Research Update: SMT C1100 Receives Orphan Drug Status from the US FDA for the Treatment of DMD
24 November 2011 - 6:00PM
UK Regulatory
TIDMSUMM
Summit Corporation plc
('Summit' or 'the Company')
SMT C1100 RECEIVES ORPHAN DRUG STATUS FROM THE US FDA FOR THE TREATMENT OF
DUCHENNE MUSCULAR DYSTROPHY
Oxford, UK, 24 November 2011, Summit (AIM: SUMM), a UK drug discovery company,
is pleased to announce that the United States Food & Drug Administration ('the
US FDA') has granted orphan drug status to the clinical candidate SMT C1100 for
the treatment of Duchenne Muscular Dystrophy ('DMD'), a fatal genetic
neuromuscular disorder for which there is currently no cure. The European
Medicines Agency had granted SMT C1100 orphan drug status in December 2008.
Commenting on the news, Barry Price, PhD, Executive Chairman of Summit said:
"We are pleased the US FDA has designated SMT C1100 as an orphan drug for DMD as
this recognises its potential to treat a major unmet medical need. Our clinical
candidate has now been granted orphan drug status both in Europe and the US, and
this status will provide additional regulatory support and various commercial
benefits including extended periods of market exclusivity.
"Summit believes that SMT C1100 can become a first-in-class treatment for DMD
and it is our intention to commence a clinical study that will evaluate a new
formulation of this drug that will benefit all patients with this fatal
disease."
About Orphan Drug Designation
An orphan drug is a pharmaceutical agent that has been developed specifically to
treat a rare medical condition, the condition itself being referred to as an
orphan disease. The US Orphan Drug Act and European Orphan legislation are
designed to assist and encourage companies in the development of urgently needed
drugs for the treatment of rare diseases. Orphan drug designation has a number
of benefits including a valuable seven-year period of market exclusivity in the
US following approval. In Europe, a ten-year period of exclusivity is provided.
Orphan products can also expect to receive additional regulatory support,
reduced fees and accelerated approval. Further information about orphan drug
designation can be found on the FDA's website,www.fda.com/oprhan.
About DMD and SMT C1100
DMD is caused by the absence of a protein called dystrophin which results in the
degeneration of all skeletal and other vital muscles such as the heart. There
is no cure for DMD with the only available treatments being steroids that
provide symptomatic relief.
SMT C1100 is a small molecule drug that works by increasing (upregulating)
production of a similar, naturally occurring protein called utrophin to replace
the missing dystrophin. Summit recently published compelling preclinical data
showing SMT C1100 can increase utrophin production to restore and maintain
healthy muscle function. A major advantage of utrophin upregulation is it will
benefit all patients with DMD regardless of their specific genetic mutation and
is expected to be complementary with other therapeutic approaches currently in
development.
- END -
For more information, please contact:
Summit
Barry Price, PhD,
Richard Pye, PhD Tel: +44 (0)1235 443 951
Singer Capital Markets
(Nominated Adviser and Joint broker)
Shaun Dobson / Claes Spång Tel: +44 (0)203 205 7500
Hybridan LLP
(Joint broker)
Claire Louise Noyce Tel: +44 (0)207 947 4004
Peckwater PR
(Financial public relations) Tel: +44 (0)7879 458 364
Tarquin Edwards tarquin.edwards@peckwaterpr.co.uk
Notes to Editors
About Summit
Summit is an Oxford, UK based drug discovery company with an innovative
technology platform called Seglins for the discovery of new medicines, a
portfolio of drug programme assets and a commercial strategy of signing multiple
early-stage deals.
Seglin(TM) technology is using new chemistry to access biological drug targets
that cannot be exploited by conventional drug discovery approaches. Summit's
internal research is currently focussed in high-value therapy areas and the
Company will further exploit the technology's wider potential through strategic
alliances. Summit's programme portfolio consists of a number of drug programmes
targeting high-value areas of unmet medical need including Duchenne Muscular
Dystrophy and C. difficile infection.
Summit's commercial strategy focuses on signing multiple early-stage drug
programme and technology platform deals that generate upfront cash, transfer
development costs from the Company, and retain valuable upside potential.
Summit is listed on the AIM market of the London Stock Exchange and trades under
the ticker symbol SUMM. Further information is available atwww.summitplc.com.
Forward Looking Statements
This document contains "forward-looking statements" within the meaning of the
U.S. Private Securities Litigation Reform Act of 1995. Forward-looking
statements can be identified by words such as "anticipates", "intends", "plans",
"seeks", "believes", "estimates", "expects" and similar references to future
periods, or by the inclusion of forecasts or projections. Forward-looking
statements are based on the Company's current expectations and assumptions
regarding our business, the economy and other future conditions. Because
forward-looking statements relate to the future, by their nature, they are
subject to inherent uncertainties, risks and changes in circumstances that are
difficult to predict. The Company's actual results may differ materially from
those contemplated by the forward-looking statements. The Company cautions you
therefore that you should not rely on any of these forward-looking statements as
statements of historical fact or as guarantees or assurances of future
performance. Important factors that could cause actual results to differ
materially from those in the forward-looking statements and regional, national,
global political, economic, business, competitive, market and regulatory
conditions.
This announcement is distributed by Thomson Reuters on behalf of
Thomson Reuters clients. The owner of this announcement warrants that:
(i) the releases contained herein are protected by copyright and
other applicable laws; and
(ii) they are solely responsible for the content, accuracy and
originality of the information contained therein.
Source: Summit Corporation PLC via Thomson Reuters ONE
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