A blog about chemistry, drug development, science, and technology
I posted previously on Neurocrine and the insomnia drug Indiplon. There seems to be much more to the story than what I first thought. I concentrated on the information that the FDA hadn’t fully reviewed all the data and that the lower doses (in capsules) were given an approvable letter and the higher dose tablets were not. Now it seems Pfizer is ending their agreement with Neurocrine. Here’s the press release.
Neurocrine and Pfizer Terminate Collaboration Agreement for Indiplon
The Street.com has another article.
It should be noted that the FDA sending an approvable letter does not mean it is approved. It means that, provided the questions that the FDA may have are satisfied, they would then approve the drug. It seems they rejected the long lasting version (the tablets) and asked for more data on the lower dose fast acting version (the capsules).
Neurocrine had a webcast yesterday and they have a link on their website. I’ve not had a chance to listen to it (and probably won’t for reasons I’m not going into). My guess is without Pfizers support, that Neurocrine will discontinue their work on this drug. Also the area of sleeping pills is becoming competitive and I’m not sure how well they would be able to penetrate the market. I do want to disclose that I have been an occasional user of Ambien for a couple of years now.
It’s also interesting to note Forbes has been hinting that Pfizer may buy Sepracor who makes Lunesta. I’m not sure how much weight to put on this. If Pfizer is truly interested in getting into the insomnia market this may be a better route to get into this area.
More news results:
Technorati Tags: Indiplon, insomnia, Neurocrine, Pfizer, Sepracor
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QDIS: blogging about chemistry, drug development, science and technology.

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