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VOQP VioQuest Pharmaceuticals Inc (CE)

0.000001
0.00 (0.00%)
03 Dec 2024 - Closed
Delayed by 15 minutes
Share Name Share Symbol Market Type
VioQuest Pharmaceuticals Inc (CE) USOTC:VOQP OTCMarkets Common Stock
  Price Change % Change Share Price Bid Price Offer Price High Price Low Price Open Price Shares Traded Last Trade
  0.00 0.00% 0.000001 0.00 00:00:00

Vioquest Pharmaceuticals, Inc. - Current report filing (8-K)

11/09/2008 9:19pm

Edgar (US Regulatory)




UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549

FORM 8-K

CURRENT REPORT


PURSUANT TO SECTION 13 OR 15( d ) OF
THE SECURITIES EXCHANGE ACT OF 1934


Date of Report (Date of earliest event reported): September 10, 2008


VioQuest Pharmaceuticals, Inc.
(Exact name of registrant as specified in its charter)




Delaware
000-16686
58-1486040
(State or other jurisdiction of incorporation)
(Commission File Number)
(IRS Employer
Identification No.)
     
180 Mt. Airy Road, Suite 102
Basking Ridge, NJ 07920
(Address of principal executive offices)      


(908) 766-4400
(Registrant's telephone number, including area code)

N/A
(Former name or former address, if changed since last report)


Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

o
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
o
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
o
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
o
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))





 
 

 


Item 8.01
Other Events.

On September 9, 2008, VioQuest Pharmaceuticals, Inc. (the “Company”) received a determination from the U.S. Food and Drug Administration that Xyfid™ (1% uracil topical) is a drug rather than a device and would be regulated with the Center for Drug Evaluation and Research as opposed to the Center for Devices and Radiologic Health. Thus, Xyfid is not eligible for marketing clearance pursuant to the 510(k) process, but the Company will continue its parallel development of Xyfid for the prevention of hand-foot syndrome.
 
On September 10, 2008, the Company released the press release filed herewith as Exhibit 99.1 to this Current Report on Form 8-K and the press release is incorporated herein by reference.
 
Item 9.01
Financial Statements and Exhibits.

(d)   Exhibits
 
  Exhibit No. Description
     
99.1
Press release of the Company dated September 10, 2008.
 

 
 

 

SIGNATURE

Pursuant to the requirements of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
 
  VioQuest Pharmaceuticals, Inc.
   
     
Date: September 11, 2008
By:  
/s/ Christopher P. Schnittker
   

Christopher P. Schnittker
   
Vice President & Chief Financial Officer
   
 
 

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