TORONTO--(Marketwire - Aug 8, 2012) - Cynapsus Therapeutics Inc. (CTH: TSX-V) today
announced that
it has been awarded a grant of USD$947,925 from The Michael J. Fox
Foundation
for Parkinson's Research (MJFF) to support clinical studies to develop
APL-130277, a sublingual (oral) thin film strip reformulation of
apomorphine.
Apomorphine is an approved drug in the US, Europe and several other
countries as
a subcutaneous injection or infusion for Parkinson's patients experiencing
daily
"OFF" or motor fluctuation episodes. APL-130277 is potentially the only
oral
formulation of Apomorphine, and as such will provide patients with a
convenient
and more tolerable alternative to multiple daily injections.
The grant was awarded under the Foundation's The Edmond J. Safra Core
Programs
for Parkinson's Research, Clinical Intervention Award, aimed at supporting
human
clinical trials testing promising Parkinson's therapies that may
significantly
and fundamentally improve treatment for people with Parkinson's.
"Improved methods of delivery for apomorphine, which has been shown to
effectively treat 'off-episodes' in motor fluctuation, have been a goal of
pharmaceutical research for at least a decade," says Maurizio Facheris, MD,
MSc,
Associate Director of Research Programs at MJFF. "Preliminary data around
Cynapsus' novel formulation (APL-130277) show promise for a more frequent
and
effective use of this dopaminergic drug. We are hopeful that these
clinical
studies will support this promise, and drive APL-130277 further along the
pipeline of therapeutic development."
"We are grateful to The Michael J. Fox Foundation, as well as their
internal and
external reviewers, for having judged our APL-130277 project to be worthy
of
support," said Mr. Anthony Giovinazzo, President and Chief Executive
Officer of
Cynapsus. "We are optimistic that APL-130277 has the potential to help
many of
the existing Parkinson's patients manage their daily quality of life, the
use of
caregivers and the use of their Levodopa treatments."
Dr. Albert Agro, the Principal Investigator for the study and the Chief
Medical
Officer of Cynapsus added: "The Foundation's support with this
pre-bioequivalence clinical study will be instrumental in helping us
complete the
requirements recommended by the US FDA in our Pre-IND meeting. We have
confidence that our sublingual film strip will succeed in achieving a
pharmacokinetic profile that will satisfy requirements of the US FDA's
505(b)2
approval process and lead to a timely NDA submission sometime in 2014."
About APL-130277 and Apomorphine
Apomorphine is a highly under-utilized medication in Parkinson's disease.
Despite its very strong efficacy and rapid onset of action, patients find
injections painful and delay or resist use of the drug until the very
latest
stages of Parkinson's disease progression. Physicians find the initiation
of
dosing cumbersome because of (a) an in-clinic procedure to determine
tolerability to the drug and (b) training of patients in the use of the
subcutaneous (sc) injection pen device. Eliminating some of these barriers
are
key objectives of Cynapsus' APL-130277.
APL-130277 is an innovative, fast-dissolving, sublingually-administered
thin-film product for use as rescue medication for intermittent OFF
episodes in
Parkinson's disease. The product is easy to self-administer under the
tongue and
dissolves immediately in saliva. The result is a fast and reliable uptake
of the
drug and pharmacokinetics (i.e. the amount of drug in a specified period of
time) that closely mimic the injection, but without the needle or scarring
and
inflammation associated with the injection.
Cynapsus has tested prototype optimizations in-vivo PK models and a lead
candidate was selected. A Pilot PK Study (CTH101) completed in December
2011
measured the pharmacokinetic profile of a single 3mg dose APL-130277 in 15
Healthy Volunteers. APL-130277 showed a rapid onset of absorption and PK
profile similar to the injection form of the drug. Results of a second
Pilot PK
Study (CTH102) are expected to be available by September 2012.
About Parkinson's Disease
Parkinson's disease is a chronic, degenerative neurological disorder that
results from the loss of dopamine-producing nerve cells in the brain.
Current
treatments for Parkinson's disease are able to reduce the symptoms of the
disease but are not able to treat the underlying neurodegenerative
processes
that lead to a decline in physical and cognitive functions that affects
some
patients with Parkinson's disease. It is estimated that over one million
people
in the United States and 5 million people globally are living with
Parkinson's
disease. According to the National Institute of Neurodegenerative Disease
and
Stroke, the average age of onset is 60, though some people are diagnosed at
age
40 or younger.
About The Michael J. Fox Foundation for Parkinson's Research
As the world's largest private funder of Parkinson's research, The Michael
J.
Fox Foundation is dedicated to accelerating a cure for Parkinson's disease
and
improved therapies for those living with the condition today. The
Foundation
pursues its goals through an aggressively funded, highly targeted research
program coupled with active global engagement of scientists, Parkinson's
patients, business leaders, clinical trial participants, donors and
volunteers.
In addition to funding more than $297 million in research to date, the
Foundation has fundamentally altered the trajectory of progress toward a
cure.
Operating at the hub of worldwide Parkinson's research, the Foundation
forges
groundbreaking collaborations with industry leaders, academic scientists
and
government research funders; increases the flow of participants into
Parkinson's
disease clinical trials with its online tool, Fox Trial Finder; promotes
Parkinson's awareness through high-profile advocacy, events and outreach;
and
coordinates the grassroots involvement of thousands of Team Fox members
around
the world. Now through December 31, 2012, all new and increased giving to
The
Michael J. Fox Foundation, as well as gifts from donors who have not given
since
2010 or earlier, will be matched on a dollar-for-dollar basis with the
$50-million Brin Wojcicki Challenge, launched by Sergey Brin and Anne
Wojcicki.
For more information, visit: www.michaeljfox.org;
www.facebook.com/michaeljfoxfoundation.
About Cynapsus Therapeutics
Cynapsus is a specialty pharmaceutical company developing an improved
dosing
formulation of an approved drug used to treat the symptoms of Parkinson's
disease. Over one million people in the United States and an estimated 5
million
people globally suffer from Parkinson's disease. Parkinson's disease is a
chronic and progressive neurodegenerative disease that impacts motor
activity,
and its prevalence is increasing with the aging of the population. Based on
the
IMPACT Registry Study and the results of Cynapsus' Global 500 Neurologists
Survey, is estimated that between 25 percent and 50 percent of patients
experience "OFF episodes" in which they have impaired movement or speaking
capabilities. Current medications only control the disease's symptoms, and
most
drugs become less effective over time as the disease progresses.
Cynapsus' lead drug candidate, APL-130277, is an easy-to-administer,
fast-acting
and oral reformulation of an approved drug, apomorphine, used to rescue
patients
from OFF episodes. Cynapsus is focused on rapidly maximizing the value of
APL-130277 by completing pivotal studies in advance of a New Drug
Application
expected to be submitted in 2014. Cynapsus anticipates out-licensing to an
appropriate pharmaceutical partner before such an application is submitted.
More information about Cynapsus (CTH: TSX-V) is available at
www.cynapsus.ca and
at the System for Electronic Document Analysis and Retrieval (SEDAR) at
www.sedar.com.
Forward Looking Statements
This announcement contains "forward-looking statements" within the meaning
of
applicable Canadian securities legislation. Generally, these
forward-looking
statements can be identified by the use of forward-looking terminology such
as
"plans", "expects" or "does not expect", "is expected", "budget",
"scheduled",
"estimates", "forecasts", "intends", "anticipates" or "does not
anticipate", or
"believes" or variations of such words and phrases or state that certain
actions, events or results "may", "could", "would", "might" or "will be
taken",
"occur" or "be achieved". Forward-looking statements are subject to known
and
unknown risks, uncertainties and other factors that may cause the actual
results, level of activity, performance or achievements of Cynapsus to be
materially different from those expressed or implied by such
forward-looking
statements, including but not limited to those risks and uncertainties
relating
to Cynapsus' business disclosed under the heading "Risk and Uncertainties"
in
"Management's Discussion and Analysis of Operating Results and Financial
Condition" for the year ended December 31, 2011, and its other filings with
the
various Canadian securities regulators which are available online at
www.sedar.com. Although Cynapsus has attempted to identify important
factors
that could cause actual results to differ materially from those contained
in
forward-looking statements, there may be other factors that cause results
not to
be as anticipated, estimated or intended. There can be no assurance that
such
statements will prove to be accurate, as actual results and future events
could
differ materially from those anticipated in such statements. Accordingly,
readers should not place undue reliance on forward-looking statements.
Cynapsus
does not undertake to update any forward-looking statements, except in
accordance with applicable securities laws.
The TSX Venture Exchange Inc. has not reviewed and does not accept
responsibility for the adequacy or accuracy of this press release.
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Source: Cynapsus Therapeutics Inc. via Thomson Reuters ONE
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