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Company Announcement
Dr Aston appointed to Biological Committee of Government IR&D Board
Melbourne, Australia July 10th, 2007 Clinuvel Pharmaceuticals Limited (ASX: CUV, Germany-XETRA:UR9)
is pleased to announce that Dr Roger Aston, Clinuvel’s Executive Chairman has been appointed as a member
of the Biological Committee of the Industry Research and Development Board. Dr Aston was appointed to the
Board by The Hon Ian Macfarlane, Australia’s Minister for Industry, Tourism and Resources.
The Board was established on 1 July 1986, under the Industry Research and Development Act 1986. Its
mission is to increase the economic return from successful technology-based enterprises in Australia by guiding
the Australian Government's investment in the commercialisation of the nation's research and development and
innovation. The Biological Committee assesses Commercial Ready applications, and variations to R&DStart
and BIF grants, and makes recommendations for grant funding involving products, processes or services in the
following industries: health, medical sciences, agriculture, fishing, forestry, environmental, food-processing.
(Source: www.ausindustry.gov.au)
About Clinuvel Pharmaceuticals Limited
Clinuvel Pharmaceuticals Limited (ASX:CUV, XETRA/DAX:UR9, ADR:CUVLY) is an Australian
biopharmaceutical company developing its photo-protective drug CUV1647 as a preventative treatment for a
range of UV-related skin disorders as well as in cancer related treatments.
The five indications are:
Indication Description Clinical Trial Status
Polymorphic Light Eruption
(PLE / PMLE)
Sun poisoning Phase III trials began May 2007
Erythropoietic Protoporphyria (EPP) Absolute sun intolerance Phase III trials began June 2007
Squamous Cell Carcinoma (SCC)
and Actinic Keratosis (AK) in organ
transplant patients
Non-melanoma skin
cancers / precursor
to skin cancers
Phase II trials planned to
begin 2007
Solar Urticaria (SU) Acute anaphylactic
reaction to sun
Phase II trials planned to
begin 2007
Phototoxicity associated with
Photodynamic Therapy (PDT)
Photo-sensitivity associated
with cancer treatment
Phase II trials planned to
begin 2007
Phase I and II human clinical trials using CUV1647 have demonstrated that the drug is well tolerated and no
significant safety concerns have been identified to date.
Following successful conclusion of the development program, Clinuvel will work closely with global regulators to
facilitate marketing approval of CUV1647.
-END
 
aus der Diskussion: CLINUVEL PHARMACEUTICALS LTD
Autor (Datum des Eintrages): derneureiche  (10.07.07 09:53:38)
Beitrag: 57 von 22,251 (ID:30608783)
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