Aastrom Biosciences, Inc.
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):
February 7, 2007
Aastrom Biosciences, Inc.
(Exact name of registrant as specified in its charter)
|
|
|
|
|
Michigan
(State or other
jurisdiction of
incorporation)
|
|
0-22025
(Commission File No.)
|
|
94-3096597
(I.R.S. Employer
Identification No.) |
24 Frank Lloyd Wright Drive
P.O. Box 376
Ann Arbor, Michigan 48106
(Address of principal executive offices)
Registrants telephone number, including area code:
(734) 930-5555
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))
TABLE OF CONTENTS
Item 2.02 Results of Operations and Financial Condition.
On February 7, 2007, we issued a press release announcing financial results and achievements for
our second fiscal quarter ended December 31, 2006. A copy of the press release is attached hereto
as Exhibit 99.1.
Pursuant to General Instruction B.2 of Form 8-K, this report and the exhibit are not deemed to be
filed for purposes of Section 18 of the Securities Exchange Act of 1934, nor shall this report
and the exhibit be incorporated by reference into our filings under the Securities Act of 1933 or
the Securities Exchange Act of 1934, except as expressly set forth by specific reference in such
future filing.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits.
|
|
|
Exhibit No. |
|
Description |
99.1
|
|
Press Release dated February 7, 2007 |
2
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.
Date: February 7, 2007
|
|
|
|
|
|
AASTROM BIOSCIENCES, INC.
|
|
|
By: |
/s/ Gerald D. Brennan, Jr.
|
|
|
|
Gerald D. Brennan, Jr. |
|
|
|
Vice President Administrative &
Financial Operations and CFO |
|
|
3
Exhibit 99.1
EXHIBIT 99.1
FOR IMMEDIATE RELEASE
|
|
|
|
|
CONTACTS:
|
|
Kris M. Maly
Investor Relations Department
Aastrom Biosciences, Inc.
Phone: (734) 930-5777
|
|
Cameron Associates
Kevin McGrath
Phone: (212) 245-4577
Deanne Eagle (Media)
Phone: (212) 554-5463 |
Aastrom Reports Second Quarter Fiscal Year 2007 Financial Results
Ann Arbor, Michigan, February 7, 2007 Aastrom Biosciences, Inc. (Nasdaq: ASTM), a company
developing cell-based therapeutics for regenerative medicine, today reported financial results for
the second fiscal quarter ended December 31, 2006. The Company also reported operational
achievements during the quarter, including:
|
|
|
Senior management appointments |
|
|
|
Ronnda L. Bartel, Ph.D. as Vice President, Research & Development. Dr.
Bartel is responsible for the product development and manufacturing of Aastroms
Tissue Repair Cell-based (TRC) cell products, and the Companys discovery and
research efforts. |
|
|
|
|
Sheldon A Schaffer, Ph.D. as Vice President, Corporate Development &
Intellectual Property, a newly created position. Dr. Schaffer is responsible for
the development of corporate partnering and licensing opportunities, as well as the
expansion of Aastroms intellectual property portfolio. |
In addition, the Company has achieved the following clinical milestones during fiscal year 2007:
|
|
|
Completed patient enrollment in the EU Phase I/II long bone fracture clinical trial |
|
|
|
|
Initiated patient enrollment and treatments in the pivotal osteonecrosis clinical trial
in Spain |
|
|
|
|
Received Orphan Drug Designation from the FDA for the treatment of dilated
cardiomyopathy |
During this fiscal year we have strengthened our management team and accomplished several key
clinical milestones. Each of these milestones are critical to achieving our overall corporate goal
of advancing our clinical programs through the regulatory process and delivering cell therapies for
regenerative medicine, said George Dunbar, Chief Executive Officer and Chairman of Aastrom.
Since the beginning of calendar year 2007, we have initiated and treated patients in our adult
stem cell clinical trial for osteonecrosis in Spain, and received an orphan drug designation from
the FDA for dilated cardiomyopathy, a severe chronic disease of the heart. We look forward to
reporting on the clinical progress we have planned for the remainder of 2007.
Second Fiscal Quarter Ended December 31, 2006 Results
Total revenues for the quarter and six months ended December 31, 2006, consisting of limited
therapy kit sales for research by others and grant funding, were $158,000 and $262,000,
respectively, compared to $117,000 and $297,000 for the same periods in fiscal year 2006.
Total costs and expenses for the quarter and six months ended December 31, 2006 increased to
$4,898,000 and $9,586,000, respectively, from $4,456,000 and $8,430,000 for the same periods in
fiscal year 2006.
-more-
Aastrom- 2nd Q FY2007 Fin Results
February 7, 2007
Page 2
Research and development expenses for the quarter and six months ended December 31, 2006 increased
to $2,563,000 and $4,867,000, respectively, from $2,195,000 and $4,148,000 for the same periods in
fiscal year 2006. These increases reflect continued expansion of our research and development
activities to support future regulatory submissions, on-going and planned tissue regeneration
clinical trials in the U.S. and EU and the development of facilities for product manufacturing.
Research and development expenses for the quarter and six months ended December 31, 2006, also
include a non-cash charge of $181,000 and $290,000, respectively, compared to $121,000 and $199,000
for the same periods in fiscal year 2006, relating to share-based compensation expense.
Selling, general and administrative costs for the quarter and six months ended December 31, 2006
increased to $2,332,000 and $4,716,000, respectively, from $2,257,000 and $4,273,000 for the same
periods in fiscal year 2006. For the quarter and six months ended December 31, 2006, these
increases include a non-cash charge of $690,000 and $1,152,000, respectively, compared to $185,000
and $303,000 for the same periods in fiscal year 2006, relating to share-based compensation
expense. The increases in non-cash charges include a one-time non-cash charge of $257,000 that
relates to an amendment of the former CEOs consulting agreement. In addition, for the six months
ended December 31, 2006, the increase includes an accrual relating to the former CEOs revised
employment agreement, and an accrual and severance payments relating to the former President and
COOs employment agreement.
Interest income for the quarter and six months ended December 31, 2006 increased to $515,000 and
$1,042,000, respectively, from $197,000 and $503,000 for the same periods in fiscal year 2006. The
fluctuations in interest income are due primarily to corresponding changes in the level of cash,
cash equivalents and short-term investments during the periods, and to improved yields from our
investments.
Net loss for the quarter ended December 31, 2006 was $4,225,000, or $.04 per share, compared to a
net loss of $4,142,000, or $.04 per share for the same period in fiscal year 2006. Net loss for
the six months ended December 31, 2006, was $8,282,000, or $.07 per share, compared to $7,630,000,
or $.07 per share for the same period in fiscal year 2006. The increases in net loss are primarily
the result of increased costs and expenses offset on a per share basis by an increase in the
weighted average number of common shares outstanding.
At December 31, 2006, the Company had $36.3 million in cash, cash equivalents and short-term
investments as compared to $43 million at June 30, 2006.
Aastrom Conference Call Information
George W. Dunbar, President and Chief Executive Officer, Gerald D. Brennan, Jr., Vice President
Administrative & Financial Operations and Chief Financial Officer, and Elmar R. Burchardt, M.D.,
Ph.D., Vice President Medical Affairs of Aastrom Biosciences, Inc., will host a conference call to
review and discuss the second quarter fiscal year 2007 financial results at 9:00 a.m. (EST) today,
February 7, 2007. Interested parties should call toll-free (877) 407-9205, or from outside the
U.S. (201) 689-8054, fifteen minutes before the start of the call to register and identify
themselves as registrants of the Aastrom Conference Call. Any registered caller on the toll-free
line may ask to be placed in the queue for the Question & Answer session. The call will be
simulcast on the web at http://www.vcall.com/IC/CEPage.asp?ID=113519. A podcast of the call may be
downloaded from the web at the internet address above. If you are unable to participate during the
live call, the webcast will be available for replay at http://www.investorcalendar.com/ for 60
days. Also, through February 17, 2007, an audio replay of the call will be available by dialing
toll-free (877) 660-6853, or from outside the U.S. (201) 612-7415; when prompted on the phone line,
the Account # is: 286 and the Conference ID# is: 230316.
-more-
Aastrom- 2nd Q FY2007 Fin Results
February 7, 2007
Page 3
About Aastrom Biosciences, Inc.
Aastrom Biosciences, Inc. develops autologous cell products for the repair or regeneration of
multiple human tissues, based on its proprietary Tissue Repair Cell (TRC) technology. Aastroms
TRC-based products are a unique cell mixture containing stem and progenitor cell populations,
produced from a small amount of bone marrow taken from the patient. TRC-based products have been
used in over 240 patients, and are currently in clinical trials for bone regeneration
(osteonecrosis of the femoral head, long bone fractures and spine fusion) and vascular regeneration
(critical limb ischemia) applications. Aastrom has reported positive interim clinical trial
results for TRCs suggesting both the clinical safety and the ability of TRCs to promote healing in
bone regeneration applications. The Company is also developing programs for TRC-based therapies to
address cardiac and neural regeneration indications. TRCs have received Orphan Drug Designation
from the FDA for use in the treatment of osteonecrosis of the femoral head and the treatment of
dilated cardiomyopathy, a severe chronic disease of the heart.
For more information, visit Aastroms website at www.aastrom.com. (astmf)
This document contains forward-looking statements, including without limitation, statements
concerning clinical trial plans and expectations, intended product development and
commercialization objectives, expected milestones, plans for the current fiscal year and potential
product applications, which involve certain risks and uncertainties. The forward-looking
statements are also identified through use of the words planned, should and other words of
similar meaning. 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, the availability of resources and the allocation of resources among
different potential uses. These and other significant factors are discussed in greater detail in
Aastroms Annual Report on Form 10-K and other filings with the Securities and Exchange Commission.
Financial Table Follows
AASTROM BIOSCIENCES, INC.
(Unaudited)
(In thousands, except per share amounts)
CONSOLIDATED STATEMENTS OF OPERATIONS DATA:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Quarter ended December 31, |
|
|
Six months ended December 31, |
|
|
|
2005 |
|
|
2006 |
|
|
2005 |
|
|
2006 |
|
REVENUES: |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total revenues |
|
$ |
117 |
|
|
$ |
158 |
|
|
$ |
297 |
|
|
$ |
262 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
COSTS AND EXPENSES: |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cost of product sales |
|
|
4 |
|
|
|
3 |
|
|
|
9 |
|
|
|
3 |
|
Research and development |
|
|
2,195 |
|
|
|
2,563 |
|
|
|
4,148 |
|
|
|
4,867 |
|
Selling, general and administrative |
|
|
2,257 |
|
|
|
2,332 |
|
|
|
4,273 |
|
|
|
4,716 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total costs and expenses |
|
|
4,456 |
|
|
|
4,898 |
|
|
|
8,430 |
|
|
|
9,586 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
OTHER INCOME |
|
|
197 |
|
|
|
515 |
|
|
|
503 |
|
|
|
1,042 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
NET LOSS |
|
$ |
(4,142 |
) |
|
$ |
(4,225 |
) |
|
$ |
(7,630 |
) |
|
$ |
(8,282 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
NET LOSS PER COMMON SHARE |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
(Basic and Diluted) |
|
$ |
(.04 |
) |
|
$ |
(.04 |
) |
|
$ |
(.07 |
) |
|
$ |
(.07 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Weighted average number of common shares
outstanding |
|
|
102,681 |
|
|
|
119,516 |
|
|
|
102,582 |
|
|
|
119,347 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
CONSOLIDATED BALANCE SHEET DATA:
|
|
|
|
|
|
|
|
|
|
|
June 30, |
|
|
December 31, |
|
|
|
2006 |
|
|
2006 |
|
ASSETS |
|
|
|
|
|
|
|
|
Cash and cash equivalents |
|
$ |
9,034 |
|
|
$ |
13,979 |
|
Short-term investments |
|
|
33,963 |
|
|
|
22,333 |
|
Receivables, net |
|
|
139 |
|
|
|
121 |
|
Inventories |
|
|
1 |
|
|
|
12 |
|
Other current assets |
|
|
528 |
|
|
|
518 |
|
Property and equipment, net |
|
|
1,216 |
|
|
|
1,277 |
|
|
|
|
|
|
|
|
Total assets |
|
$ |
44,881 |
|
|
$ |
38,240 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
LIABILITIES AND SHAREHOLDERS EQUITY |
|
|
|
|
|
|
|
|
Current liabilities |
|
$ |
2,539 |
|
|
$ |
2,317 |
|
Shareholders equity |
|
|
42,342 |
|
|
|
35,923 |
|
|
|
|
|
|
|
|
Total liabilities and shareholders equity |
|
$ |
44,881 |
|
|
$ |
38,240 |
|
|
|
|
|
|
|
|
###