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 : Alexion Pharmaceuticals, Inc. (ALXN) -- Ignore unavailable to you. Want to Upgrade?


To: keokalani'nui who wrote (295)8/5/2003 2:05:19 PM
From: Ian@SI  Respond to of 824
 
Alexion Shares Tumble on Disappointing Study Results

djones

Dow Jones Newswires

NEW YORK -- Alexion Pharmaceuticals Inc. (ALXN) Chief Executive Leonard Bell said there's a "pretty remote possibility" that the Food and Drug Administration will say its first drug is not approvable, even though it failed to meet its primary endpoint in a large Phase III clinical trial.

The more likely scenario for the drug, called pexelizumab and studied in patients undergoing coronary artery bypass graft surgery, will be that the FDA might ask the company to run another Phase III, or late-stage, trial or that the
data from earlier trials and a secondary-endpoint analysis of the recent trial is enough for approval.

Investors aren't pleased, though, sending the stock down $3.48, or 22%, to $12.52 at around 10:30 a.m. EDT on the Nasdaq Stock Market. Volume was more than 1.9 million shares, compared with the 154,786 that cross the tape on an average
full trading day.

The company plans to discuss the data with its marketing partner Procter & Gamble Pharmaceuticals, the drug unit of Procter & Gamble Co. (PG), and the FDA.

If the agency asks the company to run another clinical trial, P&G would share the costs 50-50, Mr. Bell said.

The news, released late Monday, didn't include the actual data from the Phase III trial. That will be made public at the annual meeting of the American Heart Association in Orlando this November.

The company did say the drug failed to meet its primary endpoint of reducing the incidence of death or heart attacks within 30 days of a patient undergoing coronary artery bypass graft surgery without a valve operation.

However, the company did test the drug on sicker patients who had to undergo procedure and valve surgery. When including those patients, the study did satisfy statistical requirements in cutting down on heart attacks and death, but
that was only a secondary endpoint.

The data was reviewed by data safety monitoring board which brought up no specific issues from the trial, Mr. Bell said.

Alexion's President and Operating Chief David W. Keiser said that at this time the company, which is years away from profitability, should have a burn rate similar to the past year.

The company has $210 million in cash, he said.

In the nine months ended April 30, the company posted a loss of $62.9 million.



To: keokalani'nui who wrote (295)8/5/2003 5:11:09 PM
From: Ian@SI  Read Replies (1) | Respond to of 824
 
I just listened to the replay of this morning's conference call. Call is about 48 minutes long.

It was quite positive and optimistic -- much to my surprise. I had expected more negativity both from the company and from the Institutions. I took several notes which I'll probably share with the thread after dinner tonight or sometime tomorrow.

For those who are interested in listening firsthand, toll free access in North America is at: 1 888 203 1112 PASSCODE: 501849#

Following the passcode you will asked to provide something that makes the equipment think you're leaving your Name, Affiliation and Phone number followed by pressing the # symbol again.

If others do listen to the call, I'd appreciate hearing their impressions of it.

Thanks,
Ian