SI
SI
discoversearch

We've detected that you're using an ad content blocking browser plug-in or feature. Ads provide a critical source of revenue to the continued operation of Silicon Investor.  We ask that you disable ad blocking while on Silicon Investor in the best interests of our community.  If you are not using an ad blocker but are still receiving this message, make sure your browser's tracking protection is set to the 'standard' level.
Biotech / Medical : Pharmacyclics (PCYC) -- Ignore unavailable to you. Want to Upgrade?


To: Doug Meetmer who wrote (437)5/11/1999 9:23:00 AM
From: Biomaven  Read Replies (1) | Respond to of 717
 
Doug,

I can't say I share your pessimism on Antrin. I thought the results were actually pretty good, particularly for an early Phase I. This is the sort of procedure where fine tuning - drug dosage, light dosage, repeating the procedure and figuring out the right target population can have a very big impact on efficacy. (Remember also that the figures they quoted included some early patients where the drug dosage was too small for efficacy).

It's also important to realize that balloon angioplasty doesn't work well in patients where the disease is not localized to one area, as is often the case in peripheral artery disease.

I was impressed with how quickly they completed enrollment at their two trial locations - this is often a leading indicator of what the doctors at the trial locations think of the procedure.

Even if Antrin were successful, I wouldn't expect it to supplant existing methods; just supplement them. The market is big enough so that even a fairly small market share would have a substantial impact on a company PCYC's size.

I do agree that Antrin is still very early (and that Gd-Tex still has a fair way to go).

Peter