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Micrologix Biotech Inc. | BC Research Complex | 3650 Wesbrook Mall | Vancouver BC Canada V6S 2L2

FOR IMMEDIATE RELEASE TRADING SYMBOL: MBI (TSE/CDNX)
MGIXF (US over the counter)
Investor Relations Contact:
Arthur J. Ayres
Micrologix Biotech Inc.
Telephone: (604) 221-9666
Toll-Free: (800) 665-1968
Fax: (604) 221-9688
info@mbiotech.com

 
MICROLOGIX REPORTS FIRST QUARTER RESULTS

Vancouver, CANADA, September 12, 2000 - Micrologix Biotech Inc. today reported a loss of $1,752,766 or $0.05 per common share for the three months ended July 31, 2000, compared to a loss of $1,983,171 or $0.09 per common share for three months ended July 31, 1999.

The decrease in loss is due to the increase in interest income resulting from the Company's enhanced cash position and higher rates of return thereon. Interest income was $790,412 compared to $97,601 in 1999. At July 31, 2000, the Company's cash, cash equivalents and marketable securities were $54,941,873. Expenses increased 22% primarily due to the expansion and advancement of the Company's clinical development programs. Research and development expenses were $1,876,974, an increase of 29%. General and corporate costs increased 6% to $666,204.

During the quarter, the Company continued preparations for two pivotal phase III clinical trials of MBI 226 which is targeted at preventing catheter-related bloodstream infections. These studies are on track to start later this month. Additionally during the quarter, phase I studies were successfully completed for MBI 594AN in the treatment of acne and for MBI 853NL in the prevention of hospital-acquired infections caused by Staphylococcus aureus. Preparations are underway to initiate further clinical trials of MBI 594AN and MBI 853NL in the fourth quarter of 2000.

The Company's cash, cash equivalents and marketable securities decreased $1,667,959 during the quarter. This decrease consists of $1,779,124 used for operating activities, $378,573 to fund capital expenditures and $145,649 to fund expenses associated with the March special warrant financing, less $635,387 received from the exercise of warrants and stock options.

On August 30, 2000, the Company announced the receipt of approximately $8.6 million pursuant to the exercise of warrants and after-market support options increasing the Company's cash position to approximately $63 million. There are currently 39,311,809 (July 31, 2000 - 35,802,142) common shares issued and outstanding.

ANNUAL AND EXTRAORDINARY GENERAL MEETING

On September 7, 2000, Micrologix held its Annual and Extraordinary General Meeting. The Company's shareholders approved all resolutions including the adoption of the 2000 Incentive Stock Option Plan, an increase in the authorized capital and the adoption of the Shareholder Rights Plan announced August 9, 2000. Details of these matters were included in the Information Circular mailed to shareholders.

At the meeting, shareholders also elected the seven directors proposed by management. Re-elected were William (Bud) Foran, Chairman of the Board; Dany Hadary, Keith Dorrington, Steven Gillis, Colin Mallet and Robert Rieder. Joining the board is newly elected member David Scott. Mr. Scott, Chairman of AnorMED Inc., brings to Micrologix's board of directors over 30 years in investment analysis and management experience.

CORPORATE PROFILE

Micrologix Biotech Inc. develops novel drugs targeted at severe and life-threatening diseases-particularly those caused by antibiotic-resistant bacteria. The Company's portfolio of antibiotic drug candidates is based on improved analogs of naturally occurring cationic peptides found in the host defense systems of most life forms. Micrologix currently has three drugs in clinical trials in the US -- MBI 226 for the prevention of catheter-related bloodstream infections, MBI 594AN for the treatment of acne and MBI 853NL for the prevention of hospital-acquired Staphylococcus aureus infections. Under FDA fast track designation, the Company plans to initiate Phase III clinical trials of MBI 226 in September 2000. Micrologix recently completed Phase I clinical trials of MBI 594AN and MBI 853NL and anticipates initiating further clinical trials for these drug candidates during the fourth quarter of 2000.

The foregoing news release contains forward-looking statements within the meaning of the United States Private Securities Litigation Reform Act of 1995. All statements other than statements of historical fact may be deemed to be forward-looking statements. Forward-looking statements frequently, but not always use the words "expects", "anticipates", "suggests", "plans", "believes" or "intends", or similar words and/or include statements concerning the Company's strategies, goals and plans, or state that certain actions, events or results "will" be taken, occur or be achieved. These forward-looking statements involve known and unknown risks, uncertainties and other factors which may cause the actual results, performance or achievement of the company, or industry results, to be materially different from any future results, performance or achievements expressed or implied by such statements. Such factors include, among others those described in the Company's annual report on Form 20-F, including the following: uncertainties related to early stage of development, technology and product development; dependence on future corporate collaborations; dependence on proprietary technology and uncertainty of patent protection; management of growth; future capital needs and uncertainty of additional funding; intense competition; manufacturing and market uncertainties; government regulation; product liability exposure and insurability.

The Toronto Stock Exchange and the Canadian Venture Exchange have not reviewed and do not accept responsibility for the adequacy or accuracy of this release.

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