BioCryst Pharmaceuticals, Inc. (Nasdaq: BCRX) today reported
financial results for the fourth quarter and full year ended
December 31, 2023, and provided a corporate update.
“The impressive growth we are seeing with
ORLADEYO has put us in a position to accelerate our path to
profitability while continuing to invest in our diverse pipeline of
first-in-class or best-in-class molecules that we believe will
deliver our next marketed product,” said Jon Stonehouse, president
and chief executive officer of BioCryst.
Program Updates and Key
Milestones
ORLADEYO®
(berotralstat): Oral, Once-daily Treatment for Prevention
of Hereditary Angioedema (HAE)
Attacks
- ORLADEYO net revenue in the fourth
quarter of 2023 was $90.9 million.
- The total number of U.S. patients
on paid or long-term free product reached 1,104 at the end of the
fourth quarter (+30 percent y-o-y) with 71.5 percent of those
patients on paid product.
- Net U.S. patient growth totaled 321
in 2023, including new patients still on short-term quick start
product at the end of the quarter.
- The number of new ORLADEYO
prescribers in the fourth quarter of 2023 (Q4 2023) was the largest
number of new prescribers of any quarter in 2023.
- Real-world data presented at the
American Academy of Allergy, Asthma & Immunology (AAAAI) annual
meeting reinforced prior data showing patients switching to
ORLADEYO experience sustained attack reduction regardless of
baseline attack rate or prior HAE prophylaxis treatment.
- Access to ORLADEYO continues to
expand to more HAE patients around the world. In Q4 2023, ORLADEYO
was approved in Argentina, launched in Spain, and granted final
pricing approval in Austria. In the first quarter of 2024, ORLADEYO
secured final reimbursement in Italy.
“As the real-world evidence with ORLADEYO
consistently underscores, patients are switching to ORLADEYO
because they can achieve outstanding HAE attack control and
tolerability with an oral, once-daily therapy, leading to
life-changing results,” said Charlie Gayer, chief commercial
officer of BioCryst.
Fourth Quarter 2023 Financial
Results
For the three months ended December 31, 2023,
total revenues were $93.4 million, compared to $79.5 million in the
fourth quarter of 2022. The increase was primarily due to $90.9
million in ORLADEYO net revenue in the fourth quarter of 2023,
compared to $70.7 million in the fourth quarter of 2022. Revenue in
the fourth quarter of 2023 also included $2.3 million of net
revenue from RAPIVAB related sales, compared to $8.7 million in the
fourth quarter of 2022.
Research and development (R&D) expenses for
the fourth quarter of 2023 decreased to $70.1 million from $73.2
million in the fourth quarter of 2022 (-4 percent year-over-year),
primarily due to the discontinuation of the BCX9930 and BCX9250
programs announced in December 2022 and November 2022,
respectively. These reductions were partially offset by increased
investment in BCX17725 and our other early-stage programs,
including the $5 million upfront payment to Clearside Biomedical
related to avoralstat, and ORLADEYO label expansion and life cycle
investments, such as our ongoing ORLADEYO pediatric trial.
Selling, general and administrative (SG&A)
expenses for the fourth quarter of 2023 increased to $64.4 million,
compared to $50.2 million in the fourth quarter of 2022 (+28
percent year-over-year). The increase was primarily due to
increased investment to expand and enhance the U.S. commercial team
and international operations.
Interest expense was $24.6 million in the fourth
quarter of 2023, compared to $26.5 million in the fourth quarter of
2022. The decrease was primarily due to a decrease in the
amortization of interest associated with our royalty financing
obligations, partially offset by an increase in interest expense
associated with the Pharmakon debt refinancing secured in April
2023.
Net loss for the fourth quarter of 2023 was
$61.7 million, or $0.31 per share, compared to a net loss of $71.5
million, or $0.38 per share, for the fourth quarter of 2022.
Non-GAAP net loss for the fourth quarter of 2023 was $56.4 million,
or $0.28 per share when excluding one-time costs associated with
the R&D restructuring and the postponement of the expansion at
our Discovery Center in Alabama, totaling $5.4 million. A
reconciliation between GAAP and non-GAAP net loss is provided in
the table below.
Cash, cash equivalents, restricted cash and
investments totaled $390.8 million as of December 31, 2023,
compared to $443.9 million as of December 31, 2022. Net cash
utilization for the fourth quarter of 2023 was $8.6 million.
Full Year 2023 Financial
Results
For the full year ended December 31, 2023, total
revenues were $331.4 million, compared to $270.8 million in the
full year ended December 31, 2022. The increase was primarily due
to $326.0 million of ORLADEYO net revenue in 2023, compared to
$251.6 million in 2022. The increase in ORLADEYO net revenue was
partially offset by a decrease in other net revenues of $13.8
million, primarily due to RAPIVAB stockpiling sales to complete the
U.S. Department of Health and Human Services procurement contract
during the year ended December 31, 2022.
R&D expenses in full year 2023 decreased to
$216.6 million from $253.3 million in full year 2022 (-14 percent
year-over-year), primarily due to the discontinuation of the
BCX9930 and BCX9250 programs announced in December 2022 and
November 2022, respectively. These reductions were partially offset
by increased investment in BCX17725, increased investment in our
other early-stage discovery programs, including the $5 million
upfront payment to Clearside Biomedical related to avoralstat,
ORLADEYO label expansion and life cycle investments, such as our
ongoing ORLADEYO pediatric trial, and an increase in indirect costs
to support our programs.
SG&A expenses in full year 2023 increased to
$213.9 million, compared to $159.4 million in full year 2022 (+34
percent year-over-year). The increase was primarily due to
increased investment in order to expand and enhance the U.S.
commercial team and expanded international operations.
Interest expense was $108.2 million in full year
2023, compared to $99.1 million in full year 2022. The increase in
interest expense was primarily associated with the interest accrued
on the Tranche A Loan of $300.0 million under the Pharmakon
Loan Agreement.
Other expense was comprised primarily of a loss
on extinguishment of debt of $29.0 million on the repayment of
the term loans under the Athyrium Credit Agreement and net foreign
currency losses of $1.0 million, partially offset by interest
income of $15.8 million for the year ended December 31, 2023.
Other income was comprised of interest income of $5.1 million,
partially offset by net foreign currency losses of $2.0 million for
the year ended December 31, 2022.
Net loss for full year 2023 was $226.5 million,
or $1.18 per share, compared to a net loss of $247.1 million, or
$1.33 per share, for full year 2022. Non-GAAP net loss for full
year 2023 was $192.2 million, or $1.00 per share when excluding the
one-time loss on debt extinguishment of $29.0 million on the
repayment of the term loans under the Athyrium Credit Agreement
recognized in the second quarter of 2023, as well as the R&D
restructuring and the postponement of previously planned capital
expenditures at our Discovery Center in Alabama recognized in the
fourth quarter of 2023, totaling $5.4 million. A reconciliation
between GAAP and non-GAAP net loss is provided in the table
below.
Non-GAAP Pro forma Financial
Measures
The information furnished in this release
includes non-GAAP pro forma financial measures that differ from
measures calculated in accordance with generally accepted
accounting principles in the United States of America (“GAAP”),
including financial measures labeled as “non-GAAP” or
“adjusted.”
We believe providing these non-GAAP measures,
which show our pro forma results with these items adjusted, is
valuable and useful since they allow the company and investors to
better understand the company’s financial performance in the
absence of these one-time events and allowed investors to more
accurately understand our 2023 results and more easily compare them
to future results. These non-GAAP pro forma measures also
correspond with the way we expect investors and financial analysts
to compare our results. Our non-GAAP pro forma measures should be
considered only as supplements to, and not as substitutes for or in
isolation from, our other measures of financial information
prepared in accordance with GAAP, such as GAAP revenue, operating
income, net income, and earnings per share.
Our references to our fourth quarter 2023 and
full year 2023 “non-GAAP pro forma” financial measures of adjusted
net loss and adjusted earnings per share constitute non-GAAP
financial measures. They refer to our GAAP results, adjusted to
show the results without the one-time loss on debt extinguishment
on the repayment of the term loans under the Athyrium Credit
Agreement, as well as the R&D restructuring and the
postponement of previously planned capital expenditures at our
Discovery Center in Alabama. A reconciliation between GAAP and
non-GAAP net loss is provided in the table below.
Financial Outlook for 2024
The company expects full year 2024 global net
ORLADEYO revenue to be between $380 million and $400 million. The
general pattern of revenue throughout 2024 is expected to be
similar to past years, with the seasonal impact of prescription
reauthorizations and the potential impact of the Inflation
Reduction Act in the first quarter driving a quarter-over-quarter
revenue decline in the first quarter, followed by a strong return
to growth in the second quarter.
The company expects full year 2024 operating
expenses to be between $365 million and $375 million, flat to
expected full year 2023 operating expenses. The company now expects
that R&D expenses in 2024 will be reduced by between $20
million and $30 million versus 2023. SG&A expenses are expected
to increase by $20 million in 2024, primarily to support the
continued U.S. and global growth of ORLADEYO to $1 billion in peak
sales.
This operating expense outlook does not reflect
non-cash stock compensation expense, or one-time expenses related
to the previously announced workforce reduction implemented in the
first quarter of 2024.
Based on the company’s disciplined approach to
capital allocation, and the revenue expected from ORLADEYO, the
company expects to achieve a full-year operating profit in 2024
(not including non-cash stock compensation), be approaching
quarterly positive earnings per share (EPS) and positive cash flow
in the second half of 2025 (not including non-cash stock
compensation), and be profitable on an EPS basis, with positive
cash flow, for full year 2026. The company expects it can achieve
these financial milestones without raising additional funds and
does not intend to draw the additional $150 million of debt
available to it from Pharmakon.
Conference Call and Webcast
BioCryst management will host a conference call
and webcast at 8:30 a.m. ET today to discuss the financial results
and provide a corporate update. The live call may be accessed by
dialing 1-844-481-2942 for domestic callers and 1-412-317-1866 for
international callers. A live webcast and replay of the call will
be available online in the investors section of the company website
at www.biocryst.com.
About BioCryst Pharmaceuticals
BioCryst Pharmaceuticals is a global biotechnology company with a
deep commitment to improving the lives of people living with
complement-mediated and other rare diseases. BioCryst leverages its
expertise in structure-guided drug design to develop first-in-class
or best-in-class oral small-molecule and protein therapeutics to
target difficult-to-treat diseases. BioCryst has commercialized
ORLADEYO® (berotralstat), the first oral, once-daily plasma
kallikrein inhibitor, and is advancing a pipeline of small-molecule
and protein therapies. For more information, please visit
www.biocryst.com or follow us on LinkedIn.
Forward-Looking StatementsThis
press release contains forward-looking statements, including
statements regarding future results, performance or achievements.
These statements involve known and unknown risks, uncertainties and
other factors which may cause BioCryst’s actual results,
performance or achievements to be materially different from any
future results, performance or achievements expressed or implied by
the forward-looking statements. These statements reflect our
current views with respect to future events and are based on
assumptions and are subject to risks and uncertainties. Given these
uncertainties, you should not place undue reliance on these
forward-looking statements. Some of the factors that could affect
the forward-looking statements contained herein include: BioCryst’s
ability to successfully implement its commercialization plans for
ORLADEYO, which could take longer or be more expensive than
planned; risks related to the reduction in size of BioCryst’s
R&D organization; the results of BioCryst’s partnerships with
third parties may not meet BioCryst’s current expectations; risks
related to government actions, including that decisions and other
actions, including as they relate to pricing, may not be taken when
expected or at all, or that the outcomes of such decisions and
other actions may not be in line with BioCryst’s current
expectations; the commercial viability of ORLADEYO, including its
ability to achieve market acceptance; ongoing and future
preclinical and clinical development of product candidates may take
longer than expected and may not have positive results; the FDA or
other applicable regulatory agency may require additional studies
beyond the studies planned for products and product candidates, may
not provide regulatory clearances which may result in delay of
planned clinical trials, may impose certain restrictions, warnings,
or other requirements on products and product candidates, may
impose a clinical hold with respect to product candidates, or may
withhold, delay or withdraw market approval for products and
product candidates; product candidates, if approved, may not
achieve market acceptance; BioCryst’s ability to successfully
commercialize its products and product candidates; BioCryst’s
ability to successfully manage its growth and compete effectively;
risks related to the international expansion of BioCryst’s
business; timing for achieving profitability and positive cash flow
may not meet management’s expectations; statements and projections
regarding financial guidance and goals and the attainment of such
goals may differ from actual results based on market factors and
BioCryst’s ability to execute its operational and budget plans; and
actual financial results may not be consistent with expectations,
including that revenue, operating expenses and cash usage may not
be within management's expected ranges. Please refer to the
documents BioCryst files periodically with the Securities and
Exchange Commission, specifically BioCryst’s most recent Annual
Report on Form 10-K, Quarterly Reports on Form 10-Q, and Current
Reports on Form 8-K, which identify important factors that could
cause actual results to differ materially from those contained in
BioCryst’s projections and forward-looking statements.
BCRXW
Contact:John Bluth+1 919 859
7910jbluth@biocryst.com
BIOCRYST PHARMACEUTICALS, INC. |
CONSOLIDATED FINANCIAL SUMMARY |
(In thousands, except per share) |
|
Statements of Operations (unaudited) |
|
|
Three Months EndedDecember 31, |
|
Twelve Months EndedDecember 31, |
|
|
2023 |
|
|
|
2022 |
|
|
|
2023 |
|
|
|
2022 |
|
Revenues: |
|
|
|
|
|
|
|
ORLADEYO |
$ |
90,883 |
|
|
$ |
70,735 |
|
|
$ |
325,990 |
|
|
$ |
251,633 |
|
Other |
|
2,518 |
|
|
|
8,810 |
|
|
|
5,422 |
|
|
|
19,194 |
|
Total revenues |
|
93,401 |
|
|
|
79,545 |
|
|
|
331,412 |
|
|
|
270,827 |
|
|
|
|
|
|
|
|
|
Expenses: |
|
|
|
|
|
|
|
Cost of product sales |
|
1,557 |
|
|
|
2,383 |
|
|
|
4,481 |
|
|
|
6,408 |
|
Research and development |
|
70,052 |
|
|
|
73,207 |
|
|
|
216,566 |
|
|
|
253,297 |
|
Selling, general and administrative |
|
64,382 |
|
|
|
50,153 |
|
|
|
213,894 |
|
|
|
159,371 |
|
Royalty |
|
80 |
|
|
|
113 |
|
|
|
180 |
|
|
|
186 |
|
Total operating expenses |
|
136,071 |
|
|
|
125,856 |
|
|
|
435,121 |
|
|
|
419,262 |
|
|
|
|
|
|
|
|
|
Loss from operations |
|
(42,670 |
) |
|
|
(46,311 |
) |
|
|
(103,709 |
) |
|
|
(148,435 |
) |
|
|
|
|
|
|
|
|
Interest and other income |
|
4,465 |
|
|
|
2,704 |
|
|
|
15,777 |
|
|
|
5,127 |
|
Interest expense |
|
(24,583 |
) |
|
|
(26,458 |
) |
|
|
(108,239 |
) |
|
|
(99,092 |
) |
Loss on extinguishment of
debt |
|
— |
|
|
|
— |
|
|
|
(29,019 |
) |
|
|
— |
|
Foreign currency losses,
net |
|
(374 |
) |
|
|
(1,400 |
) |
|
|
(1,039 |
) |
|
|
(1,983 |
) |
Loss before income taxes |
$ |
(63,162 |
) |
|
$ |
(71,465 |
) |
|
$ |
(226,229 |
) |
|
$ |
(244,383 |
) |
Income tax (benefit)
expense |
|
(1,431 |
) |
|
|
76 |
|
|
|
310 |
|
|
|
2,733 |
|
Net loss |
$ |
(61,731 |
) |
|
$ |
(71,541 |
) |
|
$ |
(226,539 |
) |
|
$ |
(247,116 |
) |
|
|
|
|
|
|
|
|
Basic and diluted net loss per
common share |
$ |
(0.31 |
) |
|
$ |
(0.38 |
) |
|
$ |
(1.18 |
) |
|
$ |
(1.33 |
) |
|
|
|
|
|
|
|
|
Weighted average shares
outstanding |
|
201,409 |
|
|
|
186,922 |
|
|
|
192,198 |
|
|
|
185,908 |
|
Balance
Sheet Data (in thousands) |
|
|
December 31, 2023(unaudited) |
|
December 31, 2022(Note 1) |
Cash, cash equivalents and investments |
$ |
388,987 |
|
|
$ |
442,387 |
|
Restricted cash |
|
1,804 |
|
|
|
1,472 |
|
Receivables |
|
56,950 |
|
|
|
50,599 |
|
Total assets |
|
516,960 |
|
|
|
550,000 |
|
Secured term loan |
|
303,231 |
|
|
|
231,624 |
|
Royalty financing
obligation |
|
531,599 |
|
|
|
501,655 |
|
Accumulated deficit |
|
(1,681,159 |
) |
|
|
(1,454,620 |
) |
Stockholders’ deficit |
|
(455,528 |
) |
|
|
(294,597 |
) |
Shares of common stock
outstanding |
|
205,771 |
|
|
|
187,906 |
|
|
|
|
|
Note 1: Derived from audited
financial statements |
|
|
|
Reconciliation of Adjusted Net Income and Adjusted Diluted
Earnings Per Share (in thousands) |
|
|
Three Months EndedDecember 31, |
|
Twelve Months EndedDecember 31, |
|
|
2023 |
|
|
|
2022 |
|
|
|
2023 |
|
|
|
2022 |
|
GAAP net
loss |
$ |
(61,731 |
) |
|
$ |
(71,541 |
) |
|
$ |
(226,539 |
) |
|
$ |
(247,116 |
) |
Less: One-time loss on
extinguishment of Athyrium term loans |
|
— |
|
|
|
— |
|
|
|
(29,019 |
) |
|
|
— |
|
Less: One-time R&D
restructuring expense |
|
(3,380 |
) |
|
|
— |
|
|
|
(3,380 |
) |
|
|
— |
|
Less: One-time cost associated
with expensing previously capitalized costs due to postponement of
Discovery Center (AL) expansion |
|
(1,988 |
) |
|
|
— |
|
|
|
(1,988 |
) |
|
|
— |
|
Adjusted net
loss |
$ |
(56,363 |
) |
|
$ |
(71,541 |
) |
|
$ |
(192,152 |
) |
|
$ |
(247,116 |
) |
|
|
|
|
|
|
|
|
GAAP basic and diluted
net loss per common share |
$ |
(0.31 |
) |
|
$ |
(0.38 |
) |
|
$ |
(1.18 |
) |
|
$ |
(1.33 |
) |
|
|
|
|
|
|
|
|
Adjusted basic and
diluted net loss per common share |
$ |
(0.28 |
) |
|
$ |
(0.38 |
) |
|
$ |
(1.00 |
) |
|
$ |
(1.33 |
) |
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