Cynapsus Therapeutics Reports First Quarter 2014 Financial Results and Recent Developments
07 Mai 2014 - 11:30PM
Marketwired
Cynapsus Therapeutics Reports First Quarter 2014 Financial Results
and Recent Developments
TORONTO, ONTARIO--(Marketwired - May 7, 2014) - Cynapsus
Therapeutics Inc. (TSX-VENTURE:CTH)(OTCQX:CYNAF), a specialty
pharmaceutical company developing a convenient and easy to use
sublingual (oral) thin film strip for the acute rescue of "off"
motor symptoms of Parkinson's disease, today announced its results
for the three months ended March 31, 2014. Unless specified
otherwise, all amounts are in Canadian dollars.
Anthony Giovinazzo, President and Chief Executive Officer of
Cynapsus, stated: "The first quarter of 2014 has been pivotal in
establishing the foundation for Cynapsus to complete the next
de-risking steps for the remainder of the year. The completion of
the CTH-103 and CTH-104 clinical studies in the quarter, as well as
the closing of a $25,000,000 financing in April, were significant
accomplishments. Management is now primarily focused on the
execution of the following three clinical studies: (1) the CTH-105
pilot study in patients with Parkinson's disease in Q3 2014; (2)
the CTH-200 bioavailability study in Q3-Q4 2014; and (3) the
CTH-300a efficacy study in apomorphine naïve patients by the end of
Q4 2014. We look forward to reporting our progress."
Financial Highlights
- Cash and cash equivalents on hand at March 31, 2014 of
$1,259,058 (December 31, 2013: $2,289,046).
- Subsequent to the end of the quarter, on April 15, 2014, the
Company announced the closing of a short form prospectus offering
for aggregate gross proceeds of $25,000,000.
- Net loss of $1,210,272 for the three months ended March 31,
2014 (March 31, 2013: Net loss of $351,593).
- Report 78,618,149 common shares outstanding at March 31, 2014
(December 31, 2013: 38,884,009 common shares).
Operational Highlights
The following achievements were made during the first three
months of 2014:
- Cynapsus announced results for the CTH-103 clinical trial. On
January 13, 2014, Cynapsus announced positive top line data of the
Comparative Biostudy (CTH-103) of APL-130277. The CTH-103 study was
designed as a three-dose (10mg, 15mg and 25mg) active comparator,
placebo-controlled, randomized cross-over trial to examine the
pharmacokinetic profile of sublingual administered APL-130277
compared to (2mg, 3mg and 4mg) subcutaneous injections of
apomorphine in healthy volunteers. The 10mg and 15mg APL-130277
sublingual thin film strips were crossed over to 2mg and 3mg
subcutaneous injections, with N=15 and N=14 for the two cohorts,
respectively. The intent in the CTH-103 study for the third cohort
was to compare the 25mg sublingual thin film strip (APL-130277) to
the 4mg subcutaneous injection, but this third cohort could not be
dosed due to the dose-limiting adverse events experienced with the
3mg subcutaneous injection. The 15mg APL-130277 side effects were
mild-to-moderate and not dose limiting. As a result, the Company
completed the CTH-104 study, a single arm, healthy volunteer
pharmacokinetic study to look at the 25mg APL-130277 sublingual
strip (without a crossover to the injection).
- Cynapsus announced the appointment of Nan Hutchinson to the
Board of Directors. On February 13, 2014, Cynapsus announced the
appointment of a new director, Nan Hutchinson, who has more than
twenty-five years of pharmaceutical experience spanning all aspects
of commercialization, including strategic planning, marketing,
business development, sales leadership, talent identification and
development.
- Cynapsus announced results for the CTH-104 clinical trial. On
March 28, 2014, Cynapsus announced interim summary results of the
CTH-104 study of APL-130277. Final study results were announced on
April 24, 2014. CTH-104 study was a single dose, single arm,
placebo-controlled, healthy volunteer pharmacokinetic study, which
was designed to examine the pharmacokinetic profile of the 25mg
dose of APL-130277. In total, 13 subjects completed the study (11
active and 2 placebo). The results from the CTH-104 study in human
healthy volunteers demonstrated dose proportionality of the doses
tested in CTH-103 (10mg and 15mg) and CTH-104 (25mg). In addition,
the results of CTH-104 showed that the 25mg dose was sustained over
an extended period of time (162 minutes) above the minimal
efficacious plasma concentration of apomorphine (approximately
3ng/ml), which is believed to be a level demonstrating symptomatic
relief of "off" symptoms.
- Cynapsus announced the completion of a $25 million short form
prospectus financing. Subsequent to the end of the first quarter,
on April 15, 2014, the Corporation announced that it completed a
short form prospectus offering of units for maximum aggregate gross
proceeds of $25 million. Cynapsus intends to use the net proceeds
from the offering to complete the U.S. clinical development of its
Parkinson's drug candidate, APL-130277.
Annual and Special Meeting of Shareholders
Earlier in the day, on May 7, 2014, the Company held its Annual
and Special Meeting of Shareholders. The following eight (8)
individuals were re-elected as Directors of the Company for the
ensuing year: Mr. Anthony Giovinazzo, Mr. Ronald Hosking, Mr. Tomer
Gold, Ms. Nan Hutchinson, Dr. Perry Molinoff, Mr. Ilan Oren, Dr.
Alan Ryley and Ms. Rochelle Stenzler. McGovern, Hurley, Cunningham,
LLP was also re-appointed as the auditors of the Company for the
ensuing year to serve at such remuneration as may be fixed by the
Board of Directors. In addition, the stock option plan of the
Company was approved, including the reservation for issuance of a
"rolling" maximum number of 10% of the shares issuable under the
stock option plan. The shareholders of the Company also voted in
favour of amending the Company's stock option plan to allow for
automatic extensions of the expiry date of stock options if the
expiry date occurs during a blackout period, which amendment
remains subject to the approval of the TSX Venture Exchange.
About Cynapsus Therapeutics
Cynapsus is a specialty pharmaceutical company developing a
convenient and easy to use sublingual (oral) thin film strip for
the acute rescue of "off" motor symptoms of Parkinson's disease.
Cynapsus' drug candidate, APL-130277, is an easy-to-administer,
fast-acting reformulation of apomorphine, which is the only
approved drug (in the United States, Europe, Japan and other
countries) to rescue patients from "off" episodes. Cynapsus is
focused on maximizing the value of APL-130277 by completing pivotal
studies in advance of a New Drug Application ("NDA") expected to be
submitted in 2016.
Over one million people in the U.S. and an estimated 4 to 6
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 a recent
study and the results of the Corporation's Global 500 Neurologists
Survey, it 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.
More information about Cynapsus (TSX-VENTURE:CTH)(OTCQX:CYNAF)
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 securities laws. 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 Factors" in its March 26, 2014, Annual Information
Form 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.
Neither the TSX Venture Exchange nor the OTCQX International has
approved or disapproved of the contents of this press release.
Cynapsus TherapeuticsAnthony GiovinazzoPresident and CEO(416)
703-2449 x225ajg@cynapsus.caCynapsus TherapeuticsAndrew WilliamsCOO
& CFO(416) 703-2449 x253awilliams@cynapsus.ca
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