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2014-01-22

 

- Conference call scheduled for Thursday, May 22, 2014 at 8:00 AM EDT -
BEIJING, May 21, 2014 /PRNewswire/ -- Sinovac Biotech Ltd. (NASDAQ: SVA), a leading provider of biopharmaceutical products in China, announced today its unaudited first quarter financial results for the period ended March 31, 2014.
First Quarter 2014 Financial Highlights (period-over-period comparisons to first quarter 2013)
·   Quarterly sales increased by 34.8% to .5 million from .1 million.
·   Gross profit increased by 45.4% to .3 million from .1 million. Gross margin was 75.8%, compared to 70.2%.
·   Net income attributable to common stockholders was ,000, or {value}.00 per basic and diluted share, compared to a net loss attributable to common stockholders of .0 million, or {value}.04 per basic and diluted share.
·   Cash and cash equivalents totaled 1.7 million as of March 31, 2014, compared to 7.2 million as of December 31, 2013.
Recent Business Highlights
Sinovac was awarded a government grant of RMB 60 million for the construction of a dedicated production facility for its enterovirus 71 (EV71) vaccine against hand foot and mouth disease (HFMD). This grant, which was approved by China's Ministry of Finance, National Development and Reform Commission, Ministry of Industry and Information Technology, and National Health and Family Planning Commission, will be funded in several tranches, of which RMB 20 million is expected in 2014, with the balance to be provided after certain criteria are met.
On May 21, 2014, Sinovac received approval from the China Food and Drug Administration (or "CFDA") to commence a human clinical trial of its 23-valent Pneumococcal polysaccharides vaccine (PPV). The trial is expected to begin in late 2014.  
Sinovac entered into a license agreement with Intravacc (Institute for Translational Vaccinology) in The Netherlands to develop and commercialize the Sabin Inactivated Polio Vaccine (sIPV) for China and other countries.
Sinovac was awarded a public tender in Mongolia to supply approximately 147,000 doses of inactivated hepatitis A vaccine to the Mongolian government for its 2014 national vaccination program. The hepatitis A vaccine was delivered in two batches in February and April.
Sinovac was selected by the Gansu Province Center for Disease Control (or Gansu CDC) as the sole supplier of 40,000 doses of inactivated hepatitis A vaccine for its emergency stockpiling program for 2014.This order will be supplied in full in 2014, with the timing of shipments to be directed by the Gansu CDC.                         
Sinovac obtained a registration license for Healive, its inactivated hepatitis A vaccine, from Instituto de Salud Publica de Chile, Chile's Institute of Public Health. The license is valid for five years from the date of issuance.
Mr. Weidong Yin, Chairman, President and CEO, commented, "The 34.8% year-over-year top line increase marked a strong first quarter. The growth was driven by higher sales of our commercialized vaccines in China, especially from Bilive, our combined hepatitis A&B vaccine. Sinovac's sales team continued to execute its tailored sales and marketing strategy, and maximize the favorable competitive environment."
Mr. Yin continued, "In line with our mission to develop and commercialize vaccines that address unmet medical needs in China and other countries, we continue to advance our pipeline vaccine candidates and expand our portfolio. Obtaining regulatory approval to commence human trials of PPV is another milestone we achieved. Our clinical application for the varicella vaccines is under review by CFDA."
Mr. Yin concluded, "The technology transfer agreement with Intravacc for sIPV exemplifies Sinovac's strategy to expand its vaccine pipeline through external collaboration. As the administration of an inactivated polio vaccine will largely reduce the risk of paralysis associated with the live attenuated vaccine virus in OPV, Sinovac is at the forefront of bringing a safer and more affordable solution to the population worldwide. Under the World Health Organization's global polio eradication plan, sIPV has significant market potential for Sinovac both in China and international markets. We are poised to continue to expand our vaccine portfolio focused on the objective of providing high quality vaccines made in China to children around the world."
Financial Review for Unaudited First Quarter Ended March 31, 2014
An analysis of sales and gross profit is as follows:                                              

 
In USD'000
(Unaudited)
2014Q1
% of Sales
2013Q1
%of Sales
Hepatitis A – Healive
6,439
47.5%
6,165
61.3%
Hepatitis A&B – Bilive
5,999
44.3%
2,995
29.8%
Hepatitis vaccines
12,438
91.8%
9,160
91.1%
Influenza vaccines
61
0.4%
294
3.0%
Animal vaccines
25
0.2%
13
0.1%
Mumps vaccines
920
6.8%
585
5.8%
Regular sales
13,444
99.2%
10,052
100%
H5N1
102
0.8%
-
-
Total sales
13,546
100%
10,052
100%
Cost of goods sold
3,278
24.2%
2,992
29.8%
Gross profit
10,268
75.8%
7,060
70.2%

First quarter 2014 sales increased by 34.8% to .5 million, from .1 million for the same period in 2013. The growth in regular sales was mainly due to an increase of Bilive revenue from million to million.
Compared to the first quarter of 2013, gross profit margin for the first quarter of 2014 increased to 75.8% from 70.2%. The increase in gross margin was mainly driven by lower unit costs for Healive and Bilive due to higher plant utilization, allowing the Company to leverage economies of scale. Gross margin was also favorably impacted by a decrease in the sales return provision compared to the same period last year.
Selling, general and administrative expenses for the first quarter of 2014 were .8 million, compared to .1 million in the same period of 2013. Selling expenses as a percentage of first quarter 2014 regular sales were 27.9%, down slightly from 29.9% in the same period of 2013 as the Company generated more revenue without significantly increasing fixed selling expenses. G&A expenses in the first quarter of 2014 were .0 million compared to .1 million in the same period of 2013. First quarter 2014 G&A expenses included a {value}.5 million foreign exchange loss due to the appreciation of the US dollar against the RMB. Excluding this foreign exchange loss, G&A expenses in the first quarter of 2014 were .5 million. The decrease in G&A expense was primarily due to the fact that the Company's Changping facility commenced production, and related depreciation was recorded in production costs.
R&D expenses for the first quarter of 2014 were .7 million, consistent with .8 million in the same period in 2013. The Company's main focus in the first quarter of 2014 was the continued optimization of production process for its PPV and varicella vaccine.  
Net income attributable to common stockholders was ,000, or {value}.00 per basic and diluted share, compared to a net loss attributable to common stockholders of .0 million, or {value}.04 per basic and diluted share.
Cash and cash equivalents totaled 1.7 million as of March 31, 2014, compared to 7.2 million as of December 31, 2013. Net cash used in operating activities was .8 million during the first quarter 2014. Net cash used in investing activities during the first quarter of 2014 was .2 million, which was primarily for payment of property, plant and equipment for the Changping facility. Net cash provided by financing activities during the first quarter of 2014 was .4 million, including loan proceeds of .3 million. 

Conference Call Details
The Company will host a conference call on Thursday, May 22, 2014 at 8:00 a.m. EDT (May 22, 2014 at 8:00 p.m. China Standard Time) to review the Company's financial results and provide an update on recent corporate developments. To access the conference call, please dial 1-877-407-0784 (USA) or 1-201-689-8560 (International). A replay of the call will be available from 11 a.m. EDT on May 22, 2014 to June 5, 2014 at midnight. To access the replay, please dial 1-877-870-5176 (USA) or 1-858-384-5517 (International) and reference the replay pin number 13582662.
A live audio webcast of the call will also be available from the investors section on the corporate web site at www.sinovac.com. A webcast replay can be accessed on the corporate website beginning May 22, 2014 and the replay will remain available for 30 days.

About Sinovac
Sinovac Biotech Ltd. is a China-based biopharmaceutical company that focuses on the research, development, manufacturing and commercialization of vaccines that protect against human infectious diseases including hepatitis A and B, seasonal influenza, H5N1 pandemic influenza (avian flu), H1N1 influenza (swine flu) and mumps, as well as animal rabies vaccine for canines. The Company filed a new drug application for enterovirus 71 (against hand, foot and mouth disease) with China Food & Drug Administration. In 2009, Sinovac was the first company worldwide to receive approval for its H1N1 influenza vaccine, Panflu.1, and has manufactured it for the Chinese Central Government, pursuant to the government-stockpiling program. The Company is also the only supplier of the H5N1 pandemic influenza vaccine to the government-stockpiling program. Sinovac is developing a number of new pipeline vaccines including vaccines for pneumococcal polysaccharides, pneumococcal conjugate, varicella and sIPV. Sinovac sells its vaccines mainly in China and exports selected vaccines to Mongolia, Nepal, and the Philippines. Sinovac has also been granted a license to commercialize seasonal flu vaccine in Mexico and hepatitis A vaccine in Chile.

Safe Harbor Statement
This announcement contains forward-looking statements. These statements are made under the "safe harbor" provisions of the U.S. Private Securities Litigation Reform Act of 1995. These forward-looking statements can be identified by words or phrases such as "will," "expects," "anticipates," "future," "intends," "plans," "believes," "estimates" and similar statements. Among other things, the business outlook and quotations from management in this press release contain forward-looking statements. Statements that are not historical facts, including statements about Sinovac's beliefs and expectations, are forward-looking statements. Forward-looking statements involve inherent risks and uncertainties. A number of important factors could cause actual results to differ materially from those contained in any forward-looking statement. Sinovac does not undertake any obligation to update any forward-looking statement, except as required under applicable law.
Helen Yang/Chris Lee 
Sinovac Biotech Ltd. 
Tel: +86-10-8279-9659/9696 
Fax: +86-10-6296-6910 
Email: ir@sinovac.com
Investors: 
Lee Roth 
The Ruth Group 
Tel: +1-646-536-7012 
Email: lroth@theruthgroup.com
Media: 
Aaron Estrada 
The Ruth Group 
Tel: +1-646-536-7028 
Email: aestrada@theruthgroup.com
 
 

SINOVAC BIOTECH LTD.
Consolidated Balance Sheets
As of December 31, 2013 and March 31,2014
(Expressed in thousands of U.S. Dollars, except for number of shares and per share data)
Mar 31, 2014
Dec 31, 2013
ASSETS
(Unaudited)
(Audited)
Current assets
Cash and cash equivalents
$
101,652
$
107,242
Accounts receivable
36,282
31,927
Inventories
15,653
14,329
Prepaid expenses and deposits
1,278
1,150
Deferred tax assets
2,037
2,602
Total current assets
156,902
157,250
Property, plant and equipment
65,143
67,963
Prepaid land lease payments
10,592
10,948
Long-term inventories
3,618
2,781
Long-term prepaid expenses
107
154
Prepayments for acquisition of equipment
1,108
708
Deferred tax assets
305
117
Licenses
652
772
Total   assets
$
238,427
$
240,693
LIABILITIES AND EQUITY
Current liabilities
Bank loans and current portion of long-term debt
$
32,844
$
16,217
Current portion of loan from a non-controlling shareholder
3,237
3,324
Accounts payable and accrued liabilities                                          
26,529
28,037
Income tax payable
239
246
Deferred revenue
183
875
Deferred government grants
448
458
Total current liabilities
63,480
49,157
Deferred government grants
4,507
4,746
Long-term debt
17,501
32,146
Deferred revenue
10,717
11,005
Total long term liabilities
32,725
47,897
Total liabilities
96,205
97,054
Commitments and contingencies
EQUITY
Common stock
56
56
Additional paid-in capital
107,619
107,393
Accumulated other comprehensive income
12,394
14,141
Statutory surplus reserves
11,808
11,808
Accumulated deficit
(4,710)
(4,714)
Total stockholders' equity
127,167
128,684
Non-controlling interests
15,055
14,955
Total equity
142,222
143,639
Total liabilities and equity
$
238,427
$
240,693

 
 
 

SINOVAC BIOTECH LTD.
 Consolidated Statements of Comprehensive Income (Loss)
 For the three months ended March 31, 2013 and 2014
 (Expressed in thousands U.S. Dollars, except for number of shares and per share data)
 Three Months Ended
Mar 31, 2014
Mar 31, 2013
(Unaudited)
(Unaudited)
 Sales
$
13,546
$
10,052
 Cost of sales
3,278
2,992
 Gross profit
10,268
7,060
 Selling, general and administrative expenses
7,792
7,136
 Provision for doubtful accounts
162
282
 Research and development expenses
1,702
1,848
 Loss (income) on disposal and Impairment of property, plant and
equipment
-
(2)
 Total operating expenses
9,656
9,264
 Operating income (loss)
612
(2,204)
 Interest and financing expenses 
(750)
(663)
 Interest income
780
441
 Other income (expenses)
146
61
 Income (loss) before income taxes and non-controlling interests 
788
(2,365)
 Income tax benefit (expense)
(347)
(2)
 Net income (loss)
441
(2,367)
 Less: (income) loss attributable to the non-controlling interests
(437)
358
 Net income (loss) attributable to stockholders of Sinovac                         
$
4
$
(2,009)
 Other comprehensive income (loss), net of tax of nil
 Foreign currency translation adjustments
(2,084)
234
 Total comprehensive income (loss)
(1,643)
(2,133)
 Less: comprehensive (income) loss attributable to non-controlling interests
(100)
329
 Comprehensive income (loss) attributable to stockholders
of Sinovac
$
(1,743)
$
(1,804)
 Basic and diluted earning (loss) per share
$
0.00
$
(0.04)
 Weighted average number of shares of common stock
outstanding
  Basic
55,587,029
55,097,228
  Diluted
56,110,870
55,097,228

 
 
 

SINOVAC BIOTECH LTD.
 Consolidated Statements of Cash Flows
 For the three months ended March 31, 2013 and 2014
 (Expressed in thousands U.S. Dollars)
Three months ended
Mar 31, 2014
Mar 31, 2013
(Unaudited)
(Unaudited)
Cash flows provided by (used in) operating activities
Net income (loss)
$
441
$
(2,365)
  Adjustments to reconcile net income (loss) to net cash
  provided by (used in) operating activities:
 - deferred income taxes
311
2
 - stock-based compensation
72
76
 - inventory provision
221
-
 - provision for doubtful accounts
162
282
 - impairment of equipment and loss on disposal
-
438
 - depreciation of property, plant and equipment and
   amortization of licenses
2,631
1,626
 - amortization of the prepaid land lease payments
67
72
 - accretion expenses
27
-
Changes in:
 - accounts receivable
(4,981)
(3,777)
 - inventories
(2,879)
(3,075)
 - income tax payable
7
-
 - prepaid expenses and deposits
(582)
(144)
 - deferred revenue
(718)
(1,067)
 - accounts payable and accrued liabilities
(577)
2,364
Net cash used in operating activities
(5,798)
(5,568)
Cash flows provided by financing activities
 - Loan proceeds
5,735
7,480
 - Loan repayments
(2,458)
-
 - Proceeds from issuance of common stock,
   net of share issuance costs
105
164
 - Proceeds from shares subscribed
49
11
 - Government grants received
-
304
Net cash provided by financing activities
3,431
7,959
Cash flows used in investing activities
 - Acquisition of property, plant and equipment
(2,204)
(2,160)
Net cash used in investing activities
(2,204)
(2,160)
Exchange gain (loss) on cash and cash equivalents
(1,019)
90
Increase (decrease) in cash and cash equivalents
(5,590)
321
Cash and cash equivalents, beginning of year
107,242
91,241
Cash and cash equivalents, end of year
$
101,652
$
91,562

 

Selling, general and administrative expenses for the first quarter of 2014 were .8 million, compared to .1 million in the same period of 2013. Selling expenses as a percentage of first quarter 2014 regular sales were 27.9%, down slightly from 29.9% in the same period of 2013 as the Company generated more revenue without significantly increasing fixed selling expenses. G&A expenses in the first quarter of 2014 were .0 million compared to .1 million in the same period of 2013. First quarter 2014 G&A expenses included a {value}.5 million foreign exchange loss due to the appreciation of the US dollar against the RMB. Excluding this foreign exchange loss, G&A expenses in the first quarter of 2014 were .5 million. The decrease in G&A expense was primarily due to the fact that the Company's Changping facility commenced production, and related depreciation was recorded in pr

oduction costs.

of the US dollar against the RMB. Excluding this foreign exchange loss, G&A expenses in the first quarter of 2014 were .5 million. The decrease in G&A expense was primarily due to the fact that the Company's Changping facility commenced production, and related depreciation was recorded in production costs.Selling, general and administrative expenses for the first quarter of 2014 were .8 million, compared to .1 million in the same period of 2013. Selling expenses as a percentage of first quarter 2014 regular sales were 27.9%, down slightly from 29.9% in the same period of 2013 as the Company generated more revenue without significantly increasing fixed selling expenses. G&A expenses in the first quarter of 2014 were .0 million compared to .1 million in the same period of 2013. First quarter 2014 G&A expenses included a {value}.5 million foreign exchange loss due to the appreciation

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About SINOVAC

 

Sinovac Biotech Ltd. (SINOVAC) is a China-based biopharmaceutical company that focuses on the R&D, manufacturing, and commercialization of vaccines that protect against human infectious diseases.

 

SINOVAC's product portfolio includes vaccines against COVID-19, enterovirus 71 (EV71) infected Hand-Foot-Mouth disease (HFMD), hepatitis A, varicella, influenza, poliomyelitis, pneumococcal disease, and mumps.

 

The COVID-19 vaccine, CoronaVac®, has been approved for use in more than 60 countries and regions worldwide. The hepatitis A vaccine, Healive®, passed WHO prequalification requirements in 2017. The EV71 vaccine, Inlive®, is an innovative vaccine under "Category 1 Preventative Biological Products" and was commercialized in China in 2016. In 2022, SINOVAC's Sabin-strain inactivated polio vaccine (sIPV) and varicella vaccine were prequalified by the WHO.

 

SINOVAC was the first company to be granted approval for its H1N1 influenza vaccine Panflu.1®, which has supplied the Chinese government's vaccination campaign and stockpiling program. The Company is also the only supplier of the H5N1 pandemic influenza vaccine, Panflu®, to the Chinese government stockpiling program.

 

SINOVAC continually dedicates itself to new vaccine R&D, with more combination vaccine products in its pipeline, and constantly explores global market opportunities. SINOVAC plans to conduct more extensive and in-depth trade and cooperation with additional countries, and business and industry organizations.

 

For more information, please see the Company’s website at www.sinovac.com.

 

Contact:

Sinovac Biotech Ltd. 

PR Team 

pr@sinovac.com