SINOVAC BIOTECH LTD.
No. 39 Shangdi Xi Rd, Haidian District
Indicate by check mark whether the registrant files or will file annual
reports under cover of Form 20-F or Form 40-F:
Pursuant to the requirements of the Securities
Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
Exhibit 99.1
SINOVAC
Reports Unaudited and Unreviewed Second Half of 2025 Financial Results and Files 2025
Annual Report on Form 20-F
BEIJING,
China, June 5, 2026 /Business Wire/ -- Sinovac Biotech Ltd. (NASDAQ: SVA) (“SINOVAC” or the “Company”), a leading
provider of biopharmaceutical products in China, today announced it filed its annual report on Form 20-F for the fiscal year ended December
31, 2025 (the “Annual Report”) with the U.S. Securities and Exchange Commission. An electronic copy of the Annual Report
can be accessed at the Company’s website at www.sinovac.com.cn or www.sinovac.com and at the SEC’s website
www.sec.gov.
The Company
also announced its unaudited and unreviewed financial results for the second half of 2025 and audited financial results for the full year
ended December 31, 2025.
Second
Half and Full Year of 2025 Financial Summary
| ● | Sales
for the six months ended December 31, 2025 were $255.7 million, compared to $232.7 million in the prior year period. |
| ● | Sales
in 2025 were $386.0 million, compared to $361.4 million in the prior year. |
| ● | The
Company posted $38.0 million of net loss attributable to common shareholders, or a loss of $0.53 per basic and diluted share, in the
six months ended December 31, 2025, compared to net loss attributable to common shareholders of $2.9 million, or a loss of $0.04 per
basic and diluted share, in the prior year period. |
| ● | The
Company posted $59.7 million of net loss attributable to common shareholders, or a loss of $0.83 per basic and diluted share in 2025,
compared to net income attributable to common shareholders of $90.9 million, or an income of $1.27 per basic and diluted share, in the
prior year. |
Mr. Weidong Yin, CEO of SINOVAC, commented, “In 2025, SINOVAC
continued to advance its corporate strategy with a strong focus on globalization. I’m encouraged that our overseas business has
emerged as a primary growth driver, significantly contributing to our full-year sales. While international expansion remains our core
focus, our research and development (“R&D”) continues to yield positive progress. Notably, our tetanus vaccine was approved
for commercial launch in 2025. Targeting hospital clinics and emergency departments, this product successfully expands our commercial
footprint beyond the network of Centers for Disease Control and Prevention. Furthermore, we have multiple key vaccines nearing late-stage
approval, which will further support our global growth potential in the coming years.”
Robust Overseas Growth and Resilient Chinese Mainland Market
In 2025, the Company’s globalization strategy delivered significant
progress. The Company’s overseas business maintained robust growth, offsetting a slight decrease in Chinese domestic sales. For
the full year 2025, sales from overseas markets surged to $124.8 million, representing a year-over-year increase of 93.9%. Consequently,
the contribution of overseas sales to the Company’s total top line almost doubled from 17.8% in 2024 to 32.3% in 2025.
The growth of overseas sales was driven by several core products. Notably,
the supply of the varicella vaccine demonstrated strong commercial achievement overseas, with full-year sales increasing nearly ninefold.
Furthermore, the supply of the Enterovirus Type 71 (EV71) vaccine progressed steadily outside the Chinese Mainland, with overseas sales
nearly doubling. The sales of the trivalent influenza vaccine also delivered solid performance, quadrupling its overseas sales year over
year. This momentum was fueled by deepened market penetration and landmark commercial breakthroughs in emerging markets. The Company was
the exclusive winner of the Chilean influenza vaccine global tender for both 2025 and 2026. Additionally, SINOVAC signed two Product Development
Partnership agreements with the Brazilian Ministry of Health for local production and a 10-year supply commitment, laying a solid foundation
for its long-term presence in Latin America.
In the Chinese Mainland market, despite intensifying
competition and moderating demand, the sales of our key proprietary products, including the EV71 vaccine, hepatitis A vaccine and quadrivalent
influenza vaccine remained stable. Meanwhile, domestic sales for the poliomyelitis vaccine, trivalent influenza vaccine and varicella
vaccine experienced varying degrees of decline, primarily due to reduced procurement volume under the Chinese Mainland public market.
Strategic Pipeline Advancement Toward Commercialization
In 2025, the Company accelerated the advancement
of its R&D pipeline, forming a clear and tiered portfolio. To date, the Company has one new product approved for market launch, two
product candidates under marketing authorization application review, and four product candidates that have entered or are preparing to
enter Phase III clinical trials. Meanwhile, two major candidates based on mRNA technology are being studied in the clinical stage. The
advancement of these pipeline projects will serve as a vital engine driving the Company’s long-term growth potential. The key near-term
pipeline products include:
Lyophilized Rabies Vaccine (Serum-Free
Vero Cell) (PVRV-SF): Expected to be the first rabies vaccine in the Chinese Mainland market with a serum-free and
animal-origin-free component process, this product candidate is currently under marketing application review and is anticipated to
be approved for launch by July 2026. The Company is concurrently pursuing its WHO prequalification application and conducting
international Phase III clinical trials overseas, accelerating the global deployment of this candidate.
Bivalent Enterovirus Vaccine (HFMD2):
As the world’s first bivalent HFMD vaccine candidate under Phase III clinical trial evaluation, the Company successfully obtained
primary endpoint data and monitoring data from the first epidemic season in March 2026. Preliminary results indicate that the vaccine
candidate exhibits a favorable safety profile and satisfactory efficacy results.
13-Valent Pneumococcal Conjugate Vaccine
(PCV13): The Phase III clinical trial for this product candidate is progressing smoothly. We expect to complete all clinical trials
and file the marketing authorization application within 2026. Additionally, the Company obtained clinical trial approval from the Philippine
regulatory authority in April 2026 and plans to conduct an infant PCV13 trial enrolling participants aged approximately 2 months (42 to
89 days) to support global regulatory applications.
Quadrivalent Enterovirus Vaccine (HFMD4):
Following favorable safety and immunogenicity results observed in the Phase II clinical trial of this vaccine candidate, its Phase III
clinical trial was initiated in June 2026. As the world’s first quadrivalent HFMD vaccine candidate to reach this stage, it covers
the major pathogenic serotypes and is expected to significantly reduce both the incidence of HFMD and the risk of severe HFMD cases.
Group ACYW135 Meningococcal Conjugate Vaccine (MCV4): The Company is developing an MCV4 vaccine candidate leveraging its bacterial vaccine platform. Phase
III clinical trials for this product candidate were officially initiated in March 2026.
Fully Human Anti-Tetanus Toxin Monoclonal Antibody (HmAb-TT):
Beyond the core vaccine portfolio, the Company is developing an innovative monoclonal antibody candidate for the emergency prophylaxis
of tetanus. As the Company’s first self-developed monoclonal antibody candidate in this segment, Phase II clinical results have
demonstrated a favorable safety profile, as well as antibody levels significantly higher than those of tetanus immunoglobulin currently
available. Following these positive findings, the Phase III clinical trial for HmAb-TT is scheduled to officially initiate in June 2026.
Unaudited
and Unreviewed Financial Results for the Second Half of 2025
Sales in
the second half of 2025 were $255.7 million compared to $232.7 million in the prior year period. Export markets led this expansion, posting
a 144.3% increase primarily driven by higher procurement of varicella vaccines.
Cost of
sales decreased to $75.2 million in the second half of 2025 from $81.5 million in the prior year period. The decrease was mainly due to lower expenses recognized in connection with the long-term employee incentive plan established
in 2022 (the “Employee Incentive Plan”).
Gross profit
in the second half of 2025 increased to $180.5 million from $151.1 million in the prior year period. Gross profit margin increased from
65.0% in the second half of 2024 to 70.6% in the second half of 2025, primarily driven by the expansion of international sales with higher
gross profit.
Selling,
general and administrative expenses in the second half of 2025 were $185.8 million, compared to $212.3 million in the prior year period.
The decrease was mainly due to lower expenses recognized in connection with the Employee Incentive
Plan.
Research
and development expenses in the second half of 2025 were $89.3 million, a decrease from $128.3 million in the prior year period. The decrease
was mainly due to lower expenses recognized in connection with the Employee Incentive Plan.
Loss on
disposal and impairment of property, plant and equipment (“PP&E”) in the second half of 2025 was $135.4 million, compared
to $25.0 million in the prior year period. This was because the Company identified impairment indicators on certain of its machinery,
equipment, construction in progress and leasehold improvements and a drop in the lease market price of certain plants located in Hangzhou
and Beijing, and recorded impairment of PP&E.
Other income,
net in the second half of 2025 was $46.7 million, a decrease from $233.0 million in the prior year period. The change was mainly due to
a decrease in investment income earned from investment products issued by financial institutions, and net foreign exchange loss reflecting
fluctuations in foreign exchange rates.
Net loss
in the second half of 2025 was $102.3 million, compared to a net loss of $18.3 million in the prior year period.
Net loss
attributable to common shareholders was $38.0 million, or a loss of $0.53 per basic and diluted share, in the second half of 2025, compared
to a loss attributable to common shareholders of $2.9 million, or a loss of $0.04 per basic and diluted share, in the prior year period.
In 2018,
11,800,000 common shares (the “2018 PIPE Shares”) were issued pursuant to the Securities Purchase Agreement dated July 2,
2018. The validity of this share issuance has been subject to dispute. Whether these shares may be excluded from the Company’s issued
and outstanding common shares is contingent upon the outcome of certain legal proceedings pending in Antigua. Excluding the 2018 PIPE
Shares, the basic and diluted weighted average number of the Company’s common stock outstanding would be 60,060,702. On that
basis, the basic and diluted net loss per share for the second half of 2025 would be $0.63, compared to basic and diluted net loss per
share of $0.05 in the prior year period.
The Company’s
financial statements for the second half of 2025 are prepared and presented in accordance with U.S. GAAP. However, they have not been
audited or reviewed by the Company’s independent registered public accounting firm.
Financial
Results for the Year Ended December 31, 2025
Sales in
2025 were $386.0 million compared to $361.4 million in the prior year. The increase was primarily driven by higher sales of varicella
vaccines and influenza vaccines resulting from increased procurement by international customers, partially offset by a decline in sIPV
vaccine sales due to lower domestic birth rates.
Cost of
sales decreased to $124.0 million in 2025 from $140.7 million in 2024. The decrease was mainly due to lower expenses recognized in connection
with the Employee Incentive Plan, and our ongoing efforts in cost reduction and efficiency improvement.
Gross profit
increased to $262.0 million in 2025 from $220.7 million in the prior year. Gross profit margin increased from 61.1% in 2024 to 67.9% in
2025, primarily driven by a favorable shift in product and channel mix toward higher-margin international sales, as well as improved cost
efficiencies in production.
Selling,
general and administrative expenses in 2025 were $333.0 million, compared to $420.9 million in the prior year. The decrease was mainly
due to lower expenses recognized in connection with the Employee Incentive Plan.
Research
and development expenses in 2025 were $216.2 million, a decrease from $270.7 million in the prior year. The decrease was mainly due to lower expenses recognized in connection with the Employee Incentive Plan.
Loss on
disposal and impairment of PP&E and intangible assets, and loss on impairment of goodwill in 2025 was $202.8 million, compared to
$30.3 million in the prior year. This was because the Company identified impairment indicators on certain of its machinery, equipment,
construction in progress and leasehold improvements and a drop in the lease market price of certain plants located in Hangzhou and Beijing,
and recorded impairment of $137.6 million of PP&E. In addition, the Company recorded impairment of $65.5 million of in-process research
and development assets and goodwill generated during the acquisition of a subsidiary that produces
rabies vaccines. The Company identified impairment indicators, including fierce competition, delayed vaccine market launch, and changes
in product positioning in 2025.
Other
income, net in 2025 was $208.6 million, a decrease from $527.6 million in the prior year, which primarily consisted of (i)
investment income of $307.4 million and $482.1 million in 2025 and 2024, respectively, earned from investment products issued by
financial institutions; and (ii) a net foreign exchange loss of $109.8 million in 2025 and a net foreign exchange gain of $61.4
million in 2024, resulting from fluctuations in foreign exchange rates.
Net loss
in 2025 was $198.8 million, compared to a net income of $40.7 million in the prior year.
Net loss
attributable to common shareholders was $59.7 million, or a loss of $0.83 per basic and diluted share in 2025, compared to an income attributable
to common shareholders of $90.9 million, or an income of $1.27 per basic and diluted share, in the prior year.
Excluding
the 2018 PIPE Shares, the basic and diluted weighted average number of the Company’s common shares outstanding would be 60,060,702.
On that basis, the basic and diluted net loss per share in 2025 would be $0.99, compared to basic and diluted net income per share of
$1.51 in the prior year.
As of December
31, 2025, cash and cash equivalents and restricted cash totaled $1.2 billion, compared to $602.2 million as of December 31, 2024. The
increase was mainly due to the increased net cash inflow of investing activities, which was mainly attributable to the maturity and sales
of investment products issued by financial institutions. In 2025, net cash used in operating activities was $512.2 million, mainly reflecting
the tax payments made during the year and decline in cash collections from sales; net cash provided by investing activities was $4.4 billion,
mainly reflecting the net position of debt and equity securities maturity and sales over purchases; and net cash used in financing activities
was $3.4 billion, mainly reflecting the payment of dividends.
In 2025,
$20.9 million (RMB145.8 million) in dividends was declared and paid by Sinovac Biotech Co., Ltd. (“Sinovac Beijing”)
and Sinovac (Dalian) Vaccine Technology Co., Ltd. (“Sinovac Dalian”) to
their respective minority shareholders. $55.7 million (RMB389.3 million) in dividends was declared and paid by such subsidiaries to Sinovac
Holding Group Co., Ltd. (“Sinovac Beijing Holding”) in 2025. Additionally, the Company’s
board of directors had declared a special cash dividend of $55.00 per common share with total $3,958.2 million in April 2025,
of which $3,300.3 million in dividends was paid by Sinovac Antigua to its shareholders in 2025, and $657.9 million was retained as deferred
dividend payment to Sinovac Antigua’s shareholders, mainly holding 2018 PIPE Shares.
Subsequent
Events
In 2026, $88.0 million (RMB600.0 million) in dividends
was declared and paid by Sinovac Beijing, and Sinovac Dalian, of which $24.4 million (RMB166.5 million) was declared and paid to their
respective minority shareholders, and $63.6 million (RMB433.5 million) in dividends was declared and paid by such subsidiaries to Sinovac
Beijing Holding.
About
SINOVAC
Sinovac Biotech Ltd. (SINOVAC) is a China-based
global biopharmaceutical company, with a mission of “supply vaccines to eliminate human diseases”. The Company specializes
in the research, development, manufacturing and commercialization of vaccines and related biological products that protect against human
infectious diseases.
The Company’s diversified portfolio includes
vaccines for influenza, viral hepatitis, varicella, Hand-Foot-Mouth disease (HFMD), poliomyelitis, pneumococcal disease, etc., of which
3 vaccines have been prequalified by WHO, including inactivated hepatitis A vaccine Healive®, Sabin-strain inactivated
polio vaccine (sIPV), and varicella vaccine.
SINOVAC has a leading edge in developing vaccines
to combat infectious disease outbreaks and was among the first to initiate R&D during major public health emergencies, including
SARS, H5N1, H1N1, and COVID-19. The Company developed the world’s first inactivated SARS vaccine (Phase I completed), China’s
first H5N1 influenza vaccine (Panflu®), the world’s first H1N1 influenza vaccine (Panflu.1®), and
CoronaVac®, the most widely used inactivated COVID-19 vaccine globally.
Beyond its marketed portfolio, the Company is
advancing a robust pipeline that includes combination vaccines, recombinant protein vaccines and next-generation platforms such as mRNA
technologies and antibodies.
With a long-standing commitment to innovation
and global health, SINOVAC is expanding its global footprint by strengthening partnerships with research institutions, international organizations,
and local partners. Through broader market presence, technological cooperation, and localized production, the Company aims to accelerate
vaccine development and supply, enhance regional access to high-quality products, and better address unmet medical needs while improving
preparedness for future pandemics.
For more information, please see the Company’s
website at www.sinovac.com.cn or www.sinovac.com.
Safe
Harbor Statement
This announcement contains forward-looking statements
within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended, and as defined in the U.S. Private Securities Litigation
Reform Act of 1995. These forward-looking statements can be identified by terminology such as “may,” “will,” “expect,”
“anticipate,” “aim,” “estimate,” “intend,” “plan,” “believe,”
“potential,” “continue,” “is/are likely to” or other similar expressions. Such statements are based
upon current expectations and current market and operating conditions and relate to events that involve known or unknown risks, uncertainties
and other factors, all of which are difficult to predict and many of which are beyond the Company’s or Board’s control, which
may cause actual results, performance or achievements to differ materially from those in the forward-looking statements. Further information
regarding these and other risks, uncertainties or factors is included in the Company’s filings with the U.S. Securities and Exchange
Commission. The Company and Board do not undertake any obligation to update any forward-looking statement as a result of new information,
future events or otherwise, except as required under law.
Contact
Sinovac
Biotech Ltd.
Helen
Yang
Tel:
+86-10-8279 9720
Email:
ir@sinovac.com
SINOVAC BIOTECH LTD.
Consolidated Balance Sheets
As of December 31, 2025 and 2024
(Expressed
in thousands of U.S. Dollars)
| | |
December 31,
2025 | | |
December 31,
2024 | |
| | |
(Audited) | | |
(Audited) | |
| ASSETS | |
| | |
| |
| Current assets | |
| | |
| |
| Cash and cash equivalents | |
$ | 488,248 | | |
$ | 335,273 | |
| Restricted cash | |
| 668,181 | | |
| 266,944 | |
| Short-term investments | |
| 5,483,073 | | |
| 9,613,328 | |
| Accounts receivable, net | |
| 286,344 | | |
| 300,887 | |
| Inventories | |
| 94,309 | | |
| 96,920 | |
| Prepaid expenses and other current assets | |
| 17,600 | | |
| 15,721 | |
| Income tax receivable | |
| 4,225 | | |
| 4,011 | |
| Amounts due from related parties | |
| 22,518 | | |
| 11,431 | |
| Total current assets | |
| 7,064,498 | | |
| 10,644,515 | |
| Property, plant and equipment, net | |
| 706,059 | | |
| 880,968 | |
| Prepaid land use rights, net | |
| 62,172 | | |
| 61,525 | |
| Intangible assets, net | |
| 77,679 | | |
| 122,579 | |
| Long-term investments | |
| 512,324 | | |
| 491,349 | |
| Prepayments for acquisition of equipment | |
| 2,138 | | |
| 1,340 | |
| Deferred tax assets | |
| 41,520 | | |
| 37,373 | |
| Operating lease right-of-use assets | |
| 10,435 | | |
| 16,024 | |
| Other non-current assets | |
| 18,282 | | |
| 20,488 | |
| Goodwill | |
| 12,604 | | |
| 27,508 | |
| Amounts due from related parties | |
| 34,014 | | |
| 33,612 | |
| Total non-current assets | |
| 1,477,227 | | |
| 1,692,766 | |
| Total assets | |
$ | 8,541,725 | | |
$ | 12,337,281 | |
| LIABILITIES AND EQUITY | |
| | | |
| | |
| Current liabilities | |
| | | |
| | |
| Short-term bank loans and current portion of long-term bank loans | |
$ | 229,374 | | |
$ | 211,919 | |
| Accounts payable and accrued liabilities | |
| 604,676 | | |
| 802,996 | |
| Income tax payable | |
| 30,687 | | |
| 207,718 | |
| Deferred revenue | |
| 11,265 | | |
| 12,211 | |
| Deferred government grants, current | |
| 3,035 | | |
| 1,728 | |
| Dividend payable | |
| 657,856 | | |
| 212,960 | |
| Operating lease liabilities, current | |
| 2,118 | | |
| 2,366 | |
| Amounts due to related parties | |
| 1,354 | | |
| — | |
| Total current liabilities | |
| 1,540,365 | | |
| 1,451,898 | |
| Deferred government grants, non-current | |
| 5,892 | | |
| 4,843 | |
| Long-term bank loans | |
| 265,484 | | |
| 163,840 | |
| Deferred tax liabilities | |
| 325,068 | | |
| 410,049 | |
| Operating lease liabilities, non-current | |
| 8,640 | | |
| 13,198 | |
| Other non-current liabilities | |
| 24 | | |
| 23 | |
| Total long-term liabilities | |
| 605,108 | | |
| 591,953 | |
| Total liabilities | |
$ | 2,145,473 | | |
$ | 2,043,851 | |
| Equity | |
| | | |
| | |
| Common stock | |
$ | 72 | | |
$ | 72 | |
| Additional paid-in capital | |
| 550,168 | | |
| 550,168 | |
| Accumulated other comprehensive loss | |
| (513,252 | ) | |
| (707,806 | ) |
| Statutory surplus reserves | |
| 1,586,013 | | |
| 1,581,467 | |
| Retained earnings | |
| 2,815,942 | | |
| 6,838,357 | |
| Total Sinovac shareholders’ equity | |
| 4,438,943 | | |
| 8,262,258 | |
| Non-controlling interests | |
| 1,957,309 | | |
| 2,031,172 | |
| Total equity | |
| 6,396,252 | | |
| 10,293,430 | |
| Total liabilities and equity | |
$ | 8,541,725 | | |
$ | 12,337,281 | |
SINOVAC BIOTECH LTD.
Consolidated Statements of Operations and Comprehensive Income (Loss)
For
the six months and year ended December 31, 2025 and 2024
(Expressed in thousands of U.S. Dollars, except for numbers of shares and per share data)
| | |
Six months ended December 31, | | |
Year ended December 31, | |
| | |
2025 | | |
2024 | | |
2025 | | |
2024 | |
| | |
(Unaudited
and
Unreviewed) | | |
(Unaudited
and
Unreviewed) | | |
(Audited) | | |
(Audited) | |
| Sales | |
$ | 255,743 | | |
$ | 232,663 | | |
$ | 386,013 | | |
$ | 361,374 | |
| Cost of sales | |
| 75,224 | | |
| 81,537 | | |
| 124,032 | | |
| 140,688 | |
| Gross profit | |
| 180,519 | | |
| 151,126 | | |
| 261,981 | | |
| 220,686 | |
| Selling, general and administrative expenses | |
| 185,768 | | |
| 212,320 | | |
| 332,979 | | |
| 420,922 | |
| Provision for credit losses | |
| 4,953 | | |
| 8,257 | | |
| 4,144 | | |
| 12,306 | |
| Research and development expenses | |
| 89,254 | | |
| 128,330 | | |
| 216,180 | | |
| 270,661 | |
| Loss on disposal and impairment of property, plant and equipment | |
| 135,418 | | |
| 24,965 | | |
| 137,235 | | |
| 30,279 | |
| Loss on impairment of intangible assets | |
| (2,173 | ) | |
| — | | |
| 49,922 | | |
| — | |
| Loss on impairment of goodwill | |
| (351 | ) | |
| — | | |
| 15,686 | | |
| — | |
| Government grants recognized in income | |
| (491 | ) | |
| (6,903 | ) | |
| (4,035 | ) | |
| (7,947 | ) |
| Total operating expenses | |
| 412,378 | | |
| 366,969 | | |
| 752,111 | | |
| 726,221 | |
| Operating loss | |
| (231,859 | ) | |
| (215,843 | ) | |
| (490,130 | ) | |
| (505,535 | ) |
| Interest and financing expenses | |
| (5,723 | ) | |
| (3,462 | ) | |
| (9,819 | ) | |
| (5,637 | ) |
| Interest income | |
| 20,342 | | |
| 13,120 | | |
| 33,281 | | |
| 29,073 | |
| Share of earnings (losses) from equity method investments | |
| 4,204 | | |
| 6,038 | | |
| (4,036 | ) | |
| (2,700 | ) |
| Other income, net | |
| 46,708 | | |
| 233,032 | | |
| 208,602 | | |
| 527,636 | |
| (Loss) income before income taxes | |
| (166,328 | ) | |
| 32,885 | | |
| (262,102 | ) | |
| 42,837 | |
| Income tax benefit (expense) | |
| 64,047 | | |
| (51,180 | ) | |
| 63,266 | | |
| (2,181 | ) |
| Net (loss) income | |
| (102,281 | ) | |
| (18,295 | ) | |
| (198,836 | ) | |
| 40,656 | |
| Less: net loss attributable to non-controlling interests | |
| (64,267 | ) | |
| (15,346 | ) | |
| (139,156 | ) | |
| (50,249 | ) |
| Net (loss) income attributable to common shareholders of Sinovac | |
$ | (38,014 | ) | |
$ | (2,949 | ) | |
$ | (59,680 | ) | |
$ | 90,905 | |
| | |
| | | |
| | | |
| | | |
| | |
| Earnings (loss) per share | |
| | | |
| | | |
| | | |
| | |
| Basic net (loss) income per share | |
| (0.53 | ) | |
| (0.04 | ) | |
| (0.83 | ) | |
| 1.27 | |
| Diluted net (loss) income per share | |
| (0.53 | ) | |
| (0.04 | ) | |
| (0.83 | ) | |
| 1.27 | |
| Weighted average number of shares of common stock outstanding | |
| | | |
| | | |
| | | |
| | |
| – Basic | |
| 71,860,702 | | |
| 71,860,702 | | |
| 71,860,702 | | |
| 71,860,702 | |
| – Diluted | |
| 71,860,702 | | |
| 71,860,702 | | |
| 71,860,702 | | |
| 71,860,702 | |
| | |
| | | |
| | | |
| | | |
| | |
| Net (loss) income | |
$ | (102,281 | ) | |
$ | (18,295 | ) | |
$ | (198,836 | ) | |
$ | 40,656 | |
| Other comprehensive income (loss), net of tax of nil | |
| | | |
| | | |
| | | |
| | |
| Foreign currency translation adjustments | |
| 152,377 | | |
| (43,335 | ) | |
| 273,972 | | |
| (223,857 | ) |
| Unrealized gain (loss) on available-for-sale investments | |
| 3,185 | | |
| 3,176 | | |
| 6,729 | | |
| (10,619 | ) |
| Comprehensive income (loss) | |
| 53,281 | | |
| (58,454 | ) | |
| 81,865 | | |
| (193,820 | ) |
| Less: comprehensive loss attributable to non-controlling interests | |
| (15,561 | ) | |
| (29,153 | ) | |
| (53,009 | ) | |
| (140,337 | ) |
| Comprehensive income (loss) attributable to shareholders of Sinovac | |
$ | 68,842 | | |
$ | (29,301 | ) | |
$ | 134,874 | | |
$ | (53,483 | ) |
SINOVAC BIOTECH LTD.
Consolidated Statements of Cash Flows
For
the six months and year ended December 31, 2025 and 2024
(Expressed in thousands of U.S. Dollars)
| | |
Six months ended December 31, | | |
Year ended December 31, | |
| | |
2025 | | |
2024 | | |
2025 | | |
2024 | |
| | |
(Unaudited
and
Unreviewed) | | |
(Unaudited
and
Unreviewed) | | |
(Audited) | | |
(Audited) | |
| Operating activities | |
| | |
| | |
| | |
| |
| Net (loss) income | |
$ | (102,281 | ) | |
$ | (18,295 | ) | |
$ | (198,836 | ) | |
$ | 40,656 | |
| Adjustments to reconcile net (loss) income to net cash (used in) provided by operating activities: | |
| | | |
| | | |
| | | |
| | |
| - Deferred income taxes | |
| (75,489 | ) | |
| 6,577 | | |
| (89,911 | ) | |
| (56,406 | ) |
| - Inventory provision | |
| 13,422 | | |
| 9,723 | | |
| 30,595 | | |
| 37,112 | |
| - Provision for credit losses | |
| 4,953 | | |
| 8,257 | | |
| 4,144 | | |
| 12,306 | |
| - Loss on disposal and impairment of property, plant and equipment | |
| 135,418 | | |
| 24,965 | | |
| 137,235 | | |
| 30,279 | |
| - Loss on impairment of intangible assets | |
| (2,173 | ) | |
| — | | |
| 49,922 | | |
| — | |
| - Loss on impairment of goodwill | |
| (351 | ) | |
| — | | |
| 15,686 | | |
| — | |
| - Depreciation of property, plant and equipment | |
| 49,504 | | |
| 52,304 | | |
| 97,446 | | |
| 110,227 | |
| - Amortization of prepaid land use rights | |
| 1,144 | | |
| 1,134 | | |
| 2,261 | | |
| 2,257 | |
| - Amortization of intangible assets | |
| 709 | | |
| 551 | | |
| 1,331 | | |
| 1,052 | |
| - Non-cash operating lease expense | |
| 1,029 | | |
| 3,468 | | |
| 2,626 | | |
| 5,252 | |
| - Accretion of discounts on investments | |
| (120 | ) | |
| (8,996 | ) | |
| (3,935 | ) | |
| (14,070 | ) |
| - Share of (earnings) losses from equity method
investments, net of dividends received | |
| (1,524 | ) | |
| (6,038 | ) | |
| 6,716 | | |
| 2,700 | |
| - Investment and interest income | |
| (72,716 | ) | |
| 22,978 | | |
| (190,814 | ) | |
| (104,797 | ) |
| Changes in operating assets and liabilities: | |
| | | |
| | | |
| | | |
| | |
| - Accounts receivable | |
| (5,478 | ) | |
| 10,506 | | |
| 24,267 | | |
| 87,733 | |
| - Inventories | |
| 4,200 | | |
| 27,346 | | |
| (23,019 | ) | |
| (665 | ) |
| - Income tax receivable and payable | |
| (190,700 | ) | |
| 19,374 | | |
| (177,168 | ) | |
| 11,354 | |
| - Prepaid expenses and other current assets | |
| 24,654 | | |
| 43,138 | | |
| 2,100 | | |
| 7,961 | |
| - Deferred revenue | |
| (1,171 | ) | |
| 5,964 | | |
| (1,463 | ) | |
| (14,443 | ) |
| - Accounts payable and accrued liabilities and other current liabilities | |
| 19,399 | | |
| 77,005 | | |
| (195,397 | ) | |
| (210,888 | ) |
| - Deferred government grants | |
| 3,008 | | |
| 95 | | |
| 2,774 | | |
| (144 | ) |
| - Other non-current assets and liabilities | |
| (6,975 | ) | |
| (2,094 | ) | |
| (8,744 | ) | |
| (4,367 | ) |
| Net cash (used in) provided by operating activities | |
| (201,538 | ) | |
| 277,962 | | |
| (512,184 | ) | |
| (56,891 | ) |
| Investing activities | |
| | | |
| | | |
| | | |
| | |
| - Purchase of investments | |
| (2,798,160 | ) | |
| (2,883,857 | ) | |
| (6,218,953 | ) | |
| (4,865,159 | ) |
| - Proceeds from maturity and sales of investments | |
| 3,235,913 | | |
| 3,184,032 | | |
| 10,673,092 | | |
| 5,594,972 | |
| - Proceeds from disposal of equipment | |
| 409 | | |
| 19 | | |
| 409 | | |
| 160 | |
| - Proceeds from dissolution of subsidiary | |
| 181 | | |
| — | | |
| 181 | | |
| — | |
| - Repayments received on loans made to service vendors | |
| — | | |
| 497 | | |
| — | | |
| 4,655 | |
| - Loan to related parties | |
| — | | |
| (10,085 | ) | |
| — | | |
| (33,754 | ) |
| - Purchase of property, plant and equipment | |
| (22,383 | ) | |
| (47,901 | ) | |
| (48,917 | ) | |
| (95,960 | ) |
| - Prepaid land use rights | |
| (235 | ) | |
| — | | |
| (235 | ) | |
| — | |
| - Acquisition of intangible assets | |
| (203 | ) | |
| (1,627 | ) | |
| (203 | ) | |
| (1,627 | ) |
| - Purchase of equity method investments | |
| (1,738 | ) | |
| (45,127 | ) | |
| (4,755 | ) | |
| (46,733 | ) |
| - Distributions of equity method investees | |
| 1,699 | | |
| — | | |
| 1,699 | | |
| — | |
| - Acquisition of business, net of cash acquired | |
| (14,148 | ) | |
| (100,195 | ) | |
| (14,148 | ) | |
| (100,195 | ) |
| Net cash provided by investing activities | |
| 401,335 | | |
| 95,756 | | |
| 4,388,170 | | |
| 456,359 | |
| Financing activities | |
| | | |
| | | |
| | | |
| | |
| - Proceeds from bank loans | |
| 59,889 | | |
| 68,568 | | |
| 318,401 | | |
| 204,775 | |
| - Repayments of bank loans | |
| (24,571 | ) | |
| (7,575 | ) | |
| (218,763 | ) | |
| (81,728 | ) |
| - Cash paid for dividends | |
| (3,300,332 | ) | |
| (713,622 | ) | |
| (3,534,344 | ) | |
| (946,997 | ) |
| Net cash used in financing activities | |
| (3,265,014 | ) | |
| (652,629 | ) | |
| (3,434,706 | ) | |
| (823,950 | ) |
| Effect of exchange rate changes on cash and cash equivalents and restricted cash | |
| 64,134 | | |
| (77,995 | ) | |
| 112,932 | | |
| (102,423 | ) |
| (Decrease)
Increase in cash and cash equivalents and restricted cash | |
| (3,001,083 | ) | |
| (356,906 | ) | |
| 554,212 | | |
| (526,905 | ) |
| Cash and cash equivalents and restricted cash, beginning of year | |
| 4,157,512 | | |
| 959,123 | | |
| 602,217 | | |
| 1,129,122 | |
| Cash and cash equivalents and restricted cash, end of year | |
$ | 1,156,429 | | |
$ | 602,217 | | |
$ | 1,156,429 | | |
$ | 602,217 | |
