |
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$ |
|
12,338 |
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$ |
|
10,926 |
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View source version on businesswire.com: https://www.businesswire.com/news/home/20200316005773/en/
Investors:
510.241.1077
IR@pulsebiosciences.com
or
415.937.5406
philip@gilmartinir.com
Media:
Nadine D. Tosk
504.453.8344
press@pulsebiosciences.com
Source: