Form 8-K Filing

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) August 15, 2011 


Aastrom Biosciences, Inc.
(Exact name of registrant as specified in its charter)


Michigan

0-22025

943096597
(State or other jurisdiction
of incorporation)
(Commission File Number) (IRS Employer Identification No.)



24 Frank Lloyd Wright Drive
P.O. Box 376
Ann Arbor, Michigan

48106
(Address of principal executive offices) (Zip Code)

Registrant's telephone number, including area code:   (734) 930-5555



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

Item 2.02. Results of Operations and Financial Condition.

On August 15, 2011 the Registrant issued a press release, a copy of which is attached hereto as Exhibit 99.1 and is incorporated herein by reference.

Item 9.01. Financial Statements and Exhibits.

    Exhibit 99.1.       Press release dated August 15, 2011


SIGNATURE

    Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the Registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

    Aastrom Biosciences, Inc.
(Registrant)

August 15, 2011
(Date)
  /s/   TIMOTHY M. MAYLEBEN
Timothy M. Mayleben
Chief Executive Officer and President


  Exhibit Index
  99.1 Press release dated August 15, 2011






Aastrom Biosciences Reports Operating Results for the Quarter and Six Months Ended June 30, 2011

EXHIBIT 99.1

Aastrom Biosciences Reports Operating Results for the Quarter and Six Months Ended June 30, 2011

ANN ARBOR, Mich., Aug. 15, 2011 (GLOBE NEWSWIRE) -- Aastrom Biosciences, Inc. (Nasdaq:ASTM), the leading developer of patient-specific, multicellular therapies for the treatment of severe chronic cardiovascular diseases, today reported operating results for the quarter and six months ended June 30, 2011.

"During the second quarter we reached two important milestones: the completion of the Phase 2b RESTORE-CLI clinical trial, which established clinical proof-of-concept in no-option CLI patients, and completion of the Special Protocol Assessment (SPA) process with the FDA for our Phase 3 clinical trial for ixmyelocel-T in patients with critical limb ischemia who have no other treatment options. We are planning to launch this pivotal Phase 3 clinical trial and advance it through the final stages of clinical development and regulatory review with the support of our outstanding clinical team and advisors," said Tim Mayleben, president and CEO of Aastrom.  "We look forward to presenting final 12-month results from the Phase 2b RESTORE-CLI study at the American Heart Association meeting on November 14th and the final 12-month results from the Phase 2 dilated cardiomyopathy surgical study at the Heart Failure Society of America meeting on September 19th."

As of June 30, 2011, the company had $18.5 million in cash and cash equivalents, compared to $31.2 million in cash and cash equivalents at December 31, 2010. For the quarter and six months ended June 30, 2011, cash expenses were $6.1 million and $12.7 million, respectively.

Research and development expenses for the quarter and six months ended June 30, 2011, were $5.3 million and $9.7 million, respectively, versus $3.6 million and $6.5 million for the same periods a year ago. The increase in research and development expenses for both periods was primarily attributable to the preparation for the Phase 3 clinical program for ixmyelocel-T, as well as an increase in non-cash stock-based compensation expense.

General and administrative expenses for the quarter and six months ended June 30, 2011, were $2.2 million and $4.1 million, respectively, compared to $1.5 million and $2.9 million for the same periods a year ago.  The increase in general and administrative expenses for both periods was primarily due to an increase in regulatory, legal and employee-related expenses, including non-cash stock-based compensation expense. The increase in the six months ended June 30, 2011, compared to a year ago was also driven by the previously announced restatement of the company's historical financial results in the first quarter of 2011.

Other income (expense) for the quarter and six months ended June 30, 2011, was $(2.5) million and $(1.2) million, respectively, compared to $1.4 million and $2.9 million for the same periods a year ago. These fluctuations were due to non-cash changes in the fair value of the company's outstanding warrants, driven by an increase in the fair market value of the company's common stock during these periods.

Net loss for the quarter and six months ended June 30, 2011, was $10.0 million, or $0.26 per share, and $15.0 million, or $0.39 per share, respectively, compared to a net loss of $3.8 million, or $0.13 per share, and $6.5 million, or $0.23 per share, for the same periods a year ago.

As of June 30, 2011, Aastrom had 38.6 million shares of common stock outstanding. 

About Aastrom Biosciences

Aastrom Biosciences is the leader in developing patient-specific, expanded multicellular therapies for use in the treatment of severe, chronic cardiovascular diseases.  The company's proprietary cell-processing technology enables the manufacture of ixmyelocel-T, a patient-specific multicellular therapy expanded from a patient's own bone marrow and delivered directly to damaged tissues.  Aastrom has advanced ixmyelocel-T into late-stage clinical development, including a planned Phase 3 clinical program to study patients with critical limb ischemia and two Phase 2 clinical trials in patients with dilated cardiomyopathy. For more information, please visit Aastrom's website at www.aastrom.com.

The Aastrom Biosciences, Inc. logo is available at http://www.globenewswire.com/newsroom/prs/?pkgid=3663

This document contains forward-looking statements, including, without limitation, statements concerning clinical trial plans and progress, objectives and expectations, clinical activity timing, intended product development, the performance and contribution of certain individuals and expected timing of collecting and analyzing treatment data, all of which involve certain risks and uncertainties. These statements are often, but are not always, made through the use of words or phrases such as "anticipates," "intends," "estimates," "plans," "expects," "we believe," "we intend," and similar words or phrases, or future or conditional verbs such as "will," "would," "should," "potential," "could," "may," or similar expressions. Actual results may differ significantly from the expectations contained in the forward-looking statements. Among the factors that may result in differences are the inherent uncertainties associated with clinical trial and product development activities, regulatory approval requirements, competitive developments, and the availability of resources and the allocation of resources among different potential uses. These and other significant factors are discussed in greater detail in Aastrom's Annual or Transition Report on Form 10-K or 10-K/T, Quarterly Reports on Form 10-Q and other filings with the Securities and Exchange Commission. These forward-looking statements reflect management's current views and Aastrom does not undertake to update any of these forward-looking statements to reflect a change in its views or events or circumstances that occur after the date of this release except as required by law.

AASTROM BIOSCIENCES  
(in thousands, except per share amounts)  
   
CONDENSED CONSOLIDATED BALANCE SHEETS (Unaudited)
 
 
   
  December 31, June 30,  
  2010   2011  
ASSETS        
 Cash and cash equivalents $ 31,248   $ 18,521  
 Other current assets  451    524  
 Property and equipment, net  1,128    1,259  
 Total assets $ 32,827   $ 20,304  
         
LIABILITIES AND SHAREHOLDERS' EQUITY (DEFICIT)        
 Warrant liabilities $ 25,954   $ 27,164  
 Other current liabilities  3,910    3,255  
 Long-term debt  41    43  
 Shareholders' equity (deficit)  2,922    (10,158)
 Total liabilities and shareholders' equity (deficit) $ 32,827   $ 20,304  
 
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS (Unaudited)
 
 
 
  Quarter Ended
June 30,
Six Months Ended
June 30,
   2010    2011    2010    2011  
         
REVENUES  . $ -- $  -- $ -- $ 9
         
COSTS AND EXPENSES        
 Cost of product sales and rentals -- -- -- 2
 Research and development 3,619 5,304 6,464 9,676
 Selling, general and administrative  1,521  2,203  2,939  4,098
 Total costs and expenses  5,140  7,507  9,403  13,776
         
LOSS FROM OPERATIONS (5,140) (7,507) (9,403) (13,767)
         
OTHER INCOME (EXPENSE)        
 (Increase) decrease in fair value of warrants    1,348  (2,465) 2,907  (1,210)
 Other income, net 25 15 50 32
 Total other income (expense)  1,373  (2,450)  2,957  (1,178)
         
NET LOSS $ (3,767) $ (9,957) $ (6,446) $ (14,945)
         
NET LOSS PER SHARE
 (Basic and Diluted)
 
$ (0.13)
 
$ (0.26)
 
$ (0.23)
 
$ (0.3)
           
Weighted average number of common 
 shares outstanding (Basic and Diluted)
 
28,256
 
38,622
 
27,500
 
38,619
CONTACT: Media contact
         Bill Berry
         Berry & Company
         bberry@berrypr.com
         (212) 253-8881

         Investor contact
         Danielle Spangler
         The Trout Group
         dspangler@troutgroup.com
         (646) 378-2924