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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 FISCAL 2000 YEAR END RESULTS

Vancouver, CANADA, July 18, 2000 - Micrologix Biotech Inc. today reported a net loss of $8,659,873 or $0.32 per common share for the year ended April 30, 2000 ("Fiscal 2000"), compared to a net loss of $6,506,709 or $0.28 per common share for the year ended April 30, 1999 ("Fiscal 1999"). The net loss for the three months ended April 30, 2000 was $2,975,910 or $0.10 per common share compared to a net loss of $1,776,559 or $0.08 per common share for the same period in 1999.

"Micrologix achieved several major clinical milestones in Fiscal 2000 and I am confident that even more will be accomplished in the year ahead," said Dany Hadary, President and CEO of Micrologix. "Following the completion of Phase I, we received fast track designation from the FDA and successfully completed Phase II clinical trials for MBI 226, which is targeted at preventing catheter-related bloodstream infections, a very serious and often fatal medical condition for which effective therapeutic options are limited. Two additional drug candidates - MBI 594AN for the treatment of acne and MBI 853NL for the prevention of hospital-acquired infections caused by Staphylococcus aureus entered Phase I clinical trials. In the year ahead, we intend to move these three products into advanced-stage clinical trials, including MBI 226 into pivotal Phase III studies in the third quarter of 2000. These studies will form the basis for a New Drug Application to market MBI 226 in the United States."

At April 30, 2000 the Company's cash, cash equivalents and marketable securities were $56,609,832 an increase of $46,058,905 from April 30, 1999. This increase consists of $51,100,079 proceeds ($50,921,178 net of financing costs payable) from two equity financings completed during Fiscal 2000, $2,182,834 received from the exercise of after-market support options, warrants and stock options, less $6,699,999 used for operating activities and $524,009 to fund capital expenditures. There are currently 35,797,142 (April 30, 2000 - 31,536,517) common shares issued and outstanding.

Operating expenses in Fiscal 2000 increased 36% to $9,683,066, an increase of $2,550,177 compared with Fiscal 1999. This increase was principally due to the expansion and advancement of the Company's clinical development programs including the initiation and completion of the Phase II clinical trial for MBI 226 and preparations for Phase III, and the initiation of Phase I clinical trials for MBI 594AN and MBI 853NL. Clinical development program costs increased 135% to $3,376,880 in Fiscal 2000, an increase of $1,940,554 compared with Fiscal 1999. Other research and development expenses were $3,560,571 in Fiscal 2000 compared with $3,629,740 in Fiscal 1999. General and corporate expenses increased 33% to $2,745,615 in Fiscal 2000. Interest income was $1,023,193 in Fiscal 2000, an increase of $397,013 compared with Fiscal 1999, principally due to higher average cash balances.

 

At April 30

Balance Sheets

2000

1999

 

 

 

Cash, cash equivalents and marketable securities

$56,609,832

$10,550,927

Other current assets

167,351

239,939

Total current assets

56,777,183

10,790,866

Capital assets

2,156,795

2,706,103

Total assets

$58,933,978

$13,496,969

Current liabilities

$2,050,438

$1,029,849

Deferred rental inducement

¾

27,719

Shareholders’ equity2

56,883,540

12,439,401

Total liabilities and shareholders’ equity

$58,933,978

$13,496,969

 

Three months ended
April 30

Year ended
April 30

Statements of Loss and Deficit

2000

1999

2000

1999

 

 

 

 

 

Revenue: interest and sundry

$468,430

$125,547

$1,023,193

$626,180

 

 

 

 

 

Expenses

 

 

 

 

Research and development

2,430,976

1,328,196

6,937,451

5,066,066

General and corporate

1,013,364

573,910

2,745,615

2,066,823

 

$3,444,340

$1,902,106

$9,683,066

$7,132,889

 

 

 

 

 

Net loss

$(2,975,910)

$(1,776,559)

$(8,659,873)

$(6,506,709)

Deficit, beginning of period

(26,624,790)

(19,164,268)

(20,940,827)

(14,434,118)

Deficit, end of period

$(29,600,700)

$(20,940,827)

$(29,600,700)

$(20,940,827)

Net loss per common share3

$(0.10)

$(0.08)

$(0.32)

$(0.28)

Weighted average number of common shares outstanding

 

31,378,350

 

23,058,599

 

27,174,162

 

23,058,599

1 Condensed from the Company’s audited financial statements.

2 As at July 18, 2000 there are 35,797,142 common shares outstanding, warrants to acquire 3,316,250 common shares, after-market support options to acquire 849,832 common shares, options to acquire 2,253,301 common shares and other commitments to issue approximately 172,000 common shares outstanding.

3 Loss per share is based on the weighted average number of common shares outstanding during the period including the Company’s shares held in escrow. Since the Company’s stock options, special warrants, warrants, after-market support options and warrants are anti-dilutive, fully diluted loss per common share has not been presented.

The Company’s Annual General Meeting will be held on September 7, 2000 at 2:00 p.m. in the Cheakamus Room at the Waterfront Centre Hotel, Vancouver, British Columbia. The record date is July 31, 2000.

Micrologix Biotech Inc. is a biopharmaceutical company developing novel drugs to treat severe and life-threatening diseases-particularly those caused by antibiotic-resistant microorganisms. Micrologix’s portfolio of antibiotic drug candidates is based on improved analogs of the anti-infective peptides found in the host-defense systems of most life forms. These peptides overcome conventional antibiotic resistance and extensive research by Micrologix and independent researchers indicates that it will be extremely difficult for resistance to develop to them.

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 Vancouver Stock Exchange have not reviewed and do not accept responsibility for the adequacy or accuracy of this release.

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