| FOR IMMEDIATE RELEASE |
TRADING SYMBOL: MBI (TSE/CDNX)
MGIXF (US over the counter)
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Investor Relations Contacts:
Art Ayres
Micrologix Biotech Inc.
Telephone: 604.221.9666
Toll-Free: 1.800.665.1968
aayres@mbiotech.com
Website
www.mbiotech.com
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Marla Gale
Fleishman-Hillard Canada Inc.
Telephone: 416.214.0701
Fax: 416.214.0720
galem@fleishman.com
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Micrologix Reports
Year-End Results
Fiscal 2001 a Year
of Progress
Vancouver, CANADA, July 19, 2001 – Micrologix
Biotech Inc. today reported financial results for the fourth quarter and
twelve months ended April 30, 2001 ("Fiscal 2001").
Fourth Quarter Highlights
- Continued to enroll patients in US FDA fast-tracked Phase III clinical
trial of MBI 226 and Phase II trial of MBI 594AN
- Granted two patents covering the compositions of 46 novel peptides and
their chemical derivatives designed for unique activity against bacteria and
fungi
- Announced executive appointments to strengthen the company’s
management team
- Appointed Ken Galbraith, former Executive V.P. and Chief Financial
Officer of QLT Inc., to the Board of Directors
"Fiscal 2001 was a year of significant progress as we advanced our two
leading drug candidates through clinical trials," said William (Bud)
Foran, Chairman and CEO of Micrologix. "In the next two weeks, we will
enroll the final patients in our Phase II trial for MBI 594AN, a compound that
treats acne. We expect to complete this study in September and results should
be available before the end of November. Recent positive preclinical data,
showing the significant anti-inflammatory activity of our peptides, further
support MBI 594AN as an effective acne treatment. As for our Phase III trial
of MBI 226 (a drug designed to prevent catheter-related bloodstream
infections), patient enrollment should be completed by the end of 2001 and we
expect to file a New Drug Application for U.S. marketing approval in the
second half of 2002."
" In addition to the solid clinical
progress made last year," added Mr. Foran, "we strengthened the
Company’s operations in other areas. We remain well funded and ended the
year with $55.8 million in cash and short-term investments. Through internal
R&D and our collaboration with the Harbor-UCLA Research and Education
Institute, we identified more compounds that will help us build a strong
product pipeline for the future."
"While our search for a new CEO is taking longer than expected, we are
confident that our prudent approach will help us identify the right leader to
guide Micrologix and build on the Company’s strengths. The year ahead will
be an exciting one as we continue to build solid relationships with potential
strategic partners and advance our clinical and research programs," Mr.
Foran concluded.
For the three months ended April 30, 2001, Micrologix reported a loss of
$4.3 million or $0.11 per share, compared to $3.0 million or $0.10 per share
for the same period in 2000. The loss for the twelve months ended April 30,
2001 was $11.7 million or $0.31 per share, compared to a loss of $8.7 million
or $0.34 per share for the same period in 2000.
Selected Financial Highlights (Canadian dollars) (1)
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Balance Sheets |
April 30, 2001 |
April 30, 2000 |
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ASSETS |
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Cash and cash equivalents |
$ 9,952,737 |
$45,014,873 |
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Short-term investments(2) |
45,839,031 |
11,594,959 |
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Other current assets |
405,944 |
167,351 |
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Total current assets |
$56,197,712 |
$56,777,183 |
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Capital assets |
1,598,784 |
1,346,719 |
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Intangible assets |
1,752,666 |
810,076 |
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Total assets |
$59,549,162 |
$58,933,978 |
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LIABILITIES & SHAREHOLDERS’ EQUITY |
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Current liabilities |
$ 4,523,321 |
$ 2,050,438 |
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Shareholders’ equity |
55,025,841 |
56,883,540 |
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Total liabilities and shareholders’ equity |
$59,549,162 |
$58,933,978 |
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Statements of Loss and Deficit |
Three months ended
April 30 |
Year ended
April 30 |
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2001 |
2000 |
2001 |
2000 |
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Revenue |
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Interest income
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$ 779,093 |
$ 468,430 |
$3,234,574 |
$1,023,193 |
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Expenses |
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Research and development |
3,864,115 |
2,430,976 |
11,145,489 |
6,937,451 |
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General and corporate |
1,172,165 |
1,013,364 |
3,797,791 |
2,745,615 |
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$5,036,280 |
$3,444,340 |
$14,943,280 |
$9,683,066 |
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Loss per common share |
$(4,257,187) |
$(2,975,910) |
$(11,708,706) |
$(8,659,873) |
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Deficit, beginning of period |
(37,052,219) |
(26,624,790) |
(29,600,700 |
(20,940,827) |
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Deficit, end of period |
$(41,309,406) |
$(29,600,700) |
$(41,309,406) |
$(26,600,700) |
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Loss per common share(3) |
$(0.11) |
$(0.10) |
$(0.31) |
$(0.34) |
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Weighted average number of common shares outstanding(3) |
38,165,620 |
29,960,817 |
37,246,047 |
25,756,628 |
1 Condensed from the Company’s
audited financial statements.
2 Short-term investments represent
investments in highly liquid interest bearing financial instruments with a
maturity date at the time of purchase greater than three months
3 Loss per share is based on the
weighted average number of common shares outstanding during the period.
Effective February 1, 2001 the Company adopted the new CICA recommendations for
the calculation of earnings per share. The impact of this change in accounting
policy is to exclude the Company’s escrow shares from the weighted average
number of common shares outstanding during the period. For the twelve months
ended April 30, 2001 this change resulted in a $0.01 (2000: $0.02) increase in
the loss per common share. Since the Company’s escrow shares, aftermarket
support options and stock options are anti-dilutive, fully diluted loss per
common share has not been presented.
Interest income for the twelve months increased to $3.2
million compared with $1.0 million in 2000, due to higher rates of return
and higher average cash reserves. Total operating expenses for the twelve
months increased 54 percent to $14.9 million compared with $9.7 million in
2000. The increase in operating expenses and loss is due to the advancement
of the Company’s drug candidates to later-stage clinical trials: MBI 226
for preventing central venous catheter-related bloodstream infections in
Phase III and MBI 594AN for treating acne in Phase II. Research and
development expenses for the twelve months increased 61 percent to $11.1
million compared with $6.9 million in 2000. Clinical development program
costs represented $7.3 million (2000: $3.5 million) or 65 percent (2000: 50
percent) of research and development expenses.
There are currently 39,374,059 common shares (April 30,
2001: 39,359,059) issued and outstanding.
The Company’s Annual General Meeting will be held on
September 6, 2001 at 2:00 pm. in the Cheakamus Room at the Waterfront Centre
Hotel, Vancouver, British Columbia. The record date is July 31, 2001.
About Micrologix
Micrologix 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 two drugs in clinical trials in the United States: MBI 226 for
preventing catheter-related bloodstream infections in Phase III and MBI
594AN for treating acne in Phase II. The Company’s common shares are
included in the TSE 300 Composite Index.
"Arthur J. Ayres"
_______________________________
Arthur J. Ayres, CA
Vice President Finance & CFO
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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 has not reviewed and does not accept
responsibility for the adequacy or accuracy of this release.
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