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Varisolve NDA submitted to the FDA

4 Feb 2013 07:00

RNS Number : 9947W
BTG PLC
04 February 2013
 



BTG plc: Varisolve® NDA submitted to the FDA

 

London, UK, 4 February 2013: BTG plc (LSE: BTG), the specialist healthcare company, today announces that a New Drug Application (NDA) seeking approval of Varisolve® (polidocanol endovenous microfoam (PEM)) as a comprehensive treatment for varicose veins has been submitted to the US Food & Drug Administration (FDA). BTG expects to hear within Q2 2013 (calendar year) as per the usual FDA timelines whether after initial review the submission has been accepted for full review.

 

For further information contact:

 

BTG

FTI Consulting

Andy Burrows, Director of Investor Relations

+44 (0)20 7575 1741; Mobile: +44 (0)7990 530605

 

Rolf Soderstrom, Chief Financial Officer

+44 (0)20 7575 0000

Ben Atwell

+44 (0)20 7831 3113

 

 

About BTG

BTG is an international specialist healthcare company that is developing and commercialising products targeting critical care, cancer and other disorders. The Group is seeking to acquire new products to develop and market to specialist physicians, and is building a sustainable business financed by revenues from sales of its own marketed products and from royalties and milestone payments on partnered products.For further information about BTG please visit our website at www.btgplc.com.

This information is provided by RNS
The company news service from the London Stock Exchange
 
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