Hexvix
hexaminolevulinate
Treatment for Detection of Bladder CancerFDA Requests More Information Related to Hexvix NDA
OSLO, Norway, April 20, 2006 - PhotoCure ASA has received a
non-approvable letter from the United States Food and Drug
Administration (FDA) related to the Hexvix new drug application
(NDA). FDA has requested additional analyses and information.
PhotoCure will, together with its US regulatory advisors, initiate
a discussion with FDA to better understand the additional
requirements necessary to obtain approval for Hexvix from the
agency. This discussion will take place over the coming
months.
PhotoCure is currently conducting a multicenter phase III clinical
study for Hexvix in the EU/US. This study is not part of the
initial application and may provide useful supplementary clinical
data. This study is scheduled to be concluded in 2007.
Dr. Kjetil Hestdal, President and CEO of PhotoCure, comments: "We
are disappointed with this initial decision by the FDA. However, we
will continue our constructive dialogue with the agency with the
aim to agree upon the actions that must be taken to address the
deficiencies identified by the FDA."
Hexvix has previously been approved for the detection of bladder
cancer in patients with known or suspected bladder cancer in 27
European countries.
Bladder cancer is the third most common malignant disease
worldwide, with approximately four million cystoscopies performed
in the USA and Europe every year. Patients have a good prognosis if
diagnosed early and treated adequately. Hexvix Imaging is an
innovative and effective diagnostic method that can be used for all
types of bladder cancer, and will be used as a supplement to
current standard methods. It is in particular effective for
carcinoma in situ (CIS), a highly malignant cancer that is
difficult to see with standard white light cystoscopy. Hexvix gives
a more accurate diagnosis than current standard methods and will
therefore provide health economic benefits.
PhotoCure ASA is a Norwegian pharmaceutical company founded in 1993
and listed on Oslo Stock Exchange. The company develops and sells
pharmaceuticals and medical devices based on proprietary
photodynamic technologies, targeting key dermatology and oncology
markets.
PhotoCure has two products with sales and marketing approvals:
Metvix, which is a product developed for the treatment of skin
cancer (basal cell carcinoma) and pre-cancerous skin lesions
(actinic keratosis), and Hexvix, which is developed for the
detection of bladder cancer. Both products are based on the same
photodynamic technology, combining the drug known as a
photosensitiser with a light source that activates the
photosensitiser. PhotoCure is currently testing both products for
new indications and aims to develop a pipeline of follow-on
products and technologies.
Click here for more information on Hexvix from the manufacturer.
New Drug Applications Archive
2007: Jan | Feb | Mar | Apr | May | Jun | Jul | Aug | Sep | Oct | Nov | Dec
2006: Jan | Feb | Mar | Apr | May | Jun | Jul | Aug | Sep | Oct | Nov | Dec
2005: Jan | Feb | Mar | Apr | May | Jun | Jul | Aug | Sep | Oct | Nov | Dec
2004: Jan | Feb | Mar | Apr | May | Jun | Jul | Aug | Sep | Oct | Nov | Dec





