PLx Pharma Inc. (NASDAQ: PLXP) (“PLx” or the “Company”), is a
commercial-stage drug delivery platform technology company focused
on its clinically-validated and patent-protected PLxGuard™ that has
the potential to improve the absorption of many drugs currently on
the market and to reduce the risk of stomach injury associated with
certain drugs. The Company, with its lead products VAZALORE 81 mg
and VAZALORE 325 mg liquid-filled aspirin capsules (referred to
together as “VAZALORE®”), announced today certain financial and
operational results for the three months ended March 31, 2022.
“Our solid base of VAZALORE users continues to
grow, and feedback from consumers and healthcare professionals is
overwhelmingly positive,” said Natasha Giordano, PLx’s President
& CEO. “We continuously evaluate the feedback, along with
market research and other data, and have refined our marketing
efforts.”
Giordano continued, “We are intensifying our
focus to more strongly differentiate VAZALORE from the limitations
of other aspirins. VAZALORE provides fast, predictable absorption
and was designed to help protect the gastroduodenal lining. We are
executing enhanced messaging and some unique programs to increase
trial and conversion among a broader community of consumers and
healthcare professionals.”
Select Business Highlights of First Quarter
2022 and Recent Key Accomplishments
Progress in Building Brand Awareness and Trial
of VAZALORE:
- Retail consumption data for the
most recent 13-week period showed steady growth of VAZALORE in a
declining Heart Health category.1
- Feedback from
healthcare professionals (HCPs) and consumers is overwhelmingly
positive.
- HCPs recognize
VAZALORE as an innovative aspirin therapy, and how important it is
for their secondary prevention patients to achieve the antiplatelet
benefit of aspirin in a reliable and consistent way every day.
- Consumer
sentiment of VAZALORE centers on the following themes: easy to
swallow, did not upset my stomach, and effective for pain
relief.
- The Company’s
cardiovascular care specialists are implementing new VAZALORE
sampling and patient-use survey programs to drive physician
adoption and consumer trial.
- A manuscript of
recently reported pharmacokinetic/pharmacodynamic results on
VAZALORE 81 mg has been submitted to a journal for publication and
is under review.
- The study was led
by Drs. Franchi and Angiolillo from the University of Florida
titled, Pharmacokinetic and Pharmacodynamic Profile of PL-ASA, a
Novel Phospholipid-Aspirin Complex Liquid Formulation, Compared to
Enteric-coated Aspirin at an 81 mg Dose – Results from a
Prospective, Randomized Crossover Study, was a randomized,
open-label, crossover pharmacokinetic and pharmacodynamic study in
healthy volunteers.
- As expected and
consistent with earlier studies at 325 mg, compared to
enteric-coated aspirin VAZALORE 81 mg provided faster and more
complete absorption after a single dose, with earlier and more
potent inhibition of platelet aggregation.
- Cardiovascular thought leaders held
a virtual town hall meeting on March 28, 2022, titled “Aspirin in
2022: A New Aspirin for a New Chapter” as a public health service
to help clarify aspirin therapy in secondary prevention of cardiac
events and dual anti-platelet therapy (DAPT) for the practicing
clinician.
First Quarter 2022 Financial
Highlights
Total revenues for the first quarter of 2022
were $2.1 million, compared to no revenue in the first quarter of
2021. On a sequential basis, net sales increased approximately 31%
compared to the fourth quarter of 2021 and reflected shipments to
retailers in conjunction with strong promotion and display support
during National Heart Health month in February. Net sales of the 81
mg dose (consisting of a 12 count and 30 count SKU), represented
approximately 79% of total net sales in the first quarter of
2022.
Gross margin of 44% was in-line sequentially
with the fourth quarter of 2021 and reflected a favorable product
mix consisting of higher sales of VAZALORE 81 mg.
Total operating expenses were $19.1 million
during the first quarter of 2022, compared to operating expenses of
$3.6 million for the prior year period, and reflected increased
promotional activities and expenses associated with the commercial
launch of VAZALORE during the third quarter of 2021. On a
sequential basis, first quarter operating expenses declined 11%
compared to the fourth quarter of 2021, primarily due to a
strategic reduction in spending on the Company’s national
television advertising campaign.
Research and development expenses declined
approximately 32% to $0.7 million in the first quarter of 2022,
compared to approximately $1 million in first quarter of 2021. The
decrease reflected the non-recurrence of the prior year costs for
pre-commercial manufacturing-related activities such as validation
and optimization work for VAZALORE.
Selling, marketing and administrative expenses
totaled $18.5 million in the first quarter of 2022, compared to
$2.6 million in the prior year period, primarily due to higher
sales and marketing expenses associated with the commercial launch
of VAZALORE. The higher year-over-year expense also included a new
cardiovascular specialty field force and national media television
campaign, which were launched during the third quarter of 2021.
Non-cash stock-based compensation was $1.1 million, compared to
$0.6 million in the first quarter of 2021.
Other income (expense), net totaled $7.4 million
of other income during the first quarter of 2022, compared to other
expense of $7.9 million in the first quarter of 2021. The increase
is largely attributable to the non-cash change in fair value of
warrant liability, primarily due to the fluctuation of the price of
the Company’s common stock.
Net loss attributable to common stockholders for
the first quarter of 2022 was $10.8 million, or a loss of ($0.39)
per diluted share, compared to a net loss of $11.9 million, or
($0.73) per diluted share in the prior year period.
Adjusted non-GAAP net loss per diluted share was
($0.66) in the first quarter of 2022, compared to an adjusted net
loss of ($0.22) per diluted share in the first quarter of 2021.
See table for reconciliation of GAAP to adjusted
non-GAAP net loss per diluted share.
Liquidity
As of March 31, 2022, the Company had $52.5
million in cash and cash equivalents, $0.7 million in accounts
receivable and zero debt on its balance sheet.
1 Nielsen, Single entity Heart Health Aspirin
xAOC; 13-week period ended 3/26/22 versus 13-week period ended
1/1/22.
2022 First Quarter Conference
Call
The Company’s 2022 first quarter conference call
with analysts and investors will be held today at 8:30am ET and may
be accessed by dialing 1-866-394-2901, or if international,
1-616-548-5567, using Conference ID number 4037188. A live audio
webcast of the conference call, along with the earnings press
release and supplemental financial disclosures, will also be
available on the Investor Relations section of the Company's
website at https://ir.plxpharma.com/investor-relations. The webcast
will be available for replay after the call for a period of at
least 30 days.
About VAZALOREVAZALORE is an
FDA-approved liquid-filled aspirin capsule, available in 81 mg and
325 mg doses. VAZALORE delivers aspirin differently from plain and
enteric coated aspirin products. The special complex inside the
capsule is designed for targeted release of aspirin, limiting its
direct contact with the stomach. VAZALORE delivers fast, reliable
absorption for pain relief plus the lifesaving benefits of aspirin.
To learn more about VAZALORE, please visit www.vazalore.com.
About PLx Pharma Inc.PLx Pharma
Inc. is a commercial-stage drug delivery platform technology
company focused on improving how and where active pharmaceutical
ingredients (APIs) are absorbed in the gastrointestinal (GI) tract
via its clinically validated and patent protected PLxGuard™
technology. PLx believes this platform has the potential to improve
the absorption of many drugs currently on the market or in
development, and to reduce the risk of stomach injury associated
with certain drugs. To learn more about PLx Pharma Inc. and its
pipeline, please visit www.plxpharma.com.
Forward-Looking Statements Any
statements made in this press release relating to future financial
or business performance, conditions, plans, prospects, trends, or
strategies and other financial and business matters, including
without limitation, the prospects for commercializing or selling
any products or drug candidates, are forward-looking statements
within the meaning of the Private Securities Litigation Reform Act
of 1995. In addition, when or if used in this press release, the
words “may,” “could,” “should,” “anticipate,” “believe,”
“estimate,” “expect,” “intend,” “plan,” “predict” and similar
expressions and their variants, as they relate to PLx may identify
forward-looking statements. PLx cautions that these forward-looking
statements are subject to numerous assumptions, risks, and
uncertainties, which change over time. Important factors that may
cause actual results to differ materially from the results
discussed in the forward-looking statements or historical
experience include risks and uncertainties, including risks
relating to PLx’s ability to successfully further commercialize its
VAZALORE products; the failure by PLx to secure and maintain
relationships with collaborators; risks relating to clinical
trials; risks relating to the commercialization, if any, of PLx’s
proposed product candidates (such as marketing, regulatory, product
liability, supply, competition, and other risks); dependence on the
efforts of third parties; dependence on intellectual property;
developments and projections relating to our competitors or our
industry; and risks that PLx may lack the financial resources and
access to capital to fund proposed operations. Further information
on the factors and risks that could affect PLx’s business,
financial condition and results of operations are contained in
PLx’s filings with the U.S. Securities and Exchange
Commission (“SEC”), which are available at www.sec.gov. Other
risks and uncertainties are more fully described in PLx’s Form 10-K
for the year ended December 31, 2021, filed with the SEC on March
11, 2022, and in other filings that PLx has made or will make going
forward. These forward-looking statements represent PLx’s estimate
as of the date hereof only, and PLx specifically disclaims any duty
or obligation to update forward-looking statements.
Non-GAAP Measures
PLx’s management considers adjusted non-GAAP net
loss and adjusted non-GAAP net loss per basic and diluted earnings
per share to be important financial indicators of operating
performance, providing investors and analysts with useful measures
of operating results unaffected by the impact on the financial
statements of the volatility of the change in the fair value of the
warrant liability and non-cash and non-recurring dividends and
beneficial conversion features on our preferred stock. Management
uses adjusted non-GAAP net loss and adjusted non-GAAP net loss per
share when analyzing performance. Adjusted non-GAAP net loss and
adjusted non-GAAP net loss per share should be considered in
addition to, but not in lieu of net loss or net loss per share
reported under GAAP.
CONTACTS:Janet M. BarthVice President, Investor
Relations & Corporate Communications, PLx Pharma Inc.(973)
409-6542IR@PLxPharma.com
Lisa M. WilsonFounder & President, In-Site Communications,
Inc.(212) 452-2793lwilson@insitecony.com
Source: PLx Pharma Inc.
PLx Pharma Inc. |
|
UNAUDITED CONSOLIDATED BALANCE SHEETS |
|
(in thousands, except share and per share data) |
|
|
|
|
|
|
|
March 31,2022 |
|
December 31,2021 |
|
ASSETS |
|
|
|
|
CURRENT ASSETS |
|
|
|
|
Cash and cash equivalents |
$ |
52,499 |
|
|
$ |
69,392 |
|
|
Accounts receivable |
|
698 |
|
|
|
634 |
|
|
Inventory, net |
|
3,839 |
|
|
|
2,458 |
|
|
Prepaid expenses and other current assets |
|
712 |
|
|
|
992 |
|
|
TOTAL CURRENT ASSETS |
|
57,748 |
|
|
|
73,476 |
|
|
NON-CURRENT ASSETS |
|
|
|
|
Property and equipment, net |
|
828 |
|
|
|
858 |
|
|
Right of use assets |
|
204 |
|
|
|
230 |
|
|
Goodwill |
|
2,061 |
|
|
|
2,061 |
|
|
Security deposit |
|
17 |
|
|
|
17 |
|
|
TOTAL ASSETS |
$ |
60,858 |
|
|
$ |
76,642 |
|
|
|
|
|
|
|
LIABILITIES, SERIES A AND SERIES B CONVERTIBLE PREFERRED STOCK AND
STOCKHOLDERS' EQUITY |
|
|
|
|
CURRENT LIABILITIES |
|
|
|
|
Accounts payable and accrued liabilities |
$ |
12,716 |
|
|
$ |
10,600 |
|
|
Accrued bonuses |
|
394 |
|
|
|
1,163 |
|
|
Other current liabilities |
|
120 |
|
|
|
116 |
|
|
TOTAL CURRENT LIABILITIES |
|
13,230 |
|
|
|
11,879 |
|
|
NON-CURRENT LIABILITIES |
|
|
|
|
Warrant liability |
|
5,410 |
|
|
|
12,818 |
|
|
Accrued dividends |
|
129 |
|
|
|
129 |
|
|
Other liabilities |
|
106 |
|
|
|
136 |
|
|
TOTAL LIABILITIES |
|
18,875 |
|
|
|
24,962 |
|
|
|
|
|
|
|
Series A convertible preferred stock: $0.001 par value; liquidation
value of $12,642,000; 45,000 shares authorized, 12,642 issued and
outstanding at March 31, 2022 and December 31, 2021 |
|
13,708 |
|
|
|
13,708 |
|
|
Series B convertible preferred stock: $0.001 par value; liquidation
value of $2,492,722; 25,000 shares authorized, 2,364 issued and
outstanding at March 31, 2022 and December 31, 2021 |
|
2,306 |
|
|
|
2,306 |
|
|
|
|
|
|
|
STOCKHOLDERS' EQUITY |
|
|
|
|
Preferred stock; $0.001 par value; 930,000 shares authorized; none
issued and outstanding |
|
- |
|
|
|
- |
|
|
Common stock; $0.001 par value; 100,000,000 shares authorized;
27,539,229 shares issued and outstanding at March 31, 2022 and
December 31, 2021 |
|
28 |
|
|
|
28 |
|
|
Additional paid-in capital |
|
185,000 |
|
|
|
183,912 |
|
|
Accumulated deficit |
|
(159,059 |
) |
|
|
(148,274 |
) |
|
TOTAL STOCKHOLDERS' EQUITY |
|
25,969 |
|
|
|
35,666 |
|
|
TOTAL LIABILITIES, SERIES A AND SERIES B CONVERTIBLE PREFERRED
STOCK AND STOCKHOLDERS' EQUITY |
$ |
60,858 |
|
|
$ |
76,642 |
|
|
PLx Pharma Inc. |
|
UNAUDITED CONSOLIDATED STATEMENTS OF
OPERATIONS |
|
(in thousands, except share and per share data) |
|
|
|
|
|
|
|
Three Months Ended |
|
|
March 31, |
|
|
|
2022 |
|
|
|
2021 |
|
|
REVENUES: |
|
|
|
|
Net sales |
$ |
2,083 |
|
|
$ |
- |
|
|
TOTAL REVENUES |
|
2,083 |
|
|
|
- |
|
|
|
|
|
|
|
Cost of sales |
|
1,169 |
|
|
|
- |
|
|
GROSS PROFIT |
|
914 |
|
|
|
- |
|
|
|
|
|
|
|
OPERATING EXPENSES: |
|
|
|
|
Research and development |
|
654 |
|
|
|
959 |
|
|
Selling, marketing and administrative |
|
18,456 |
|
|
|
2,636 |
|
|
TOTAL OPERATING EXPENSES |
|
19,110 |
|
|
|
3,595 |
|
|
OPERATING LOSS |
|
(18,196 |
) |
|
|
(3,595 |
) |
|
|
|
|
|
|
OTHER INCOME (EXPENSE): |
|
|
|
|
Interest income (expense), net |
|
3 |
|
|
|
(10 |
) |
|
Change in fair value of warrant liability |
|
7,408 |
|
|
|
(7,935 |
) |
|
TOTAL OTHER INCOME (EXPENSE) |
|
7,411 |
|
|
|
(7,945 |
) |
|
LOSS BEFORE INCOME TAXES |
|
(10,785 |
) |
|
|
(11,540 |
) |
|
Income taxes |
|
- |
|
|
|
- |
|
|
NET LOSS |
|
(10,785 |
) |
|
|
(11,540 |
) |
|
|
|
|
|
|
Preferred dividends |
|
- |
|
|
|
(322 |
) |
|
NET LOSS ATTRIBUTABLE TO COMMON STOCKHOLDERS |
$ |
(10,785 |
) |
|
$ |
(11,862 |
) |
|
|
|
|
|
|
Net loss per common share - basic and diluted |
$ |
(0.39 |
) |
|
$ |
(0.73 |
) |
|
|
|
|
|
|
Weighted average shares of common shares - basic and diluted |
|
27,539,229 |
|
|
|
16,361,583 |
|
|
PLx Pharma Inc. |
|
RECONCILIATION OF GAAP TO ADJUSTED NON-GAAP NET LOSS
ATTRIBUTABLE TO COMMON STOCKHOLDERS AND ADJUSTED NON-GAAP EARNINGS
PER SHARE |
(in thousands, except share and per share data) |
|
|
|
|
|
|
Three Months Ended |
|
|
March 31, |
|
|
|
2022 |
|
|
|
2021 |
|
|
Net loss attributable to common stockholders - GAAP |
$ |
(10,785 |
) |
|
$ |
(11,862 |
) |
|
Adjustments: |
|
|
|
|
Change in fair value of warrant liability |
|
(7,408 |
) |
|
|
7,935 |
|
|
Preferred dividends |
|
- |
|
|
|
322 |
|
|
Adjusted non-GAAP net loss attributable to common stockholders |
$ |
(18,193 |
) |
|
$ |
(3,605 |
) |
|
|
|
|
|
|
Adjusted non-GAAP net loss per common share - basic and
diluted |
$ |
(0.66 |
) |
|
$ |
(0.22 |
) |
|
|
|
|
|
|
Weighted average shares of common shares - basic and diluted |
|
27,539,229 |
|
|
|
16,361,583 |
|
|
|
|
|
|
|
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