BioTransplant Incorporated (Nasdaq: BTRN), Charlestown, Mass., has
reported financial results for the second quarter and six- month period
ended June 30, 2002.
For the quarter ended June 30, 2002, the company reported a net
loss of $24.08 million, or $1.08 per share, compared to a net loss of
$25.56 million, or $1.76 per share, for the same period in 2001.
Weighted average shares outstanding for the quarters ended June 30, 2002
and 2001 were approximately 22.21 million and 14.50 million,
respectively.
The net loss for the second quarter of 2002 includes a loss from
impairment of $17.96 million related to the goodwill and intangible
assets acquired by BioTransplant in its acquisition of Eligix, Inc. in
2001. Management has concluded that these non-cash assets incurred a
decrease in value because sales of the Eligix(TM) HDM Cell Separation
Systems have been significantly below expectations and because the
company has recently undergone two reductions in force.
"This impairment charge represents an adjustment to the
goodwill and intangible assets associated with the Eligix(TM)
acquisition," commented Donald B. Hawthorne, president and CEO of
BioTransplant. "We believe both cash expenses, as reduced on July
29, and these non-cash assets, as reduced by this charge, are now
consistent with current product revenue expectations."
Revenues for the second quarter of 2002 totaled $0.39 million,
compared to $0 in revenue reported the same quarter last year. The
increase in revenues was due to two factors. First, the company
recognized $0.18 million in product revenue from sales of the Eligix(TM)
HDM Cell Separation Systems, which were launched in Europe during the
fourth quarter of 2001 by the company's distribution partner,
Gambro BCT. Second, $0.22 million in license and milestone revenue was
recognized in the second quarter 2002 as the $6.0 million of upfront
fees and milestone payments received under the Gambro exclusive
distribution agreement are being recognized as revenue ratably over the
life of the agreement.
Research and development expenses for the three months ended June
30, 2002 were $4.36 million, compared to $2.91 million for the
comparable period of 2001. Sales, general and administrative expenses
for the three months ended June 30, 2002 were $1.06 million, compared to
$0.88 million for the comparable period of 2001.
The company had cash, cash equivalents and short-term investments
of $13.24 million as of June 30, 2002, as compared to $9.79 million as
of March 31, 2002.
Financial Guidance
The company expects that total revenues for the fiscal year ending
December 31, 2002 will be approximately $1.50-1.60 million, of which
Eligix(TM) product revenues are expected to be between $0.70-0.80
million. Eligix(TM) product revenues of approximately $0.30 million are
expected in the second half of 2002.
The company estimates that existing cash resources will last into
the third quarter of 2003. The receipt of potential milestone payments
could make cash resources last until fourth quarter 2003; however, there
can be no assurance as to whether or when the company will receive these
potential milestone payments.
Recent Highlights
Appointment of New CEO
Donald B. Hawthorne was appointed by the board of directors to the
position of president and CEO of the company on July 19. Hawthorne
brings 19 years of leadership experience in the healthcare industry to
the company. He succeeds Elliot Lebowitz, the company's founding
CEO, who will serve as chairman of the board until September 11 and
remain as a Board member thereafter.
New Strategic Focus and Restructuring Plan
The company announced a restructuring plan on July 29 intended to
streamline the company's operations around a new strategic focus.
The plan includes the following initiatives:
- Accelerating Eligix(TM) Product Sales: BioTransplant sales
people, technical support, and clinical support personnel will spend a
substantial amount of time working in Europe to enhance Gambro's
sales effort.
- Revamped AlloMune System Development Strategy: The company
revised its clinical development strategy for the AlloMune System and
will now employ kits consisting of BioTransplant's proprietary
antibody MEDI-507, also known as siplizumab, in combination with
products that have already been approved in the United States.
- Reduced Cash Burn Rate: The company implemented a reduction in
headcount of approximately 23%, which is expected to lower the cash burn
rate by approximately 25%.
The company also announced that the restructuring would not affect
its agreement with MedImmune or MedImmune's development efforts for
MEDI-507.
Common Stock Offering Yielding $9.7 Million in Net Proceeds to
company. In June, BioTransplant completed an offering of 4 million
shares of its common stock at a price of $2.50 per share.
Approval Granted to Market the Eligix(TM) CD8-SC Cell Separation
System in Europe. BioTransplant announced on July 26 that it had
received approval to market its third HDM Cell Separation System product
in the European Union. The Eligix(TM) CD8-SC Cell Separation System is
intended for ex-vivo use for patients receiving allogeneic bone marrow
and peripheral stem cell transplantation for hematological disorders.
About BioTransplant
BioTransplant Incorporated, headquartered in Charlestown,
Massachusetts, is developing a portfolio of products for application in
a range of medical conditions, including treatment of cancer and
autoimmune diseases, organ and tissue transplantation, for which current
therapies are inadequate. Siplizumab (MEDI-507), a lead product the
company exclusively licensed to MedImmune, is in Phase II clinical
trials for the treatment of psoriasis. In addition, the company is
developing the AlloMune System, which is designed to treat a variety of
hematologic malignancies, and its distribution partner Gambro BCT
markets the Eligix(TM) family of cell separation products in Europe for
use in bone marrow, stem cell and donor leukocyte transplants.
For more information, call 617/241-5200 or visit
http://www.biotransplant.com.
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