| FOR
IMMEDIATE RELEASE AUTOIMMUNE
INC. REPORTS 2002 FIRST QUARTER AND YEAR END FINANCIAL RESULTS Pasadena,
California, May 9, 2002 AutoImmune Inc. (Nasdaq: AIMM)
today reported a net loss of $0.22 million, or $0.01 per share basic and diluted,
for the three months ended March 31, 2002, compared with a net loss of $0.12 million,
or $0.01 per share basic and diluted, for the three months ended March 31, 2001.
These results reflect the continued receipt of monthly payments from BioMS Medical
Corporation (BioMS), the reduction in patent expenses and a reduction
in interest income due to a lower average return on investment. As of March 31,
2002, the Company reported $10.6 million in cash and marketable securities.
Robert
C. Bishop, Ph.D., Chairman of the Board and Chief Executive Officer stated AutoImmune
is actively pursuing additional outlicensing opportunities and will continue to
conserve financial resources while waiting for results from externally funded
clinical trials.
BioMS Medical Corporation has said it anticipates
starting an advanced phase clinical trial during the latter part of 2002 on its
MBP8298 treatment for chronic progressive multiple sclerosis which utilizes intellectual
property rights exclusively licensed from AutoImmune. Teva Pharmaceutical Industries,
Ltd., has announced it will conduct additional pre-clinical and clinical pharmacology
studies on an oral formulation of COPAXONE® (glatiramer acetate), a product
for the treatment of multiple sclerosis, which utilizes intellectual property
rights exclusively licensed from AutoImmune. Recruitment for the NIH sponsored
diabetes prevention trial (DPT-1) remains ongoing.
AutoImmune is a biopharmaceutical
company involved in the development of a new class of mucosally administered therapies
for the treatment of autoimmune and cell-mediated inflammatory diseases and conditions.
This
release contains forward-looking statements which involve risks and uncertainties.
The Companys actual results may differ significantly from results discussed
in the forward-looking statements due to a number of important factors, including,
but not limited to the uncertainties of clinical trial results, the Companys
dependence on third parties for licensing revenue, and the risks of technological
change and competition. These factors are more fully discussed in the Companys
most recent Annual Report on Form 10-K filed with the Securities and Exchange
Commission in the section Business-Factors to be Considered. The discussion
in the Annual Report on Form 10-K is hereby referenced into this release. -
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