Benitec Raises AU$8 million to Forge Ahead with its Gene Silencing Therapeutics: Rights Issue Closes Oversubscribed
17 May 2011 - 10:29PM
Business Wire
Benitec Ltd (ASX:BLT), a world leader in RNA-based gene
silencing for human therapeutics, today announced its fully
underwritten AU$8 million renounceable rights issue, incorporating
an entitlement offer and a shortfall offer, had successfully closed
oversubscribed.
The offer was 4 new shares for every 5 fully paid ordinary
shares held plus 1 new free listed option for every 4 new shares
issued, resulting in the issue of 404,565,897 new shares and
101,141,474 new listed options with an exercise price of AU$0.04 (4
cents) and an expiry date of 31 December 2013. A further
100,160,982 options, with the same terms as above, will be issued
to the sub-underwriters of the issue.
Benitec has received rights issue acceptances for 302,716,126
shares, with the shortfall applications from existing shareholders
causing the remainder of the issue to be oversubscribed.
“The positive investor and shareholder response reflects the
major strides forward Benitec has made this year and is an
overwhelming vote of confidence in Benitec’s management and
strategy by its shareholders. Demand for Benitec stock through the
rights issue has been exceptionally strong – resulting in demand
outstripping supply. Not only was there a very high proportion of
entitlements taken up, but a significant percentage of shareholders
applied for shares in excess of their entitlement,” said Mr Peter
Francis, Benitec’s Chairman.
Dr Peter French, Benitec's CEO, added “Together with the
favourable ruling by the US Patent and Trademark Office late last
year, and other favourable decisions since including in Europe,
this enables the relaunch of Benitec. We are now able to actively
pursue a number of programs and corporate initiatives to progress
our transformational gene silencing technology and drive the value
of the Company.”
The net proceeds from the issue will enable the Company to
proceed with further research and development of its existing
projects, based on its DNA-directed RNA interference (ddRNAi)
technology including advancing its Chronic Cancer-Associated Pain
Program and Drug-Resistant Lung Cancer Program to Phase I/II and
progressing the Hepatitis B Program to completion of preclinical
and toxicology studies. Funds will also be utilised to pursue new
opportunities in the licensing and collaboration of the Company’s
patent estate and the termination of the funding arrangement with
La Jolla Cove Investors Inc.
The Board would like to sincerely thank all shareholders who
participated in the rights issue. We are also pleased to
have had the support of Patersons Securities Ltd as Lead Manager
and Underwriter to the offer.
--ends--
About Benitec www.benitec.com
Benitec Limited is developing new novel treatments for chronic
and life-threatening conditions based on a transformational
technology, DNA-directed RNA interference (ddRNAi) - sometimes
called expressed RNAi. The technology’s potential to address unmet
medical needs and, potentially, to cure disease results from its
demonstrated ability to permanently silence genes which cause the
condition.
Benitec now either owns or exclusively licences from CSIRO more
than 40 granted or allowed patents in the field of RNA interference
for human therapeutic applications. Patents have been granted in
key territories such as the USA, the UK, Japan, Europe, Canada and
Australia. In addition, Benitec has almost 50 patent applications
pending for which it is the owner or exclusive licensee from CSIRO,
and has further intellectual property under development as a result
of its pipeline program.
Benitec trades on the Australian stock exchange under the symbol
“BLT”. The Company was founded in 1997 and has been publicly held
since 2001. The Company aims to deliver a range of novel
ddRNAi-based therapeutics to the clinic in partnership with the
pharmaceutical industry. In-house it is pursuing a focused R&D
strategy in infectious diseases, cancer and chronic
cancer-associated pain, as well as programs with licensees that
have advanced to pre-clinical and/or clinical trials.
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