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 : VD's Model Portfolio & Discussion Thread

 Public ReplyPrvt ReplyMark as Last ReadFilePrevious 10Next 10PreviousNext  
To: Vector1 who wrote (9622)6/19/2003 4:09:53 PM
From: tuck   of 9719
 
Nuts, your sell targets seem a bit optimistic now . . .

Should you manage to raise some cash somehow, perhaps a buying op coming in your old friend CBST? This came across the wires just after the bell today:

>>LEXINGTON, Mass.--(BUSINESS WIRE)--June 19, 2003--Cubist Pharmaceuticals, Inc. (Nasdaq: CBST - News) today announced that it has received notification from the U.S. Food & Drug Administration (FDA) that the agency now anticipates completing its priority review of the Cidecin® (daptomycin for injection) New Drug Application (NDA) on or before September 20, 2003, a three-month extension of tomorrow's original action date. Cubist continues to anticipate the approval and launch of CIDECIN by the end of 2003.
The extension is a result of the agency classifying a recent response to a question concerning the reformatting of certain data sets as a major amendment to the application. Under FDA standard operating procedures, the agency has reset the PDUFA (Prescription Drug User Fee Act) action date in order to review the reformatted data.

"As with any priority review, both the FDA and the sponsor are committed to working through a large number of issues during a very short period of time," said Cubist's President & CEO Michael W. Bonney. "We appreciate the agency's cooperative approach to working with us and believe this action to be the next best outcome to an approval. This submission of reformatted data sets resulted from interactions with the agency when unforeseen technical difficulties with the electronic submission became apparent, not from specific questions regarding the safety or efficacy of CIDECIN. We expect that these reformatted data sets will allow the agency to complete its priority review of this NDA by the new PDUFA action date and expect the impact on our launch timing to be minimal."

Cubist also announced today that the FDA has completed pre-approval inspections of daptomycin manufacturing facilities, and that previously scheduled labeling discussions have been postponed. Cubist anticipates these discussions will occur during the extension period.

CONFERENCE CALL & WEBCAST INFORMATION

WHEN: Thursday, June 19, 2003 at 5:00 pm ET

DOMESTIC & CANADA CALL-IN: (800) 915-4836
INTERNATIONAL CALL-IN: (973) 317-5319

CALL WILL ALSO BE BROADCAST LIVE, LISTEN ONLY, VIA THE WEB AT:

www.cubist.com

Replay will be available for 30 days via the Internet;
a transcript of the call will be filed with the SEC and will also
be available upon request<<

snip

Cheers, Tuck
Report TOU ViolationShare This Post
 Public ReplyPrvt ReplyMark as Last ReadFilePrevious 10Next 10PreviousNext