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Indevus inks licensing pact, lands FDA deal

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Indevus Pharmaceuticals ended last week on the upbeat news that it had struck a licensing deal for one of its experimental therapies and worked out an advantageous arrangement with the FDA on another drug up for approval. The news sent the company's shares up 86 percent.

Teva signed on to develop the stuttering drug pagoclone in a deal which is worth up to $92.5 million for Indevus in milestone payments. Under certain circumstances the deal can be structured for a 50/50 royalty split.

On another front, Indevus announced that the FDA gave it a green light to submit additional data for the testosterone replacement therapy Nebido rather than mount a new trial for the therapy. The agency's concerns are centered on adverse reactions at the injection site. Indevus can now resubmit its applications in the first quarter of next year rather than face a lengthy delay for a new trial. An approval could come in the fourth quarter of 2009.

- check out the Indevus release regarding the licensing deal
- read the Indevus release regarding the FDA agreement

Related Articles:
Indevus shares plunge on approval delay
Indevus trumpets positive results of Nebido study (June 2007)


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More stories about Teva Pharmaceutical Industries   pagoclone   Nebido   Licensing deals   Indevus Pharmaceuticals   FDA   Biotech deals  

Comments

Although I don't agree with Indevus' assertion that Nebido needs to be injected once every 10 weeks, it will be a nice alternative to the gels/creams on the market. Injections every 4 weeks would be better for steady state testosterone levels.

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