XTLbio has Initiated the Phase 1a Clinical Trial of XTL-6865 for the Treatment of Hepatitis C
29 September 2005 - 6:55PM
PR Newswire (US)
REHOVOT, Israel, September 29 /PRNewswire-FirstCall/ -- XTL
Biopharmaceuticals Ltd ("XTLbio") (LSE:XTL)(NASDAQ:XTLB) today
announced that it has initiated the Phase1a clinical trial of
XTL-6865 for the treatment of hepatitis C ("HCV"). This trial is
being conducted under an investigational new drug application
("IND"), filed with the Food and Drug Administration ("FDA") in
April this year. The trial is a multi-center trial and will be
conducted in the US and Israel. XTL-6865 is being developed to
prevent HCV re-infection following a liver transplant and for the
treatment of chronic HCV disease. XTL-6865 is a combination of two
fully human monoclonal antibodies (Ab68 and Ab65) against the
hepatitis C virus E2 envelope protein. A single antibody version of
this product was tested in a pilot clinical program that included
both Phase I and Phase II clinical trials and provided preliminary
evidence of anti-viral activity in humans. Michael Weiss, XTLbio's
Chairman, commented: "Earlier this year, we set the initiation of
clinical trials with XTL-6865 as a significant corporate milestone
for 2005. We are very pleased to have accomplished this milestone,
and look forward to the further advancement of this important
product in our HCV portfolio" Contacts: XTLbio Jonathan Burgin,
Chief Financial Officer Tel: +972-8-930-4440 About XTL
Biopharmaceuticals Ltd. XTL Biopharmaceuticals Ltd. (XTLbio) is a
biopharmaceutical company developing drugs against hepatitis.
Established in 1993, XTLbio became a public company in 2000 and its
ordinary shares are listed on the Official List of the UK Listing
Authority and are traded on the London Stock Exchange under the
symbol XTL and on the Tel Aviv Stock Exchange, Israel, and ADR's,
representing 10 ordinary shares each, are traded on The NASDAQ
Stock Market under the symbol XTLB. Cautionary Statement Some of
the statements included in this press release may be
forward-looking statements that involve a number of risks and
uncertainties. For those statements, we claim the protection of the
safe harbor for forward-looking statements contained in the US
Private Securities Litigation Reform Act of 1995. Among the factors
that could cause our actual results to differ materially, and
therefore affect interest by investors in our securities, are the
following: the results of prior trails with XTL-686are not
necessarily indicative of the results we may have in the Phase 1a
and 1b trials; and other risk factors identified from time to time
in our reports filed with the various regulatory bodies. Any
forward-looking statements set forth in this press release speak
only as of the date of this press release. We do not intend to
update any of these forward-looking statements to reflect events or
circumstances that occur after the date hereof. This press release
and prior releases are available at http://www.xtlbio.com/. The
information in our website is not incorporated by reference into
this press release and is included as an inactive textual reference
only. DATASOURCE: XTL Biopharmaceuticals Ltd. CONTACT: Contacts:
XTLbio, Jonathan Burgin, Chief Financial Officer Tel:
+972-8-930-4440
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