SI
SI
discoversearch

We've detected that you're using an ad content blocking browser plug-in or feature. Ads provide a critical source of revenue to the continued operation of Silicon Investor.  We ask that you disable ad blocking while on Silicon Investor in the best interests of our community.  If you are not using an ad blocker but are still receiving this message, make sure your browser's tracking protection is set to the 'standard' level.
Biotech / Medical : QLT PhotoTherapeutics (QLTI) -- Ignore unavailable to you. Want to Upgrade?


To: Scripts who wrote (1127)12/14/2000 8:25:11 AM
From: Al Collard  Read Replies (1) | Respond to of 1321
 
QLT issues financial update on sales outlook for Q4 2000

VANCOUVER, Dec. 14 /CNW/ - QLT (NASDAQ: QLTI, TSE: QLT) announced today
that fourth quarter demand for Visudyne(TM) vials is expected to grow 20 to
25% over Q3 which will translate into sales of approximately US$36-38 million.
Slower than expected growth is due to lack of reimbursement in some countries
in Europe and in the U.S., as well as a reduction in revenue caused by the
decline in the EURO and Swiss currencies have impacted the upside sales
potential for the current year.
"We continue to be on track for the most successful launch of an
ophthalmic product ever and will meet our original forecasts established
earlier in the year," commented Julia Levy, President and CEO of QLT.
"Unfortunately, expectations after such a strong second quarter may have been
a little too bullish given that we did not have a clear resolution on
reimbursement. We consider these issues to be short lived and are not changing
our outlook on the opportunity we have with Visudyne."
Negotiations in Europe for reimbursement continue on a country-by-country
basis between CIBA Vision, the eye care unit of Novartis AG (NYSE:NVS),
physician representatives from ophthalmology associations, and local and
government payers to ensure that third-party payers provide adequate coverage
for Visudyne therapy so that patients in Europe have access to the treatment.
Last month, in the United States, the Health Care Financing
Administration (HCFA) issued its national coverage policy for Visudyne. In
addition, the administration announced the establishment of a new procedure
code for Ocular Photodynamic Therapy along with payment levels that will take
effect on January 1, 2001.
"The National Coverage policy proposed by HCFA is a very positive step
moving forward," states Levy. "Despite the obstacles that our corporate
partner has faced both with reimbursement related issues in Europe and in the
U.S., we've seen tremendous underlying demand for Visudyne by patients and
retina specialists. To put this in perspective, we will be missing our upside
sales target by approximately 2.3% of the vials we projected we would sell,
the remainder of the sales shortfall is due to currency fluctuations."
QLT expects 2001 sales in the range of US$240-260 million.
Visudyne therapy is being co-developed for various ocular conditions by
CIBA Vision, the eye care unit of Novartis, and QLT Inc. CIBA Vision markets
the product worldwide while QLT is responsible for manufacturing. Visudyne
therapy is protected by a series of U.S. and foreign-issued patents on
composition of matter, formulations and manufacturing, and the method of use
in treating AMD and other conditions.
QLT Inc. is a world leader in the development and commercialization of
proprietary pharmaceutical products for use in photodynamic therapy, a new
field of medicine utilizing light-activated drugs in the treatment of disease.
QLT's innovative science has advanced photodynamic therapy beyond applications
in various cancers towards breakthrough treatments in ophthalmology and immune
disorders. For more information, you are invited to visit QLT's web site at
www.qltinc.com.

Visudyne(TM) is a trademark of Novartis AG

QLT Inc. is listed on The Nasdaq Stock Market under the trading symbol
"QLTI" and on The Toronto Stock Exchange under the trading symbol "QLT."

The foregoing information may contain forward-looking statements which
involve known and unknown risks, uncertainties and other factors which may
cause the actual results to be materially different from any future results,
performance or achievements expressed or implied by such statements. Such
factors include, but are not limited to: risks associated with the
commercialization of Visudyne(TM) therapy including patient and doctor demand
for the treatment; dependence on corporate relationships; manufacturing
uncertainties; uncertainty of pricing and reimbursement; uncertainties
relating to clinical trials and product development; QLT Inc.'s history of
operating losses and uncertainty of future profitability; competition; QLT
Inc.'s rapid growth; uncertainty regarding patents and proprietary rights; QLT
Inc.'s product liability claims and insurance; no assurance of regulatory
approval; government regulation; QLT Inc.'s uncertainty of access to capital;
anti-takeover provisions; and volatility of common share price; among others,
all as described in the Company's Annual Information Form on Form 10-K, and
and other filings with the U.S. Securities and Exchange Commission.