WPD Pharmaceuticals Enters into Collaborative Agreement for WP1122, Receives Supply and Appoints New CFO
17 August 2020 - 11:52PM
WPD Pharmaceuticals Inc. (“WPD” or the “Company”) (CSE:
WBIO) (FSE: 8SV1), a clinical stage pharmaceutical
company
, announces that it has entered into a
collaborative agreement with Dermin Sp. z o.o., a Polish biotech
research company.
WPD previously held the rights to the compound
WP1122 under sublicense in 29 countries mostly in Europe and Asia,
and under the collaborative agreement has now added Poland, except
for the WP1122 rights to treat gliomas in Poland. Under the
collaborative agreement, WPD is not required to pay Dermin or grant
a royalty for the rights transferred, but is required to provide
Dermin with all its research data, if any, which Dermin may use for
the further development of WP1122 as an anti-glioma drug.
Two rounds of independent studies have confirmed
the antiviral activity of WP1122 against Covid-19 (see 2 separate
WPD news releases dated April 9, 2020 and a WPD news release dated
July 22, 2020). In addition, Dermin is also transferring to WPD its
current research supply of the compound WP1122, which WPD considers
may be sufficient for 3 to 6 months’ worth of non-GMP testing once
testing begins, expected in Q4 2020.
WPD has not conducted its own independent
confirmation testing of WP1122 and is relying solely on the
information of other parties in providing information on WP1122 to
WPD’s shareholders. WPD is not making any express or implied claims
that WP1122 has the ability to eliminate, cure or contain the
Covid-19 (or SARS-2 Coronavirus) at this time. WPD does not have a
bio-safety level 3 (SBL-3) laboratory, needed to conduct research
on viruses. It outsources its research and development to contract
research organizations (“CRO”) which have the required level of
safety protocols and equipment.
The Company is not making any express or implied claims that its
product has the ability to eliminate, cure or contain the Covid-19
(or SARS-2 Coronavirus) at this time.
Michael Malana appointed as
CFO
The Company is pleased to announce the
appointment of Michael Malana of Richmond, B.C. as its CFO. Michael
has considerable and continuous experience over the past 15 years
acting as CFO, Corporate Controller and/or Corporate Secretary for
a range of Canadian public companies listed on the TSX, TSXV and
CSE. The Company is looking to Mr. Malana for his regulatory and
stock exchange knowledge and for added value as a detailed and
meticulous accountant.
The Company has accepted the resignation of
Chris Cherry as CFO, who graciously agreed to be acting CFO
starting in December 2019. The Company thanks Mr. Cherry for his
service and wishes him well in future endeavours.
About WPD Pharmaceuticals
WPD is a biotechnology research and development
company with a focus on oncology and virology, namely research and
development of medicinal products involving biological compounds
and small molecules. WPD has licensed in certain countries 10
novel drug candidates with 4 that are in clinical development
stage. These drug candidates were researched at medical
institutions, and WPD currently has ongoing collaborations with
Wake Forest University and leading hospitals and academic centers
in Poland.
WPD has entered into license agreements with
Wake Forest University Health Sciences and sublicense agreements
with Moleculin Biotech, Inc. and CNS Pharmaceuticals, Inc.,
respectively, each of which grant WPD an exclusive, royalty-bearing
sublicense to certain technologies of the licensor. Such agreements
provide WPD with certain research, development, manufacturing and
sales rights, among other things. The sublicense territory
from CNS Pharmaceuticals and Moleculin Biotech includes for most
compounds 30 countries in Europe and Asia, including Russia.
On Behalf of the Board
‘Mariusz Olejniczak’ Mariusz Olejniczak CEO, WPD
Pharmaceuticals
Contact
Investor Relations Email: investors@wpdpharmaceuticals.comTel:
604-428-7050 Web: www.wpdpharmaceuticals.com Neither the
Canadian Securities Exchange nor the Investment Industry Regulatory
Organization of Canada accepts responsibility for the adequacy or
accuracy of this release.
This press release contains forward-looking
statements. Forward-looking statements are statements that
contemplate activities, events or developments that the Company can
develop effective drugs against cancer and possibly viruses; and
that research of WP1122 will commence during 2020; and that its
supply of WP1122 is sufficient for 3 to 6 months of testing.
Factors which may prevent the forward looking statement from being
realized include that our supply of compounds for testing may not
be sufficient for our needs; lack or funds, permits, subcontractors
or other factors may delay our plans; competitors or others may
successfully challenge a granted patent and the patent could be
rendered void; we may be unable to raise sufficient funding for our
research; we may be unable to expend sufficient funds on research
to keep our sublicense rights; our grant applications may not be
successful or if successful, we may not meet the requirements to
receive the grants awarded; that our drugs don’t provide positive
treatment, or if they do, the side effects are damaging; and
competitors may develop better or cheaper drugs; our plans may be
delayed; we may not be able to get commercial quantities of our
drugs made; and we may be unable to obtain regulatory approval for
any drugs we develop. Readers should refer to the risk disclosure
included from time-to-time in the documents the Company files on
SEDAR, available at www.sedar.com. Although the Company
believes that the assumptions inherent in these forward-looking
statements are reasonable, they are not guarantees of future
performance and, accordingly, they should not be relied upon and
there can be no assurance that any of them will prove to be
accurate. Finally, these forward-looking statements are made
as of the date of this press release and the Company assumes no
obligation to update them except as required by applicable law.
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