FORM 6-K. SECURITIES AND EXCHANGE COMMISSION Washington D.C

Similar documents
Sinovac Biotech Co Ltd. 29 Nov- 1Dec 2010 GENEVA

Memory Pharmaceuticals Establishes Plans for Clinical Program for MEM 3454 in Schizophrenia. -Broadens Roche Nicotinic Alpha-7 Alliance-

VICAL INC FORM 8-K. (Current report filing) Filed 11/02/06 for the Period Ending 11/02/06

FORM8-K HILLENBRAND,INC.

DCP MIDSTREAM, LP FORM 8-K. (Current report filing) Filed 04/13/12 for the Period Ending 04/09/12

WALGREEN CO. FORM 8-K (Unscheduled Material Events) Filed 6/5/2006 For Period Ending 6/5/2006

Inovio Pharmaceuticals, Inc. (Exact name of registrant as specified in its charter)

PIERIS PHARMACEUTICALS, INC. (Exact Name of Registrant as Specified in its Charter)

VistaGen Therapeutics, Inc. (Exact name of registrant as specified in its charter)

Broad and clinically important benefits beyond the initial registrational endpoints are now reported.

Zogenix Announces Positive Top-line Results from Pivotal Phase 3 Clinical Trial of ZX008 in Dravet Syndrome

HILLENBRAND INDUSTRIES INC

VolitionRx Announces First Quarter 2016 Financial Results and Business Update

UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C Form 6-K

Feasibility of Production of Human AI Vaccine in AI vaccine Manufacturers in China. Gu Hong Ministry of Agriculture of P. R. China

USPSTF Draft Recommendations Investor Call. October 6, 2015

34 th Annual J.P. Morgan Healthcare Conference

Stainless-steel vs Single-use: The Vaccines Perspective

About X-Linked Hypophosphatemia (XLH)

Development of Recombinant MERS-CoV Spike (S) Nanoparticle Vaccine

Acasti Pharma Provides Business Update for the Third Quarter of Fiscal 2019

Cloudbreak. January Cidara Therapeutics

Results Confirm and Extend 40-Week Findings that Treatment with Crysvita is Superior to Conventional Therapy

Oragenics Shareholder Update

RULES OF CONDUCT OF INSIDERS RESPECTING

Intercell and Novartis form world leading strategic partnership to drive vaccines innovation

Merck Announces FDA Approval of KEYTRUDA. Provided to Investors as a Reference

Evofem Biosciences Reports Second Quarter 2018 Financial Results and Provides Corporate Update

Theravance Announces Positive Results from Phase 1 and Phase 2 Clinical Studies with TD-1211 in Development for Opioid-Induced Constipation

Cloudbreak. March Cidara Therapeutics

FORM8-K HILLENBRAND,INC.

Aviragen Therapeutics, Inc. and Vaxart Inc. Joint Conference Call UNLOCKING THE FULL POTENTIAL OF ORAL VACCINES

UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C FORM 8-K

Valneva Reports Strong 2017 Revenues Driven by Double Digit Product Sales Growth

VIA ELECTRONIC MAIL. September 15, Barbara Z Sweeney Office of the Corporate Secretary NASD 1735 K Street, NW Washington, DC

Synergy Pharmaceuticals TRULANCE (Plecanatide) Receives U.S. FDA Approval for the Treatment of Adults with Chronic Idiopathic Constipation

Acquisition of Novartis Influenza Vaccines Business. 27 th October 2014

Update on Exact Sciences Molecular CRC Screening Test. November 16 th, 2011

January 30, 2018 Dow Wilson President and Chief Executive Officer

Avenue Therapeutics, Inc. May 2017

Conventional therapy n=32. RGI-C Score (Primary Endpoint) LS Mean* (0.83, 1.45) P< Substantial healing, % patients (RGI-C +2.

Pandemic Influenza: Appropriations for Public Health Preparedness and Response

Avenue Therapeutics, Inc. August 2016

Pandemic Influenza: Appropriations for Public Health Preparedness and Response

PRESS RELEASE. Libourne, May 29 th, 2013: The signature of a scientific collaboration protocol about avian influenza vaccines between

Argos Therapeutics Reports Fourth Quarter and Year-End 2013 Financial Results

Capital Senior Living Corporation

-- Edasalonexent Substantially Slowed Duchenne Muscular Dystrophy Disease Progression through 36 Weeks --

Avenue Therapeutics, Inc. September 2016

Corporate Presentation

Developing & Commercializing Targeted Small Molecule Drugs in Cancer

M (SAPPHIRE-II)

ADAPTIMMUNE INVESTOR PRESENTATION. August 2016

Applicable Sectors: Public Health, Emergency Services.

Merck Pipeline. April 30, 2010

CytoDyn Announces Initiation of Metastatic Triple Negative Breast Cancer Trial and Reiterates Phase 3 Goal in Cancer

Syndax Announces Updated Results from Phase 2 ENCORE 601 Trial of Entinostat in Combination with KEYTRUDA (pembrolizumab)

-- Single Global Phase 3 Trial Expected to Begin in First Half of

ONO PHARMACEUTICAL CO., LTD. and Bristol-Myers Squibb Announce Strategic Immuno-Oncology Collaboration in Japan, South Korea and Taiwan

Oragenics, Inc. (Exact name of registrant as specified in its charter)

Pandemic Influenza Cross Sectoral Preparedness and Planning

TSX Venture: RVV OTCQB: RVVTF

WALGREENS BOOTS ALLIANCE, INC.

CAN-FITE BIOPHARMA LTD. (Exact name of Registrant as specified in its charter)

8 of 21 (38.1%) Achieved RECIST v1.1 Durable Complete Response (CR) in Predicted Anti-PD-1 Non-Responder Melanoma Patients at 24 Weeks

China Vaccine Market Report,

AVEO and Astellas Report Final Overall Survival Results from TIVO-1

More cancer patients are being treated with immunotherapy, but

ObsEva Reports Third Quarter 2017 Financial Results and Provides Business Update

Partnership Contribution Standard Operating Procedures June 2015


Walgreen Co. Reports Second Quarter 2010 Earnings Per Diluted Share of 68 Cents; Results Include 2 Cents Per Diluted Share of Restructuring Costs

AVEO and Astellas Announce Positive Findings from TIVO-1 Superiority Study of Tivozanib in First-Line Advanced RCC

PROMISE 1 Top-Line Data Results. June 27, 2017

AVEO and Astellas Announce TAURUS Patient Preference Clinical Study Comparing Tivozanib with Sunitinib in First-Line Kidney Cancer

Tamsulosin Hydrochloride 0.4 mg Capsule

When the question is genetics, the answer is Invitae Invitae Corporation. All Rights Reserved. 1

University of Colorado Denver. Pandemic Preparedness and Response Plan. April 30, 2009

Savient's Pegloticase Data in Treatment-Failure Gout Patients Presented at 72nd Annual Meeting of the American College of Rheumatology Conference

China Human Vaccine Industry Report, Mar. 2015

Preparing For Pandemic Influenza: What the CDC and HHS Recommend You Can Do

Edasalonexent (CAT-1004) Program

Verona Pharma Announces Positive Top-Line Data from Phase 2a Clinical Trial in COPD with RPL554 Dosed in Addition to Tiotropium (Spiriva )

Actinium Pharmaceuticals Highlights Analysis of Pivotal Iomab-B Phase 3 SIERRA Trial Presented in Oral Session at ASH Annual Meeting

WARNING: RISK OF SERIOUS DEHYDRATION IN PEDIATRIC PATIENTS

Capricor Therapeutics

Acorda Acquisition of Civitas Therapeutics. September 24, 2014

Beyond vaccine introduction: Working together for sustainable, resilient immunization programs Manufacturer perspective

UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C FORM 8-K

ARISTOTLE Demonstrated that ELIQUIS is the First Oral Anticoagulant to Significantly Reduce All-Cause Death

ObsEva Reports Third Quarter 2018 Financial Results and Provides Business Update

Bio-Path Announces Clinical Update to Interim Analysis of Phase 2 Prexigebersen Trial in Acute Myeloid Leukemia

China Human Vaccine Industry Report, May 2012

China Human Vaccine Industry Report, Jun. 2016

An Affordable Pandemic Influenza Vaccine Solution for Developing Countries (and Developed Countries Too)

(direct) (609) (mobile)

ARDELYX REPORTS POSITIVE T3MPO-2 PHASE 3 TRIAL RESULTS IN IBS-C

PANDEMIC INFLUENZA RESPONSE PLAN

China Human Vaccine Industry Report, Aug. 2013

Credit Suisse 27 th Annual Healthcare Conference

Transcription:

FORM 6-K SECURITIES AND EXCHANGE COMMISSION Washington D.C. 20549 REPORT OF FOREIGN ISSUER PURSUANT TO RULE 13a-16 OR 15d-16 OF THE SECURITIES EXCHANGE ACT OF 1934 For the month of April, 2009 Commission File Number: 001-32371 SINOVAC BIOTECH LTD. 39 Shangdi Xi Road Haidian District Beijing 100085, People s Republic of China (Address of principal executive offices) Indicate by check mark whether the registrant files or will file annual reports under cover Form 20-F or Form 40-F. Form 20-F X Form 40-F Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b) (1): Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b) (7): Indicate by check mark whether by furnishing the information contained in this Form, the registrant is also thereby furnishing the information to the Commission pursuant to Rule 12g3-2(b) under the Securities Exchange Act of 1934. Yes No X If "Yes" is marked, indicate below the file number assigned to the registrant in connection with Rule 12g3-2(b): 82- N/A

SINOVAC BIOTECH LTD. Form 6-K TABLE OF CONTENTS Signature 3 Exhibit 99.1 Press Release 4 Page

SIGNATURE 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. SINOVAC BIOTECH LTD. By: /s/ Weidong Yin Name: Weidong Yin Title: Chief Executive Officer, President Date: April 29, 2009

Exhibit 99.1 Sinovac Initiates Preparatory Activities for Swine Flu Vaccine On Thursday April 30, 2009, 11:58 am EDT BEIJING, April 30 /PRNewswire-FirstCall/ -- Sinovac Biotech Ltd. (NYSE Amex: SVA), a leading developer and provider of vaccines in China, today announced that the Company has initiated preparatory activities for the development of a vaccine for the new influenza A (H1N1) strain, Swine Flu, which is currently spreading throughout Mexico and other parts of the world. Sinovac has contacted various Chinese government authorities and other global health organizations in order to closely monitor the disease and evaluate strategies to control and prevent its transmission. Based on confirmation from health authorities, Sinovac expects to receive the swine flu virus strain in the near future, enabling the Company to commence manufacturing of the vaccine. Production will occur at the Company's vaccine manufacturing and filling and packaging facilities, which have Good Manufacturing Practice (GMP) certification from China's State Food and Drug Administration (SFDA). In 2008, following the receipt of a Chinese government grant, Sinovac expanded its annual manufacturing capacity for its pandemic influenza vaccine, Panflu(TM), to 20 million doses; these facilities can also be leveraged in the development of a Swine Flu vaccine. In April 2008, Sinovac received SFDA approval to produce Panflu. The approval of Panflu in China followed a fast track regulatory approval process, which enables a timely approval and rapid response to control the spread of new viruses before they can cause a human influenza pandemic. Panflu is an approved whole viron pandemic influenza vaccine for adults, however, the new flu virus has infected many children this time. In order to help prevent transmission of the disease among children, Sinovac has sped up the regulatory application process for its split pandemic influenza vaccine, which was developed for the pediatric population and the Company expects to provide both a whole viron vaccine and split vaccine to tackle the disease transmission. Mr. Weidong Yin, Chairman, President and CEO, commented, "As China's only approved manufacturer of a pandemic influenza (H5N1) vaccine, we have a fully integrated human vaccine development expertise and manufacturing capability to produce a Swine Flu vaccine following the receipt of the H1N1 strain. Our cumulative development efforts for Panflu have uniquely positioned Sinovac to rapidly develop a human Swine Flu vaccine prototype specific to the H1N1 virus strain. Once this vaccine strain is available from the global health authorities, we will be ready to produce vaccine as needed." About Sinovac Sinovac Biotech Ltd. is a China-based biopharmaceutical company that focuses on the research, development, manufacture and commercialization of vaccines that protect against human infectious diseases. Sinovac's vaccine products include Healive (hepatitis A), Bilive (combined hepatitis A and B), and Anflu (influenza). Panflu(TM), Sinovac's pandemic influenza vaccine (H5N1), has already been approved for government stockpiling.

Sinovac is developing vaccines for Enterovirus 71, Universal Pandemic Influenza, Japanese encephalitis vaccine, and Human Rabies vaccine. Its wholly-owned subsidiary, Tangshan Yian, is conducting field trials for independently developed inactivated animal rabies vaccines. 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. For more information, please contact: Helen G. Yang Sinovac Biotech Ltd. Tel: +86-10-8289-0088 x9871 Fax: +86-10-6296-6910 Email: info@sinovac.com Investors: Amy Glynn/Sara Ephraim The Ruth Group Tel: +1-646-536-7023/7002 Email: aglynn@theruthgroup.com sephraim@theruthgroup.com Media: Janine McCargo The Ruth Group Tel: +1-656-536-7033 Email: jmccargo@theruthgroup.com