Xenova/QLT: tackling multidrug resistance

UK biotech Xenova and its North American ally QLT will trial tariquidar for multidrug resistance in non-small cell lung cancer. As long as the results are positive, tariquidar should have a bright future: multidrug resistance is an increasingly serious problem in cancer treatment, and the developers look set to provide strong marketing support.

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Wyeth: UK offers Efexor relief

Having concluded a new review of the latest safety evidence related to Wyeth's serotonin and noradrenergic reuptake inhibitor Efexor, UK regulators have eased the barriers restricting use of the drug. The updated prescribing advice should help Wyeth stabilize sales of Efexor while also enabling the company to plan more effectively for the launch of its follow-on compound, desvenlafaxine.

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Wyeth: positive Aprela results bode well for planned portfolio strategy

Wyeth has announced new positive Phase III data for its menopause treatment Aprela. The potential blockbuster is well positioned to provide a unique approach to the treatment of menopausal symptoms in women at risk of developing osteoporosis, and assuming regulatory hurdles can be overcome, Aprela will help further maintain Wyeth's position as a leading women's health player.

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Wyeth: diversity key to growth

Wyeth's performance in 2002 was negatively affected by its heavy reliance on its Women's Health franchise. With the anticipated launch of Flumist, it is expected that 2003 will mark the beginning of Wyeth's transition from a reliance on HRT treatments to a more diversified portfolio.<BR />

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Women's mental health: no easy thinking, no easy solutions

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Women's health: more HPV risk than expected

In the new survey, featuring women in their first relationship, 74% of respondents reportedly used barrier contraception. Yet nearly half developed some form of HPV infection. Companies such as Merck and Origenix, with vaccines in development for the virus, are likely to see significant revenues when their products hit the market.

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Vinka alkaloids: market to fall 17% by 2007

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Vernalis: revised R&D focus after Frova decision hits home

Vernalis's decision to undergo major restructuring is a direct result of the non-approval of the company's sNDA submission for Frova, for the treatment of menstrual migraine. A successful application had been anticipated to double the revenue potential of Frova.

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Vernalis: Frovelan concerns a headache for shareholders

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Vernalis: benefiting from SB's regulatory headaches

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