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David  
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 More options Nov 5, 5:50 pm
From: David <david.dodd...@gmail.com>
Date: Thu, 5 Nov 2009 14:50:44 -0800 (PST)
Local: Thurs, Nov 5 2009 5:50 pm
Subject: News
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wittle  
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 More options Nov 5, 6:58 pm
From: wittle <jinsant...@gmail.com>
Date: Thu, 5 Nov 2009 15:58:57 -0800 (PST)
Local: Thurs, Nov 5 2009 6:58 pm
Subject: Re: News
So if Hong Kong is paying $10 a dose for 3 million doses and Sinovac
is supplying 65 million doses of h1n1 vaccine to the Chinese Gov.,
with tax credits, that equals 65 million x $10 and an unbelievable 650
million dollars. Their previous revenue guidance was revised up from
60 million dollars to an "unknown" figure. The 60 million was
previously revised up from 22 million. On Q2 SVA's return on equity
was 17.7%. Reuters has projected an EPS of .07 cents for Q3. Q2's EPS
was .14. Is my belief an EPS of .49 for Q3 realistic? If someone comes
up with a more exact EPS guess, I'd like to see it. The unknown is how
many doses of h1n1 will SVA receive payment for in this quarter. I
believe a partial order payment was paid by the Chinese Gov. for the
65 million doses ordered and the remaining (70%?) will be paid upon
delivery. So a ballpark guess is 50% of the revenue on 65 million
doses will be reported this quarter.

On Nov 5, 3:50 pm, David <david.dodd...@gmail.com> wrote:


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tickerwatch  
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 More options Nov 5, 7:32 pm
From: tickerwatch <aileenn...@gmail.com>
Date: Thu, 5 Nov 2009 16:32:18 -0800 (PST)
Local: Thurs, Nov 5 2009 7:32 pm
Subject: Re: News
The Chinese govt is paying around $3 per shot, and the calculation
should be based on doses already delivered(not 65 million). I wonder
if SVA is going to take the hit for the development cost of the drug
upfront or accrue it till year-end.  That would certain have an impact
on the profitability for the quarter.

On Nov 6, 7:58 am, wittle <jinsant...@gmail.com> wrote:


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oh buck market  
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 More options Nov 5, 7:47 pm
From: oh buck market <yhst...@gmail.com>
Date: Thu, 5 Nov 2009 16:47:51 -0800 (PST)
Local: Thurs, Nov 5 2009 7:47 pm
Subject: Re: News
So far, nobody knows how much the Chinese Government will pay for the
vaccine, however, since it is prohibited to be exported by Government,
and if China government just wants to pay only half of the
international market price, that means that shareholder's interest in
SVA is sacrificed, if it is so, can shareholders in USA sue SVA or
China government?

On Nov 5, 7:32 pm, tickerwatch <aileenn...@gmail.com> wrote:


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wittle  
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 More options Nov 5, 7:58 pm
From: wittle <jinsant...@gmail.com>
Date: Thu, 5 Nov 2009 16:58:22 -0800 (PST)
Local: Thurs, Nov 5 2009 7:58 pm
Subject: Re: News
There has to be some added incentives, tax credits, low interest
loans, additional payment for development cost, given to SVA by the
government. I've heard this $3 number, the price of two tootsie rolls.
I don't believe that number will be validated in the end. Just making
and moving the empty vials would cost $3 and the Chinese  gov. would
never force a company to run in the red. No, SVA will probably be
rewarded with free land and a new facility, besides a bunch of medals,
for their heroic efforts.

On Nov 5, 5:32 pm, tickerwatch <aileenn...@gmail.com> wrote:


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sakalas91  
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 More options Nov 5, 8:11 pm
From: sakalas91 <boris.baku...@gmail.com>
Date: Thu, 5 Nov 2009 17:11:31 -0800 (PST)
Local: Thurs, Nov 5 2009 8:11 pm
Subject: Re: News
For those wondering about Sinovac's future plans, here's an
interesting article from BIZCHINA

BIZCHINA> Top Biz News

Sinovac Biotech to transfer quote to NASDAQ from Amex

By Ding Qingfen (China Daily)
Updated: 2009-11-05 08:44

Sinovac Biotech Ltd, China's first officially approved H1N1 flu
vaccine maker, announced yesterday it would transfer its stock
exchange listing to the NASDAQ Global Market from NYSE Amex in a bid
to raise more funds and become a leading vaccine producer.

The spread of H1N1 flu in China has benefited Sinovac, which is
China's second largest H1N1 flu vaccine producer in volume terms. Its
shares are expected to start trading on the NASDAQ by mid-November.

The funds raised will be injected into expanding vaccine production
capacity, strengthening research capability and conducting mergers and
acquisitions, said corporate executives.

"Sinovac expects to be a leading international vaccine producer
through quality and reasonably-priced products to Chinese and others
in need," said Yin Weidong, chairman of Sinovac Biotech Ltd.

Sinovac has an annual H1N1 vaccine output to meet the needs of 30
million people, and it will expand the capacity for both flu and other
diseases, Yin said.

Besides, Sinovac will also increase research and development spending
from the current 5 to 10 percent, he said.

The company has started developing a vaccine for hand, foot and mouth
disease, the first to do so in China, and is expected to apply for
clinical trials next year.

Sinovac Biotech got listed on the NYSE Amex late in 2004, and had
planned for the transfer for long, but could not meet the market
requirements by NASDAQ due to its low share price, said Helen G Yang,
manager of the international business department at Sinovac Biotech.

When its shares started surging since early this year after the
outbreak of the H1N1 influenza, the company began to communicate with
the NASDAQ bourse in August, she said.

Since it started developing the H1N1 vaccine in early June, Sinovac's
share price has more than tripled during the past five months, from
around $2. On Tuesday, its stock closed at $7.91.

Compared with their share prices three months ago, the Hualan
Biological Engineering and Tiantan Biological shares had risen by 200
and 150 percent, respectively, at the end of October.

During the roadshow in late September, Sinovac was warmly welcomed by
the NASDAQ market. "I felt so surprised to see the strong recognition
of a Chinese vaccine producer," said Yin.

"The H1N1 flu and Sinovac's good performance during the outbreak have
increased the speed of its transfer to the NASDAQ."

Sinovac Biotech, established in 2001, was the first company in the
world to announce preliminary clinical trials of the vaccine and the
first to get approval for production from the Chinese government in
late August.

The company has won three orders for 11.49 million people, the second
largest supplier after Hualan Biological among the eight Chinese H1N1
flu vaccine producers.

As on Nov 1, the Chinese mainland had reported 47,500 H1N1 cases in 31
provinces and regions. It is estimated that 390 million Chinese need
to get vaccinated, but the nation had only ordered vaccines for 70
million people until October.

Sinovac said it expected to get more orders, and was speeding up
production, but "the benefits from the H1N1 flu vaccine are short-
term. What we are targeting is to become a leading vaccine producer
worldwide by leveraging our growing brand awareness," Yin said.

China is now the third largest vaccine market with a size of $1
billion annually.

On Nov 5, 6:58 pm, wittle <jinsant...@gmail.com> wrote:


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M.H.  
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 More options Nov 5, 8:20 pm
From: "M.H." <mnshers...@gmail.com>
Date: Thu, 5 Nov 2009 17:20:00 -0800 (PST)
Subject: Re: News
H5N1=http://www.proactiveinvestors.com.hk/sto..

On Nov 5, 8:11 pm, sakalas91 <boris.baku...@gmail.com> wrote:


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sakalas91  
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 More options Nov 5, 8:23 pm
From: sakalas91 <boris.baku...@gmail.com>
Date: Thu, 5 Nov 2009 17:23:31 -0800 (PST)
Local: Thurs, Nov 5 2009 8:23 pm
Subject: Re: News
I found this information with a link on Yahoo Finance"

From ClinicalTrials.gov
A Service of the U.S. National Institute of Health

A Clinical Trial With Influenza A/H1N1 Vaccines
This study has been completed.
First Received: August 10, 2009 Last Updated: October 28, 2009 History
of Changes
Sponsor: Sinovac Biotech Co., Ltd
Information provided by: Sinovac Biotech Co., Ltd
ClinicalTrials.gov Identifier: NCT00956111
Purpose

A single center, stratified, randomized and double-blind phase IV
clinical trial is to be conducted in healthy elders (equal to or more
than 61 years), adults (18-60 years), adolescents (12-17 years) and
children (3-11 years) to evaluate the safety and immunogenicity of
Sinovac's split-virion or whole-virion novel influenza A (H1N1)
vaccines.

Condition Intervention Phase
Influenza
Biological: split-virion, adjuvanted H1N1 vaccine of 7.5 μg per dose
Biological: split-virion, adjuvanted H1N1 vaccine of 15 μg per dose
Biological: split-virion, non-adjuvanted H1N1 vaccine of 15 μg per
dose
Biological: split-virion, non-adjuvanted H1N1 vaccine of 30 μg per
dose
Biological: whole-virion, adjuvanted H1N1 vaccine of 5 μg per dose
Biological: whole-virion, adjuvanted H1N1 vaccine of 10 μg per dose
Biological: placebo control
Phase IV

Study Type: Interventional
Study Design: Prevention, Randomized, Double Blind (Subject,
Caregiver, Investigator, Outcomes Assessor), Placebo Control, Parallel
Assignment, Safety/Efficacy Study
Official Title: A Double-blind, Randomized, Stratified and Controlled
Clinical Trial With Split-virion and Whole-virion, Adjuvanted and Non-
adjuvanted Influenza A/H1N1 Vaccines in Healthy Adults, Elders,
Adolescents and Children

http://clinicaltrials.gov/ct2/show/NCT00...

On Nov 5, 7:11 pm, sakalas91 <boris.baku...@gmail.com> wrote:


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sakalas91  
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 More options Nov 5, 9:18 pm
From: sakalas91 <boris.baku...@gmail.com>
Date: Thu, 5 Nov 2009 18:18:00 -0800 (PST)
Subject: Re: News
For some reason, the link does not lead to the study.  However, the
study can be accessed on clinicaltrials.gov by entering the following
number in the search box:  NCT00956111.  I'm not sure of the
ramifications of the information above.  Anybody know?

On Nov 5, 7:23 pm, sakalas91 <boris.baku...@gmail.com> wrote:


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bluepeter  
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 More options Nov 6, 5:35 am
From: bluepeter <davidsbluebe...@googlemail.com>
Date: Fri, 6 Nov 2009 02:35:40 -0800 (PST)
Local: Fri, Nov 6 2009 5:35 am
Subject: Re: News
The study you refer to is testing a new dual vaccine, combining both
seasonal and H1N1 flu, on different populations and in different doses
to verify its efficacy and obtain the clinical data to get 'dual'
vaccine approved for licence.

Great news for SVA.

An even STRONGER HOLD now ;-)
Hold on to your hat, things are nearing take off.

On 6 Nov, 02:18, sakalas91 <boris.baku...@gmail.com> wrote:


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sakalas91  
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 More options Nov 6, 7:31 am
From: sakalas91 <boris.baku...@gmail.com>
Date: Fri, 6 Nov 2009 04:31:38 -0800 (PST)
Local: Fri, Nov 6 2009 7:31 am
Subject: Re: News
Thanks bluepeter!  Am I right in assuming that Sinovac's listing on
ClinicalTrials.gov suggests it is trying to get approval from the FDA
to market its vaccine in the United States?

On Nov 6, 4:35 am, bluepeter <davidsbluebe...@googlemail.com> wrote:


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xb x  
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 More options Nov 6, 6:18 pm
From: xb x <stock....@gmail.com>
Date: Fri, 6 Nov 2009 15:18:36 -0800 (PST)
Local: Fri, Nov 6 2009 6:18 pm
Subject: News
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xb x  
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 More options Nov 6, 6:23 pm
From: xb x <stock....@gmail.com>
Date: Fri, 6 Nov 2009 15:23:24 -0800 (PST)
Local: Fri, Nov 6 2009 6:23 pm
Subject: News
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End of messages  

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