Today’s guidance is essentially unchanged from DYAX’s 12/15/03 PR announcing U.S. orphan-drug status for DX-890 in CF. It looks like DYAX has a good chance to be the first to market in this orphan indication, which would confer seven years of marketing exclusivity. DX-890 also has CF orphan status in Europe. Despite a big rise in the past year, DYAX remains a pretty cheap stock; I don’t have any position at this time.
>> In collaboration with Debiopharm S.A., we will be announcing results from the Phase IIa study of DX-890 in children with CF in the very near term. Debiopharm is also planning to initiate a larger Phase II trial of DX-890 in CF in the second half of 2004. <<
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