SAN MATEO, Calif. - Wednesday, 08. May 2024
Total revenues of $752 million in the first quarter, including product
revenue of $747 million, an 82% increase from the prior-year period
BRUKINSA revenue of $489 million, driven by growth in the U.S. and
Europe of 153% and 243%, respectively, from the prior-year period; with
recent fifth FDA approval, BRUKINSA now has the broadest label in the
BTKi class
Rapidly advancing late-stage hematology pipeline;
sonrotoclax in development both as a monotherapy and in combination with
backbone therapy BRUKINSA; pivotal program initiated for BTK CDAC
Progressing potentially differentiated solid tumor programs with ADC,
degrader platforms and targeted therapies in priority cancer types
Significantly improved operating leverage and progress on path to sustainable profitability
(BUSINESS
WIRE) -- BeiGene, Ltd. (NASDAQ: BGNE; HKEX: 06160; SSE: 688235), a
global oncology company, today announced results from the first quarter
2024 and business highlights.
“We are pleased to present another
quarter of strong financial results. Supported by our tremendous global
growth in revenue, we have now ascended into the top 15 of global
oncology innovators based on total oncology sales. We also continue to
make significant improvement in our operating leverage as we progress to
sustainable profitability,” said John V. Oyler, Co-Founder, Chairman
and CEO at BeiGene. “We strengthened our hematology leadership with
BRUKINSA, now the BTK inhibitor with the broadest label in the class, as
we advance our innovative pipeline of therapies for hematologic
malignancies. With TEVIMBRA now approved for use in the U.S. and Europe,
we look forward to rapidly advancing our deep pipeline of solid tumor
therapies to match our leadership in hematology and continue to solidify
our reputation as a global oncology innovator.”
Financial Highlights
(Amounts in thousands of U.S. dollars)
Three Months Ended March 31,
(in thousands, except percentages)
2024
2023
% Change
Net product revenues
$
746,918
$
410,291
82
%
Net revenue from collaborations
$
4,734
$
37,510
(87
)%
Total Revenue
$
751,652
$
447,801
68
%
GAAP loss from operations
$
(261,348
)
$
(371,258
)
(30
)%
Adjusted loss from operations*
$
(147,341
)
$
(275,859
)
(47
)%
*
For an explanation of our use of non-GAAP financial measures refer to
the "Use of Non-GAAP Financial Measures" section later in this press
release and for a reconciliation of each non-GAAP financial measure to
the most comparable GAAP measures, see the table at the end of this
press release.
Key Business Updates
BRUKINSA® (zanubrutinib)
U.S. sales of BRUKINSA totaled $351 million in the first quarter of
2024, representing growth of 153% over the prior-year period, as
BRUKINSA gained share in treatment-naïve (TN) chronic lymphocytic
leukemia (CLL), and emerged as the BTKi class leader in new-patient
share in relapsed or refractory (R/R) CLL; BRUKINSA sales in Europe
totaled $67 million in the first quarter of 2024, representing growth of
243%, driven by continued gains in market share and additional
reimbursements including France, which implemented reimbursement for
BRUKINSA within CLL, Waldenström’s macroglobulinemia (WM) and marginal
zone lymphoma for the first time;
Presented a new matching
adjusted indirect comparison of the efficacy of BRUKINSA versus
acalabrutinib in R/R CLL based on data from the Phase 3 ALPINE and Phase
3 ASCEND trials demonstrating a progression-free survival and Complete
Response (CR) advantage for BRUKINSA versus acalabrutinib, as well as
potentially improved overall survival; and
Received U.S. Food
and Drug Administration (FDA) approval for the treatment of adult
patients with R/R follicular lymphoma, in combination with the anti-CD20
monoclonal antibody obinutuzumab, after two or more lines of systemic
therapy.
TEVIMBRA® (tislelizumab)
Sales of
tislelizumab totaled $145 million in the first quarter of 2024,
representing growth of 26% compared to the prior-year period;
Announced European Commission approval as a treatment for non-small
cell lung cancer (NSCLC) across three indications, including first- and
second-line use;
Received FDA approval for the treatment of second-line esophageal squamous cell carcinoma (ESCC) after prior chemotherapy;
Received FDA acceptance of BLA for the treatment of first-line gastric or gastroesophageal junction cancers; and
The pending FDA approval for tislelizumab in first-line unresectable,
recurrent, locally advanced, or metastatic ESCC with a target PDUFA
action date of July 2024 may be deferred on account of a potential delay
in scheduling clinical site inspections.
Key Pipeline Highlights
Hematology
Sonrotoclax (BCL2 inhibitor)
Received FDA fast track designation for R/R mantle cell lymphoma (MCL); and
Continued enrollment in R/R MCL and WM with registrational intent as
well as Phase 3 in TN CLL in combination with BRUKINSA; more than 850
patients enrolled to date across the program.
BGB-16673 (BTK CDAC)
Initiated expansion cohorts in R/R MCL (potential registrational
intent) and R/R CLL; more than 220 patients enrolled to date across the
program; and
Expect to initiate Phase 3 clinical trial in R/R CLL by the end of 2024.
Solid Tumors
Lung Cancer
Enrolled last subject in a Phase 3 clinical trial for ociperlimab (anti-TIGIT) for first-line PD-L1 high NSCLC;
Multiple tislelizumab lung cancer combination cohorts with BGB-A445
(anti-OX40), LBL-007 (anti-LAG3) and BGB-15025 (HPK1 inhibitor) expected
to read out in 2024; and
Pan-KRAS and MTA-cooperative PRMT5 inhibitors and EGFR CDAC on track to enter the clinic in the second half of 2024.
Breast Cancer
BGB-43395 (CDK4 inhibitor): Initiated fourth dose level of monotherapy,
which is in the efficacious dose range with no dose limiting toxicities
observed; and initiated dosing of combination with fulvestrant just
over four months from first monotherapy dose.
BG-68501 (CDK2
inhibitor): Initiated second dose level of monotherapy in first-in-human
study, with clinical pharmacokinetics as expected and no dose limiting
toxicities observed.
BG-C9074 (B7H4 ADC): First patient dosed in Australia in global first-in-human Phase 1 study.
Gastrointestinal Cancers
Multiple tislelizumab combination cohorts with LBL-007 (anti-LAG3) and BGB-A445 (anti-OX40) reading out in 2024;
Plan to submit a BLA with the NMPA for zanidatamab for the treatment of second-line biliary tract cancer; and
CEA-ADC and FGFR2b-ADC on track to enter the clinic in the second half of 2024.
Other Business Highlights
The U.S. Patent and Trademark Office (USPTO) granted the Company’s
petition for post-grant review of the Pharmacyclics’ patent asserted
against the Company in a patent infringement suit, stating that the
Company has shown that it is more likely than not that the patent is
invalid; The USPTO is expected to issue a final decision on the validity
of the patent within 12 months;
Published the 2023
Responsible Business & Sustainability Report which details the
Company’s commitment to providing equitable benefit to patients,
business and society; and
Anticipate opening of
state-of-the-art biologics manufacturing facility and clinical R&D
center at the Princeton West Innovation Campus in Hopewell, New Jersey,
in July.
First Quarter 2024 Financial Highlights
Revenue
for the three months ended March 31, 2024, was $752 million, compared to
$448 million in the same period of 2023, driven primarily by growth in
BRUKINSA product sales in the U.S. and Europe of 153% and 243%
respectively.
Product Revenue for the three months ended March
31, 2024, was $747 million, compared to $410 million in the same period
of 2023, representing an increase of 82%. The increase in product
revenue was attributable to increased sales of our internally developed
products, BRUKINSA and tislelizumab. For the three months ended March
31, 2024, the U.S. was the Company’s largest market, with product
revenue of $351 million, compared to $139 million in the prior year
period.
Gross Margin as a percentage of global product revenue
for the first quarter of 2024 was 83%, compared to 80% in the prior-year
period. The gross margin percentage increased primarily due to
proportionally higher sales mix of global BRUKINSA compared to other
products in the portfolio.
Operating Expenses
GAAP
Non-GAAP
(in thousands, except percentages)
Q1 2024
Q1 2023
% Change
Q1 2024
Q1 2023
% Change
Research and development
$
460,638
$
408,584
13
%
$
405,440
$
361,696
12
%
Selling, general and administrative
$
427,427
$
328,499
30
%
$
372,146
$
283,154
31
%
Amortization
$
—
$
187
(100
)%
$
—
$
—
NM
Total operating expenses
$
888,065
$
737,270
20
%
$
777,586
$
644,850
21
%
Research
and Development (R&D) Expenses increased for the first quarter of
2024 compared to the prior-year period on both a GAAP and adjusted basis
primarily due to advancing preclinical programs into the clinic and
early clinical programs into late stage. Upfront fees and milestone
payments related to in-process R&D for in-licensed assets totaled
$35 million in the first quarter of 2024, compared to nil in the
prior-year period.
Selling, General and Administrative (SG&A)
Expenses increased for the first quarter of 2024 compared to the
prior-year period on both a GAAP and adjusted basis due to continued
investment in the global commercial launch of BRUKINSA, primarily in the
U.S. and Europe. SG&A expenses as a percentage of product sales
were 57% for the first quarter of 2024 compared to 80% in the prior year
period.
Loss from Operations in the first quarter of 2024
decreased 30% on a GAAP basis and 47% on an adjusted basis compared to
the prior-year period. The decrease is driven by significantly improved
operating leverage associated with substantial revenue growth and
expense discipline as we make significant progress on the path to
sustainable profitability.
GAAP Net Loss improved for the quarter
ended March 31, 2024, compared to the prior-year period, as our product
revenue growth and management of expenses is driving increased
operating leverage.
For the quarter ended March 31, 2024, net
loss per share was $(0.19) and $(2.41) per American Depositary Share
(ADS), compared to $(0.26) per share and $(3.34) per ADS in the prior
year period.
Cash Used in Operations for the quarter ended March
31, 2024, totaled $309 million compared to $564 million in the
prior-year period, driven by improved operating leverage.
For
further details on BeiGene’s First Quarter 2024 Financial Statements,
please see BeiGene’s Quarterly Report on Form 10-Q for the first quarter
of 2024 filed with the U.S. Securities and Exchange Commission.
About BeiGene
BeiGene
is a global oncology company that is discovering and developing
innovative treatments that are more affordable and accessible to cancer
patients worldwide. With a broad portfolio, we are expediting
development of our diverse pipeline of novel therapeutics through our
internal capabilities and collaborations. We are committed to radically
improving access to medicines for far more patients who need them. Our
growing global team of more than 10,000 colleagues spans five
continents. To learn more about BeiGene, please visit www.beigene.com
and follow us on LinkedIn, X (formerly known as Twitter) and Facebook.
Forward-Looking Statements
This
press release contains forward-looking statements within the meaning of
the Private Securities Litigation Reform Act of 1995 and other federal
securities laws, including statements regarding BeiGene’s ability to
advance its pipeline of therapies for hematologic malignancies and
rapidly advance its pipeline of solid tumor therapies to solidify its
reputation as a global oncology innovator; BeiGene’s anticipated
clinical activities and read outs; the opening date of BeiGene’s
biologics manufacturing facility and clinical R&D center in
Hopewell, New Jersey; BeiGene’s progress towards sustainable
profitability; and BeiGene’s plans, commitments, aspirations and goals
under the caption “About BeiGene”. Actual results may differ materially
from those indicated in the forward-looking statements as a result of
various important factors, including BeiGene’s ability to demonstrate
the efficacy and safety of its drug candidates; the clinical results for
its drug candidates, which may not support further development or
marketing approval; actions of regulatory agencies, which may affect the
initiation, timing and progress of clinical trials and marketing
approval; BeiGene’s ability to achieve commercial success for its
marketed medicines and drug candidates, if approved; BeiGene's ability
to obtain and maintain protection of intellectual property for its
medicines and technology; BeiGene’s reliance on third parties to conduct
drug development, manufacturing, commercialization, and other services;
BeiGene’s limited experience in obtaining regulatory approvals and
commercializing pharmaceutical products; BeiGene’s ability to obtain
additional funding for operations and to complete the development of its
drug candidates and achieve and maintain profitability; and those risks
more fully discussed in the section entitled “Risk Factors” in
BeiGene’s most recent quarterly report on Form 10-Q, as well as
discussions of potential risks, uncertainties, and other important
factors in BeiGene’s subsequent filings with the U.S. Securities and
Exchange Commission. All information in this press release is as of the
date of this press release, and BeiGene undertakes no duty to update
such information unless required by law.
Condensed Consolidated Statements of Operations (U.S. GAAP)
(Amounts in thousands of U.S. dollars, except for shares, American Depositary Shares (ADSs), per share and per ADS data)
Three Months Ended
March 31,
2024
2023
(Unaudited)
Revenues
Product revenue, net
$
746,918
$
410,291
Collaboration revenue
4,734
37,510
Total revenues
751,652
447,801
Cost of sales - products
124,935
81,789
Gross profit
626,717
366,012
Operating expenses:
Research and development
460,638
408,584
Selling, general and administrative
427,427
328,499
Amortization of intangible assets
—
187
Total operating expenses
888,065
737,270
Loss from operations
(261,348
)
(371,258
)
Interest income, net
16,160
16,016
Other income (expense), net
1,762
18,303
Loss before income taxes
(243,426
)
(336,939
)
Income tax expense
7,724
11,492
Net loss
(251,150
)
(348,431
)
Net loss per share, basic and diluted
$
(0.19
)
$
(0.26
)
Weighted-average shares outstanding—basic and diluted
1,355,547,626
1,354,164,760
Net loss per ADS, basic and diluted
$
(2.41
)
$
(3.34
)
Weighted-average ADSs outstanding—basic and diluted
104,272,894
104,166,520
Select Condensed Consolidated Balance Sheet Data (U.S. GAAP)
(Amounts in thousands of U.S. Dollars)
As of
March 31,
December 31,
2024
2023
(unaudited)
(audited)
Assets:
Cash, cash equivalents, restricted cash and short-term investments
$
2,807,436
$
3,188,584
Accounts receivable, net
435,294
358,027
Inventories
447,345
416,122
Property, plant and equipment, net
1,417,992
1,324,154
Total assets
5,667,681
5,805,275
Liabilities and equity:
Accounts payable
356,575
315,111
Accrued expenses and other payables
569,438
693,731
R&D cost share liability
225,530
238,666
Debt
1,025,992
885,984
Total liabilities
2,307,320
2,267,948
Total equity
$
3,360,361
$
3,537,327
Note Regarding Use of Non-GAAP Financial Measures
BeiGene
provides certain non-GAAP financial measures, including Adjusted
Operating Expenses and Adjusted Operating Loss and certain other
non-GAAP income statement line items, each of which include adjustments
to GAAP figures. These non-GAAP financial measures are intended to
provide additional information on BeiGene’s operating performance.
Adjustments to BeiGene’s GAAP figures exclude, as applicable, non-cash
items such as share-based compensation, depreciation and amortization.
Certain other special items or substantive events may also be included
in the non-GAAP adjustments periodically when their magnitude is
significant within the periods incurred. BeiGene maintains an
established non-GAAP policy that guides the determination of what costs
will be excluded in non-GAAP financial measures and the related
protocols, controls and approval with respect to the use of such
measures. BeiGene believes that these non-GAAP financial measures, when
considered together with the GAAP figures, can enhance an overall
understanding of BeiGene’s operating performance. The non-GAAP financial
measures are included with the intent of providing investors with a
more complete understanding of the Company’s historical and expected
financial results and trends and to facilitate comparisons between
periods and with respect to projected information. In addition, these
non-GAAP financial measures are among the indicators BeiGene’s
management uses for planning and forecasting purposes and measuring the
Company’s performance. These non-GAAP financial measures should be
considered in addition to, and not as a substitute for, or superior to,
financial measures calculated in accordance with GAAP. The non-GAAP
financial measures used by the Company may be calculated differently
from, and therefore may not be comparable to, non-GAAP financial
measures used by other companies.
RECONCILIATION OF SELECTED GAAP MEASURES TO NON-GAAP MEASURES
(in thousands, except per share amounts)
(unaudited)
Three Months Ended
March 31,
2024
2023
( in thousands)
Reconciliation of GAAP to adjusted cost of sales - products:
GAAP cost of sales - products
$
124,935
$
81,789
Less: Depreciation
2,345
2,180
Less: Amortization of intangibles
1,183
799
Adjusted cost of sales - products
$
121,407
$
78,810
Reconciliation of GAAP to adjusted research and development:
GAAP research and development
$
460,638
$
408,584
Less: Share-based compensation expenses
38,045
34,028
Less: Depreciation
17,153
12,860
Adjusted research and development
$
405,440
$
361,696
Reconciliation of GAAP to adjusted selling, general and administrative:
GAAP selling, general and administrative
$
427,427
$
328,499
Less: Share-based compensation expenses
50,669
41,360
Less: Depreciation
4,612
3,985
Adjusted selling, general and administrative
$
372,146
$
283,154
Reconciliation of GAAP to adjusted operating expenses
GAAP operating expenses
$
888,065
$
737,270
Less: Share-based compensation expenses
88,714
75,388
Less: Depreciation
21,765
16,845
Less: Amortization of intangibles
—
187
Adjusted operating expenses
$
777,586
$
644,850
Reconciliation of GAAP to adjusted loss from operations:
GAAP loss from operations
$
(261,348
)
$
(371,258
)
Plus: Share-based compensation expenses
88,714
75,388
Plus: Depreciation
24,110
19,025
Plus: Amortization of intangibles
1,183
986
Adjusted loss from operations
$
(147,341
)
$
(275,859
)
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Contacts
Investor
Liza Heapes
+1 857-302-5663
ir@beigene.com
Media
Kyle Blankenship
+1 667-351-5176
media@beigene.com
