form8k20070604.htm


 
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):  May 29, 2007


Marshall Edwards, Inc.
(Exact name of registrant as specified in its charter)
 

 
Delaware
000-50484
 
51-0407811
(State or other jurisdiction of
incorporation or organization)
(Commission File Number)
(I.R.S. Employer Identification No.)


140 Wicks Road, North Ryde, NSW, 2113 Australia
(Address of principal executive offices) (Zip Code)
 
Registrant’s telephone number, including area code: (011) 61 2 8877-6196

Not Applicable
(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 CFR240.14d-2(b))

o                 Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR240.13e-4(c))

 
 


 
 
 
Item 5.02.                                Departure of Directors or Certain Officers; Election of Directors; Appointment ofCertain Officers; Compensatory Arrangements of Certain Officers.
 
 
On May 29, 2007, at a regularly scheduled meeting of the Board of Directors (the “Board”) of Marshall Edwards, Inc., Professor Graham E. Kelly retired as a member of the Board, effective May 29, 2007.  As a result of Professor Kelly’s retirement, the size of the Board has decreased from seven to six members.

 
 
 
Item 9.01.                                Financial Statements and Exhibits.

 
(d)           Exhibits.

Exhibit No.
Description
   
99.1
Press Release issued by Marshall Edwards, Inc. dated as of June 4, 2007


 
 
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.

 
MARSHALL EDWARDS, INC.


By:    /s/ David R Seaton
 
David R. Seaton
Chief Financial Officer
(Duly Authorized Officer and Principal
Financial Officer)


Dated: June 4, 2007

 

 
 
 


 
 Index to Exhibits
 
 
Exhibit No.
Description
   
99.1
Press Release issued by Marshall Edwards, Inc. dated as of June 4, 2007


 

 

ex99_1.htm
EXHIBIT 99.1
 
 
MARSHALL EDWARDS, INC.
Contacts:                      David Sheon
        202 518-6321
        dsheon@sciwords.com

                                      Chris Naughton
       011 61 2 9878 0088
       chris.naughton@marshalledwardsinc.com
                                      

NEWS RELEASE

For immediate release

COMPANY ANNOUNCEMENT

Washington June 4, 2007 - Professor Bryan Williams, Chairman of Marshall Edwards, Inc., has advised that Dr Graham Kelly has retired as a Director of the Company.

Professor Williams noted the significant contribution made by Dr Kelly to the development of the drugs now licensed by Marshall Edwards.

“His contribution to the development of the anti-cancer compound phenoxodiol in particular, is well known and acknowledged” Professor Williams said.

About phenoxodiol:
 
Phenoxodiol is being developed as a therapy for late-stage, chemo-resistant prostate, ovarian and cervical cancers.  Phenoxodiol is an investigational drug and, as such, is not commercially available.  It is a novel-acting drug that inhibits key pro-survival signaling pathways  operating via sphingosine-1-phosphate and Akt.  Inhibition of these pathways leads to prevention of phosphorylation of key anti-apoptotic proteins such as XIAP.  Loss of activity of these proteins restores the ability of chemoresistant tumor cells to undergo apoptosis in response to chemotherapy.  The putative molecular target for phenoxodiol is a tumor-specific protein, accounting for the highly selective nature of the drug.


About Marshall Edwards Inc:
 
Marshall Edwards, Inc. (Nasdaq : MSHL) is a specialist oncology company focused on the clinical development of novel anti-cancer therapeutics.  These derive from a flavonoid technology platform which has generated a number of novel compounds characterized by broad ranging efficacy against a range of cancer targets with few side effects.  The unique combination of efficacy and safety has been explained by their ability to target an enzyme present on the surface of cancer cells, thereby inhibiting the production of pro-survival proteins within the cell.  Marshall Edwards, Inc. has licensed rights from Novogen Limited (Nasdaq : NVGN) to bring three oncology drugs – phenoxodiol, NV-196 and NV-143 -  to market globally.  Marshall Edwards, Inc. is majority owned by Novogen, an Australian biotechnology company that is specializing in the development of therapeutics based on a flavonoid technology platform.  Novogen, based in Sydney, Australia, is developing a range of therapeutics across the fields of oncology, cardiovascular disease and inflammatory diseases.  More information on phenoxodiol and on the Novogen group of companies can be found at www.marshalledwardsinc.com and www.novogen.com.

 
Under U.S. law, a new drug cannot be marketed until it has been investigated in clinical trials and approved by the FDA as being safe and effective for the intended use. Statements included in this press release that are not historical in nature are "forward-looking statements" within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. You should be aware that our actual results could differ materially from those contained in the forward-looking statements, which are based on management's current expectations and are subject to a number of risks and uncertainties, including, but not limited to, our failure to successfully commercialize our product candidates; costs and delays in the development and/or FDA approval, or the failure to obtain such approval, of our product candidates; uncertainties in clinical trial results; our inability to maintain or enter into, and the risks resulting from our dependence upon, collaboration or contractual arrangements necessary for the development, manufacture, commercialization, marketing, sales and distribution of any products; competitive factors; our inability to protect our patents or proprietary rights and obtain necessary rights to third arty patents and intellectual property to operate our business; our inability to operate our business without infringing the patents and proprietary rights of others; general economic conditions; the failure of any products to gain market acceptance; our inability to obtain any additional required financing; technological changes; government regulation; changes in industry practice; and one-time events. We do not intend to update any of these factors or to publicly announce the results of any revisions to these forward-looking statements.