GlaxoSmithKline plc (GSK) today announces that
it has received approval from the Swedish regulatory authority (MPA) for
dutasteride, a new treatment for benign prostatic hyperplasia (BPH). The MPA
have approved an indication for its use in the treatment of moderate to severe
symptoms of BPH and for the prevention of acute urinary retention (AUR) and
surgery in patients with BPH. They have agreed to act as the Reference Member
State for the Mutual Recognition procedure within Europe and GSK plan to market
the drug in all major European markets once approvals are finalised.
Commenting on the approval, Dr Ray Dawson, Senior Director of Urology,
European Clinical Development group at GSK said: "This is good news as it
provides both patients and prescribers with a new treatment alternative.
Clinical trials for dutasteride, involving over 4,300 patients suffering from
BPH, have demonstrated that it provides long lasting symptom relief and
positively impacts on BPH progression. For instance, reductions over placebo in
prostate volume were seen as early as one month and continued through the
duration of the studies, which resulted in significantly reduced incidence of
acute urinary retention and BPH related surgery. Both of these are key
complications of BPH progression."
Dutasteride is the first 5-alpha reductase inhibitor (5ARI) that inhibits
both the type 1 and 2 isoenzymes of 5AR. These enzymes are responsible for
converting testosterone to dihydrotestosterone (DHT) in the prostate and other
tissues, and DHT has been proven to play a key role in the development and
progression of BPH.
BPH is a common benign growth in ageing men. It is this non-cancerous
enlargement of the prostate gland that frequently causes lower urinary tract
symptoms (LUTS). It is a progressive disease and if left untreated for a long
duration this condition can give rise to a reduction in quality of life and
result in complications such as AUR and surgery requiring hospitalisation.
Overall, in clinical trials, dutasteride was well tolerated and the most
commonly reported adverse events as reported in the approved Summary of Product
Characteristics were: Impotence (6%), altered / decreased libido (3.7%),
ejaculation disorder (1.8%), gynaecomastia (1.3%).
Notes to the Editors:
An original NDA, with 1-year data for
dutasteride in the treatment of symptomatic BPH, was approved by the FDA in
November 2001. A supplemental NDA with 2-year treatment data for dutasteride was
filed with the FDA in December 2001 and the product will be launched in the US
upon approval of the sNDA.
Current world-wide sales of treatments for BPH are £1,658 million.
It is estimated that over 17 million European men suffer from BPH.
Several factors are expected to contribute to an increased usage of 5ARIs
including the growing number of patients suffering from BPH due to an ageing
population, increased awareness of the condition and the trend towards
preventing long term complications.
About GSK:
GlaxoSmithKline - one of the world's leading
research-based pharmaceutical and healthcare companies - is committed to
improving the quality of human life by enabling people to do more, feel better
and live longer.
Under the safe harbor provisions of the US Private Securities Litigation
Reform Act of 1995, GlaxoSmithKline cautions investors that any forward-looking
statements or projections made by GSK, including those made in this news
release, are subject to risks and uncertainties that may cause actual results to
differ materially from those projected. Factors that may affect the company's
operations are discussed in the section "Cautionary factors that may affect
future results" in GSK's results announcement for the year ended 31 December
2001, filed with the U.S. Securities and Exchange Commission.
GSK Enquiries
| UK Media |
US Media |
Martin Sutton
Alan Chandler
Siobh?n Lavelle |
Nancy Pekarek
Mary Anne Rhyne
Patty Seif |
020 8047 5502
020 8047 5502
020 8047 5502 |
(215) 751 4232
(919) 483 2310
(215) 751 4390 |
| European Analyst/Investor |
US Analyst/Investor |
Duncan Learmouth
Philip Thomson
Joan Toohill |
Frank Murdolo
Tom Curry |
020 8047 5540
020 8047 5543
020 8047 5542 |
(215) 751 7002
(215) 751 5419 |
Updated July 25, 2002 - © 2001-2002 GlaxoSmithKline - All Rights
Reserved
Legal Notices - Privacy Statement |
|