Wyeth Pharmaceuticals and Nautilus Biotech Announce Collaboration to Develop Hemophilia Therapies

Press Releases »

MADISON, N.J--5 Feb--PRNewswire-AsiaNet/InfoQuest


Wyeth - World's Fourth Largest Biopharmaceutical Company - Builds on Commitment to Innovation in Hemophilia

Wyeth Pharmaceuticals, a division of Wyeth (NYSE: WYE), and Nautilus Biotech in Evry, France, today announced the signing of a research collaboration and license agreement to discover and develop novel recombinant Factor IX proteins for the treatment of hemophilia B. These extended half-life proteins will be designed to enhance patient convenience as they will reduce

the number and frequency of treatments needed.

As part of the agreement, Nautilus Biotech will apply its proprietary technology to improve the duration of action of recombinant hemophilia B therapy. The Nautilus Biotech technology makes minimal and specific changes to amino acids sequences in order to slow the breakdown of the protein in the body.

"Wyeth is continually evaluating technologies for next-generation hemophilia products that provide unique and improved features for patients. This research partnership enhances Wyeth's presence in biopharmaceuticals and builds upon our history of innovation in hemophilia research," says Cavan Redmond, Executive Vice President and General Manager, BioPharma Business Unit

at Wyeth Pharmaceuticals.

Under the terms of this agreement, Wyeth will develop, manufacture and market products derived from the collaborative research. Nautilus Biotech will receive an upfront payment, research and development fees, milestone payments from Wyeth associated with development, regulatory filings and approvals, and royalty payments based on net sales of products.

"Wyeth has an impressive track record as a pioneer in developing state-of-the-art hemophilia therapies and Nautilus Biotech has a unique technology for improving protein medicines. We believe that the collaboration between Wyeth and Nautilus will offer exciting new therapeutic approaches for hemophilia," says Manuel Vega, Chief Executive Officer of Nautilus Biotech.

Hemophilia is a rare, inherited blood-clotting disorder that affects approximately 130,000 people worldwide. People with hemophilia are deficient in one of the key proteins -- either Factor VIII (hemophilia A) or Factor IX (hemophilia B) -- that are vital in the clotting cascade to prevent bleeding. Both forms of hemophilia are characterized by spontaneous hemorrhages or prolonged bleeding, typically into joints and soft tissue. Patients with hemophilia A or hemophilia B are dependent on protein replacement therapy with Factor VIII or Factor IX, respectively, for life.

Wyeth Pharmaceuticals, a division of Wyeth, has leading products in the areas of women's health care, cardiovascular disease, central nervous system, inflammation, transplantation, hemophilia, oncology, vaccines and nutritional products. Wyeth is one of the world's largest research-driven pharmaceutical and health care products companies. It is a leader in the discovery, development, manufacturing and marketing of pharmaceuticals, vaccines, biotechnology products and non-prescription medicines that improve the quality of life for people worldwide. The Company's major divisions include Wyeth Pharmaceuticals, Wyeth Consumer Healthcare and Fort Dodge Animal Health.

The statements in this press release that are not historical facts are forward-looking statements based on current xpectations of future events and are subject to risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. These risks and uncertainties include risks associated with the inherent uncertainty of the timing and success of product research, development and commercialization (including with respect to our pipeline products), drug pricing and payment for our products by government and third-party payors, manufacturing, data generated on the safety and efficacy of our products, economic conditions including interest and currency exchange rate fluctuations, changes in generally accepted accounting principles, the impact of competitive or generic products, trade buying patterns, global business operations, product liability and other types of litigation, the impact of legislation and regulatory compliance, intellectual property rights, strategic relationships with third parties, environmental liabilities, and other risks and uncertainties, including those detailed from time to time in our periodic

reports filed with the Securities and Exchange Commission, including our current reports on Form 8-K, quarterly reports on Form 10-Q and annual report on Form 10-K, particularly the discussion under the caption "ITEM 1A, RISK FACTORS." We assume no obligation to publicly update any forward-looking statements, whether as a result of new information, future developments or otherwise.

SOURCE Wyeth Pharmaceuticals

CONTACT: Media: Gerald Burr,

+1-484-865-5138, or

Candace Steele,

+1-484-865-5428,

both of Wyeth Pharmaceuticals;

Investor: Justin Victoria, of Wyeth,

+1-973-660-5340

Web site: http://www.wyeth.com

--Distributed by AsiaNet ( www.asianetnews.net )--


ข่าวWyeth Pharmaceuticals+Hemophiliaวันนี้

ไวเอท เปิดตัวพันธมิตรใหม่ในโครงการ Twinning Program ขององค์การฮีโมฟีเลียโลก

ไวเอทและชุมชนร่วมสานต่อปณิธานการดูแลผู้ป่วยในวันฮีโมฟีเลียโลก ในวาระครบรอบ 20 ปีของวันฮีโมฟีเลยโลก ไวเอท ฟาร์มาซูติคอลส์ (Wyeth Pharmaceuticals) บริษัทในเครือ ไวเอท (NYSE: WYE) จับมือกับองค์การฮีโมฟีเลียโลก (World Federation of Hemophilia หรือ WFH) ประกาศเปิดตัว 5 พันธมิตรใหม่ในโครงการ WFH Twinning Program ซึ่งเป็นโครงการที่ริเริ่มมาตั้งแต่ปี พ.ศ. 2537 และมีวัตถุประสงค์เพื่อพัฒนาคุณภาพการวินิจฉัยและรักษาผู้ป่วยโรคฮีโมฟีเลีย (โรคเลือดไหลไม่หยุด) ผ่านการประสานงานระหว่างศูนย์การแพทย์และองค์กร

New Partnerships Added to World Federation of Hemophilia Twinning Program

Wyeth and Advocacy Community Mark Continued Commitment to Patient Care on World Hemophilia Day In honor of the twentieth Anniversary of World Hemophilia Day, Wyeth Pharmaceuticals, a division of Wyeth (NYSE: WYE), together with...

Wyeth Pharmaceuticals and MediVas Announce Research Partnership to Develop Advanced Hemophilia Therapies

Wyeth World's Fourth Largest Biopharmaceutical Company Seeks to Further Its Innovation in Hemophilia As part of its ongoing commitment to provide advanced therapies for hemophilia, Wyeth...

Wyeth Receives Positive Opinion from European Regulators for its 13-valent Pneumococcal Candidate Vaccine for Infants and Young Children

Wyeth Pharmaceuticals, a division of Wyeth (NYSE: WYE), announced today that the European Medicines Agency's (EMEA) Committee for Medicinal Products for Human Use ...

วัคซีน Prevenar 13* ของไวเอทได้รับการอนุมัติให้ใช้สำหรับป้องกันโรคติดเชื้อนิวโมคอคคัสในทารกและเด็กเล็กเป็นครั้งแรก

ชิลีให้การอนุมัติวัคซีน Prevenar 13 เพื่อป้องกันโรคติดเชื้อนิวโมคอคคัสในทารกและเด็กเล็กเป็นครั้งแรก ไวเอท ฟาร์มาซูติคอลส์ (Wyeth Pharmaceuticals) ซึ่งเป็นบริษัทในเครือไวเอท (NYSE: WYE)...

Wyeth's Prevenar 13* Receives First Approval

-Chile Grants First Approval of Prevenar 13 for the Prevention of Pneumococcal Disease in Infants and Children- Wyeth Pharmaceuticals, a division of Wyeth (NYSE: WYE), announced today that the Chilean Ministry of Health, MINSAL (Ministerio de Salud), has...

ข้อมูลเบื้องต้นจากการวิจัย 2 ฉบับเผยประสิทธิภาพของการใช้ยา Neratinib ร่วมกับยา Trastuzumab และร่วมกับยา Paclitaxel ในผู้ป่วยมะเร็งทรวงอก HER-2 ขั้นรุนแรง

ไวเอท ฟาร์มาซูติคอลส์ (Wyeth Pharmaceuticals) ซึ่งเป็นบริษัทในเครือไวเอท (NYSE: WYE) ประกาศข้อมูลเบื้องต้นจากสองการวิจัยสำคัญ หนึ่งคือการประ...

New Preliminary Data from Two Studies Show Clinical Activity of Neratinib in Combination with Trastuzumab and in Combination with Paclitaxel in Advanced HER-2 Positive Breast Cancer

Wyeth Pharmaceuticals, a division of Wyeth (NYSE: WYE), today announced preliminary data from two ongoing studies, one...

สำนักงานอาหารและยาสหรัฐรับพิจารณา Prevnar 13 ก่อนอนุมัติเป็นยาตัวใหม่สำหรับโรคติดเชื้อนิวโมคอคคัส

ไวเอท ฟาร์มาซูติคอลส์ (Wyeth Pharmaceuticals) ซึ่งเป็นบริษัทในเครือไวเอท (NYSE: WYE) ประกาศว่า องค์การอาหารและยาสหรัฐ (FDA) กำลังอยู่ระหว่างพิจารณาสถานะยาให้กับ Prevnar 13* ซึ่งเป็นวัคซีนป้องกัน 13 ...