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CommentWire
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Following poor first-year performance, Wyeth [WYE] and MedImmune [MEDI] have announced the dissolution of their FluMist partnership. If MedImmune is to achieve success with this product alone, it may need to rethink its premium pricing strategy.
Published By Datamonitor
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28 Apr 2004 |
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CommentWire
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Wyeth [WYE] and MedImmune's [MEDI] FluMist failed to secure indications for use in key target groups for influenza vaccine in the US. Recently released results suggest that their second generation product may enable the two companies to capitalize on more conventional influenza vaccine sectors.
Published By Datamonitor
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15 Oct 2003 |
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Expert View
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Although the contraceptive pill has been hugely successful, remembering to take it every day can be a problem. Alternative delivery methods such as implants and injections, meanwhile, have proved unpopular. The contraceptive patch could fill the middle ground, potentially cutting unwanted pregnancies - but will it? Datamonitor women's health analyst Jane Richardson cuts through the hype...
Published By Datamonitor
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28 Mar 2002 |
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CommentWire
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Intercell has acquired Iomai for $189 million, in a deal motivated by the Austrian company's desire to gain ownership of Iomai's traveler's diarrhea vaccine and transdermal delivery technology. With the potential to deliver both vaccine and adjuvant, independently, through Iomai's transdermal patch, Intercell's development of its proprietary adjuvant IC31 may also benefit from the technology.
Published By Datamonitor
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13 May 2008 |
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ResearchWire
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Published By Datamonitor
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09 Nov 2004 |
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CommentWire
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Published By Datamonitor
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16 May 2001 |
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CommentWire
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Novartis [NVS] has joined Mylan [MYL] and Schwarz [SRZG.F] in offering a generic version of blockbuster ulcer drug Prilosec in the US. The arrival of Novartis may open the floodgates for multiple generics in the ulcer drug market. Yet for companies launching generics before legal issues are settled, the risks are huge.
Published By Datamonitor
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27 Aug 2003 |
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Expert View
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Published By Datamonitor
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08 Jun 2001 |
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CommentWire
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Approval of Teva's [TEVA] olanzapine tablets is subject to the US District Court finding Lilly's [LLY] Zyprexa patent invalid. Furthermore, it is likely Teva will have to sit out a 180-day exclusivity period awarded to the first ANDA applicant. However, continued delays in the judge's decision make the outcome increasingly uncertain for Lilly.
Published By Datamonitor
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29 Mar 2005 |
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CommentWire
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The House of Lords committee was set up to review the ethical implications of allowing human embryonic cloning for research into degenerative diseases. Despite fierce campaigning by 'pro-life' groups, it came out in favor. Particularly after the recent restrictions imposed in the US, a 'reverse brain drain' of investment from the US to Europe could be on the cards.
Published By Datamonitor
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28 Feb 2002 |
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