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METABASIS ANNOUNCES SECOND QUARTER 2004 FINANCIAL RESULTS
SAN DIEGO, CA - August 12, 2004 - Metabasis Therapeutics,
Inc. (NASDAQ: MBRX) today reported financial results for the three
months and six months ended June 30, 2004.
Financial Review
On June 21, 2004, Metabasis completed an initial public offering
in which the company sold 5,000,000 shares of common stock for proceeds
of $30.7 million, net of underwriting discounts and commissions
and offering expenses. As of June 30, 2004, Metabasis had $51.4
million in cash and cash equivalents and short-term investments
available-for-sale as compared to $25.3 million as of December 31,
2003, an increase of $26.1 million. The increase was mainly due
to the issuance of common stock in connection with our initial public
offering in June 2004.
Revenues for the three months and six months ended June 30, 2004
were $1.8 million and $5.9 million, respectively, compared to $2.0
million and $3.0 million for the same periods in 2003. The net loss
for the three months ended June 30, 2004 was $3.6 million, or $1.17
per share, compared to a net loss of $2.3 million, or $1.42 per
share, in the second quarter of 2003. The net loss for the six months
ended June 30, 2004 was $4.1 million, or $1.85 per share, compared
to a net loss of $5.7 million, or $3.60 per share, for the same
period in 2003. The increase in year-to-date revenues and corresponding
decreases both in year-to-date net loss and net loss per share were
attributable primarily to payments received by the company from
its partners for the successful attainment of clinical development
milestones. These revenue increases were partially offset by increases
in year-to-date research and development and general and administrative
expenses associated with the company's growth, the advancement of
its product pipeline and its transition to a public company.
"While our year-to-date net loss and net loss per share were
positively impacted by the milestone payments we received from our
partners, we expect net loss and net loss per share to fluctuate
from quarter to quarter as the company continues to grow and pursue
its clinical objectives," said John Beck, Metabasis' Vice President
of Finance and CFO.
Dr. Paul Laikind, Chairman, President and CEO said, "The second
quarter was very productive for Metabasis with excellent progress
made on our strategic goals. We made important advances with the
three product candidates we have in the clinic, including successful
completion of proof of concept studies on CS-917, our first generation
gluconeogenesis inhibitor for diabetes and on remofovir, our HepDirect
antiviral for the treatment of hepatitis B. Our third clinical stage
product candidate, MB07133, for the treatment of primary liver cancer,
is also progressing well with the current study in patients expected
to be completed around year-end."
Dr. Laikind further stated, "The Company also made excellent
progress on its efforts to further bolster its product pipeline
through internal discovery. We expect to file an IND on MB07803,
a 2nd generation gluconeogenesis inhibitor for the treatment of
diabetes, around the end of the year and we have other advanced
research programs that could yield additional clinical development
candidates over the next twelve to twenty-four months for the treatment
of diseases such as hyperlipidemia, diabetes and possibly obesity.
We are also making progress in our hepatitis C collaboration with
Merck. Of course, a key event for the company was the completion
of our initial public offering in June. The resources provided by
the IPO position us well to strategically pursue our corporate objectives."
Recent Highlights
- CS-917: Reported Preliminary Evidence of Efficacy and Earned
a Milestone: Completed a Phase 2, proof of concept study of
CS-917 in patients with type 2 diabetes mellitus that provided
preliminary evidence of efficacy. Earned a $3.5 million milestone
payment from its partner on the project, Sankyo Co., Ltd.
- Remofovir: Reported Preliminary Evidence of Efficacy and
Earned a Milestone: Data from the first three of four doses
in a 28-day study in patients infected with the hepatitis B virus
provided the first preliminary evidence of efficacy. The results
were consistent with expected results for Metabasis' HepDirectTM
technology based on previous pre-clinical studies. A decision
was made by the company's partner and licensee for the product,
Valeant Pharmaceuticals International, to proceed with development
and Metabasis earned a $1 million milestone payment.
- Remofovir: Initiated a Phase 2, Multi-center Clinical Study:
Valeant is enrolling patients in the U.S. and Asia and results
from this trial would be used for selection of the dose for Phase
3 studies that would be expected to begin in 2005 if all goes
according to plan.
- Completed Initial Public Offering (IPO): Metabasis issued
5 million shares at $7.00 a share garnering gross proceeds of
$35 million in June 2004.
- Published a Key Report on the HepDirect Technology: Metabasis
scientists published an article in the prestigious peer-reviewed
Journal of the American Chemical Society (JACS) describing aspects
of the company's proprietary HepDirect prodrug technology that
the company uses to direct drugs to the liver to treat metabolic
and liver diseases. Subsequent to the article appearing in JACS,
Nature published a brief review highlighting the technology in
its "News and Views" section.
- Issuance of Four Patents Bolstered Proprietary Position
on Products and Technology: New patents issued, including
an important patent related to the HepDirect prodrug technology
and the gluconeogenesis inhibitor program that expand and strengthen
the company's proprietary position.
Conference Call
Metabasis management team will host a conference call and live
webcast today to discuss second quarter 2004 financial results at
4:30 p.m. Eastern Time (1:30 p.m. Pacific Time). Individuals interested
in participating in the call may do so by dialing (800) 299-9630
for domestic callers and (617) 786-2904 for international callers.
Please specify to the operator that you would like to join the "Metabasis
Second Quarter Financial Results Conference Call." The conference
call will be webcast live on Metabasis' website at http://www.mbasis.com
under the "Investor" section, and will be archived there
for 30 days following the call. Please connect to Metabasis' website
several minutes prior to the start of the conference call to ensure
adequate time for any software download that may be necessary.
About Metabasis (www.mbasis.com):
Metabasis Therapeutics, Inc. is a biopharmaceutical company focused
on the discovery, development and commercialization of novel small
molecule drugs principally to treat metabolic diseases linked to
pathways in the liver and to treat liver diseases. The company has
established a broad product pipeline targeting large markets with
significant unmet medical needs. Metabasis has three internally
discovered, novel product candidates in clinical development: CS-917,
remofovir and MB07133, indicated for the treatment of type 2 diabetes,
hepatitis B and primary liver cancer, respectively. All three products
are being studied in patients and preliminary evidence of efficacy
has been demonstrated with CS-917 and remofovir. Metabasis has developed
several proprietary technologies for use in discovering and optimizing
drugs, including the NuMimetic technology and the HepDirect
technology. The NuMimetic technology was used to discover CS-917,
a first-in-class gluconeogenesis inhibitor, and was also used to
identify MB07803, a 2nd generation gluconeogenesis inhibitor that
is expected to enter the clinic in 2005 for the treatment of type
2 diabetes. The HepDirect technology, a liver-targeting prodrug
technology, was used to develop remofovir and MB07133 and is also
being used in a partnership with Merck to discover new treatments
for hepatitis C. Metabasis is continuing to identify and develop
new product candidates using its proprietary technologies and know-how.
Forward-Looking Statements:
Statements in this press release that are not strictly historical
in nature constitute "forward-looking statements." Such
statements include, but are not limited to, references to Metabasis'
progress on its strategic goals and pursuit of its corporate objectives,
the completion of clinical trials for Metabasis' product candidates,
the expansion of Metabasis' product pipeline including the filing
of an IND for MB07803 and the designation of additional product
candidates from Metabasis' advanced research programs, and the strength
of Metabasis' proprietary position as well as other statements about
Metabasis' proprietary technologies, product candidates, research
programs and collaborations. Such forward-looking statements involve
known and unknown risks, uncertainties and other factors which may
cause Metabasis' actual results to be materially different from
historical results or from any results expressed or implied by such
forward-looking statements. These factors include, but are not limited
to, risks and uncertainties related to the progress and timing of
clinical trials for Metabasis' product candidates; the fact that
positive results from pre-clinical studies and early clinical trials
does not necessarily mean later clinical trials will succeed; difficulties
or delays in development, testing, obtaining regulatory approval,
producing and marketing Metabasis' product candidates; adverse side
effects or inadequate efficacy of Metabasis' product candidates
or proprietary technologies; Metabasis' dependence on its licensees
and collaborators for the clinical development and registration
of its product candidates, among other things; the scope and validity
of intellectual property protection for Metabasis' product candidates,
proprietary technologies and their uses; competition from other
pharmaceutical or biotechnology companies; Metabasis' ability to
obtain additional financing to support its operations; and other
factors discussed in the "Risk Factors" section of Metabasis'
prospectus filed with the Securities and Exchange Commission pursuant
to Rule 424(b)(4) of the Securities Act on June 16, 2004. All forward-looking
statements are qualified in their entirety by this cautionary statement.
Metabasis is providing this information as of this date of this
release and does not undertake any obligation to update any forward-looking
statements contained in this release as a result of new information,
future events or otherwise.

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