Orphan Medical, Inc. (Nasdaq:ORPH), Minneapolis, has announced
results for the first quarter ended March 31, 2004. Revenue for the
quarter was $5.4 million, which includes $1 million of licensing
revenue. The $4.4 million in product revenue was highlighted by growth
in Xyrem(R) (sodium oxybate) oral solution and strong Antizol(R)
(fomepizole) Injection sales. Xyrem revenue for the quarter was $1.7
million compared to $0.6 million in the prior year. Orphan Medical
reported a net loss to common shareholders of $4.3 million, or $0.40 per
share, compared to a net loss of $4.1 million, or $0.39 per share, in
the first quarter of 2003.
Compared to the first quarter of 2003, revenues from currently
marketed products increased approximately 81 percent, but overall
revenue decreased by four percent from the $4.6 million reported in the
first quarter of 2003 due to the divestment of three products in 2003.
Licensing and royalty revenue includes the milestone payment from our
European partner, Celltech Pharmaceuticals, related to the filing of the
Xyrem marketing authorization application for approval in the European
Union.
Development expenses increased to $4.2 million for the quarter
ended March 31, 2004, compared to $2.2 million in the prior year, due to
higher spending related to two ongoing clinical trials to evaluate Xyrem
as a treatment for excessive daytime sleepiness (EDS) in narcolepsy.
Sales and marketing expenses decreased to $3.4 million from $4.3 million
in the first quarter of 2003, which included Xyrem launch activities.
General and administrative expenses decreased to $1.2 million in the
quarter ended March 31, 2004, compared to $1.3 million for the same
period in 2003. The decrease from the prior year in both general and
administrative expenses and sales and marketing expenses were the result
of staff and program reductions resulting from the product divestments
in the second quarter of 2003.
As of March 31, 2004, the company had over $18 million in cash. The
company used approximately $5.2 million in cash during the first-quarter
of 2004, compared to $5.9 million used in the previous quarter. The
company projects that cash usage will decline slightly in subsequent
quarters of 2004 as a result of increasing revenue and decreasing
clinical trial activity with the completion of two EDS trials. The
company expects that its current cash position along with expected
milestone payments resulting from its licensing agreement with Celltech
will be sufficient to fund operations well into 2005.
The company also announced that it has filed an Investigational New
Drug (IND) Application to begin a clinical trial to assess Xyrem in the
treatment of fibromyalgia syndrome. The Food and Drug Administration
(FDA) has received the application and has begun its statutory review of
the IND. The company expects to initiate the trial during the second
quarter of 2004.
"Xyrem continues to make steady progress on both the
commercial and development fronts," said John Bullion, Orphan
Medical CEO. "Xyrem prescribing grew well during the first quarter,
especially in the second half of the quarter and sales of our antidote
product Antizol were very strong. We are reaffirming guidance of $18-$20
million in total 2004 revenues with Xyrem revenues contributing $12 to
$14 million. The balance of the year is going to be very exciting as the
Xyrem EDS trial results are analyzed, the fibromyalgia trial is
advanced, and we submit our supplemental NDA."
Xyrem Update
As of March 31, 2004 more than 1,400 physicians had written Xyrem
prescriptions. In the most recent six-week period, a record 744 new
prescriptions were written for Xyrem. As previously announced, there
were a total of 2,738 prescriptions filled in the last six-weeks
bringing the total to 5,087 in the first-quarter of 2004.
As previously mentioned, two Phase III(b) trials are underway to
evaluate Xyrem in the treatment of EDS in narcolepsy. The clinical
portions of the first of these trials, SXB-15, is complete.
Patient enrollment in the second EDS trial, the EXCEEDS trial, is
nearing completion and expected to be complete in the third-quarter.
Orphan Medical plans to include results from both EDS trials in a
supplemental NDA to be submitted to the FDA in late 2004.
Narcolepsy is a chronic, debilitating neurological disease.
Cataplexy associated with narcolepsy, a sudden loss of muscle tone, is
usually triggered by strong emotions such as laughter, anger, or
surprise. As such, patients often selectively isolate themselves from
interaction with others resulting in a dramatic effect on a
patient's quality of life. Narcolepsy afflicts approximately
100,000 to 140,000 Americans with about 50,000 to 75,000 patients
receiving some form of treatment for their symptoms. An estimated sixty
to ninety percent of those with narcolepsy suffer from cataplexy.
Fibromyalgia is a chronic condition that is estimated to affect as
many as four million individuals in the United States and represents a
market opportunity in excess of a billion dollars per year. The disease
is characterized by widespread muscle pain and stiffness and affects
women three times more often than men. Other symptoms include persistent
fatigue, headaches, cognitive or memory impairment, morning stiffness
and non-restorative sleep.
Orphan Medical acquires, develops, and markets pharmaceuticals of
high medical value for inadequately treated and uncommon CNS diseases
treated by specialist physicians. The lead product for the company is
Xyrem, which is the first and only approved treatment for cataplexy
associated with narcolepsy. Xyrem is also being assessed as a treatment
for the full range of narcolepsy symptoms including excessive daytime
sleepiness. Orphan Medical's pipeline includes development stage
products for fibromyalgia and pain.
For more information, visit http://www.orphan.com or call
952-513-6900.
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