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To: MMK who wrote (7295)2/2/1999 8:41:00 AM
From: dfund  Respond to of 56535
 
MMK: I admit I'm hooked but - WOW! - I didn't realize it was so obvious to everyone else! :-)

dfund



To: MMK who wrote (7295)2/2/1999 9:04:00 AM
From: MMK  Respond to of 56535
 
ALL: ASTM- FYI

I have a small long hold in this co. Gapping slightly in pre-market on the news. float- 6.10 mil. shares outstanding- 13.77

MMK

Tuesday February 2, 8:29 am Eastern Time

Company Press Release

SOURCE: Aastrom Biosciences, Inc.

Aastrom Biosciences Announces CE Mark
Approval For Cord Blood Therapy Kit

-- Cord Blood Transplantation Offers New Therapy Options for Patients with Cancer
and Other Diseases--

ANN ARBOR, Mich., Feb. 2 /PRNewswire/ -- Aastrom Biosciences, Inc. (Nasdaq: ASTM - news), today
announced that it has obtained approval to affix the CE Mark to the final components of the
AastromReplicell(TM) Cell Production System (System) CB-I Therapy Kit for the production of cord blood
cells used in stem cell therapy. This announcement follows earlier approvals received by Aastrom to affix the CE
Mark to the AastromReplicell(TM) System instrumentation platform and SC-I therapy kit for the production of
bone marrow cells used in stem cell therapy. These approvals allow marketing activities to begin for each of
these products in the European Community upon Aastrom's final product release.

''This most recent CE Mark approval demonstrates continued and steady progress at the Company to bring the
AastromReplicell(TM) System to the market in Europe and to enable new therapy approaches in the treatment
of cancer and other diseases,'' said R. Douglas Armstrong, Ph.D., President and Chief Executive Officer of
Aastrom. Dr. Armstrong continued, ''Importantly, the regulatory approval provided to the
AastromReplicell(TM) System may set a standard for the way cell therapy applications are regulated in Europe.
This regulatory process is directed at the manner in which the cells are manufactured rather than the cells
themselves. The therapy-specific kit approach offered by the AastromReplicell(TM) System not only enables
hospitals to have access to needed cells, but also provides both a standardized mechanism and increased
reliability for different treatment centers to carry out cell production for a variety of therapies.''

By being able to produce cord blood cells to larger quantities using the AastromReplicell(TM) System, patients
with blood cancers and diseases may have a new treatment option when an acceptable bone marrow donor
cannot be found, thereby yielding a new therapeutic approach for adult and pediatric patients with otherwise
incurable hematologic disorders. Cord blood, which remains in the umbilical cord and placenta after childbirth, is
a rich source of stem cells that can be used to restore tissue destroyed by aggressive chemotherapy or radiation
therapy used in the treatment of cancer and other diseases. While cord blood is emerging as a promising new
source of stem cells for use in therapy, there is unfortunately a limited quantity of cells available from a standard
cord blood collection, restricting the effectiveness of cord blood transplants. Low transplantation cell dose is
particularly problematic for larger and older patients where cord blood transplantation is generally not
attempted. The AastromReplicell(TM) System CB-I Therapy Kit is designed to address this limitation. The
Company recently reported positive clinical results at the Annual Meeting of the American Society of
Hematology from multi-center trials using the AastromReplicell(TM) System CB-I Therapy Kit to produce cord
blood cells used in the treatment of patients with cancer and other blood diseases.

The AastromReplicell(TM) System consists of an instrumentation platform designed to operate a family of
patient-specific cell therapy kits for a broad range of cell therapy applications. In addition to the currently used
stem cell therapies, many emerging cell therapies are being developed at academic centers and other companies.
The AastromReplicell(TM) System, an automated clinical system designed for the production of therapeutic cells
from small starting quantities, is designed to enable the transition of these laboratory procedures to a standard
medical treatment. Once established for use in stem cell therapy, Aastrom plans to leverage the cell
manufacturing capabilities of the AastromReplicell(TM) System across multiple cell therapy opportunities by
providing a commercialization outlet for these therapies through the AastromReplicell(TM) System product line.

Aastrom Biosciences, Inc. is pioneering the development of proprietary clinical systems including the
AastromReplicell(TM) System, a first of its kind product, to enable physicians and patients greater accessibility
to cells used for therapy. The AastromReplicell(TM) System product line consists of an instrumentation platform
that can operate a growing number of patient specific therapy kits tailored to each cell therapy application.
Aastrom has received patents covering methods and devices for the ex vivo production of human stem and other
types of cells, as well as for the genetic modification of stem cells. The AastromReplicell(TM) System is under
development, and is not available for sale at this time in the U.S.

This document contains forward-looking statements, including without limitation, statements concerning product
development objectives, clinical trial results, commercial introduction, and potential advantages of the
AastromReplicell(TM) System, which involve certain risks and uncertainties. The forward-looking statements
are also identified through use of the words ''anticipates,'' ''believes,'' ''expects,'' ''plans,'' 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 results obtained from clinical trial and
development activities, regulatory approval requirements, the availability of resources and the degree to which
the Company's products achieve market acceptance. These and other significant factors are discussed in greater
detail in Aastrom's Annual Report on Form-10K and other filings with the Securities and Exchange Commission.

SOURCE: Aastrom Biosciences, Inc.

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