8-K 1 a51738e8vk.htm FORM 8-K e8vk
 
 
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): March 9, 2009
IDM PHARMA, INC.
(Exact name of registrant as specified in its charter)
         
Delaware   0-19591   33-0245076
(State or other jurisdiction   (Commission   (IRS Employer
of incorporation)   File Number)   Identification No.)
     
9 Parker, Suite 100
Irvine, California

(Address of principal executive offices)
  92618
(Zip Code)
Registrant’s telephone number, including area code (949) 470-4751
(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 (see General Instruction A.2. below):
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 March 9, 2009, IDM Pharma, Inc. (the “Company”) issued a press release announcing that the European Commission has formally granted a Centralized marketing authorization for mifamurtide (“L-MTP-PE”), known as MEPACT® in Europe, for the treatment of patients with non-metastatic, resectable osteosarcoma, a rare and often fatal bone tumor that typically affects children and young adults. The Centralized marketing authorization allows L-MTP-PE to be marketed in the 27 Member States of the European Union, as well as in Iceland, Liechtenstein and Norway. L-MTP-PE was granted orphan medicinal product status in Europe in 2004 and under European pharmaceutical legislation is entitled to a period of 10 years market exclusivity in respect of the approved indication.
A copy of this press release is attached as Exhibit 99.1 to this Current Report and is incorporated herein by reference.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits
     
Exhibit No.   Description
 
   
99.1
  IDM Pharma, Inc. press release.

 


 

SIGNATURES
     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.
         
  IDM PHARMA, INC.
 
 
Date: March 9, 2009  By:   /s/ Robert J. De Vaere    
    Robert J. De Vaere   
    Senior Vice President, Finance and Administration
and Chief Financial Officer 
 

 


 

         
INDEX TO EXHIBITS
     
Exhibit No.   Description
 
   
99.1
  IDM Pharma, Inc. press release.