WPD Pharmaceuticals' STAT3 Inhibitor Received FDA Approval of IND Status in Pediatric Brain Cancer Trial
20 Février 2020 - 9:05AM
WPD Pharmaceuticals Inc. (CSE: WBIO)(FSE: 8SV1) (the
“
Company” or “
WPD”), a clinical
stage pharmaceutical company is pleased to provide an update on its
WP1066 drug in the treatment of pediatric brain cancer. Through
Moleculin Biotech, Inc.
(“
Moleculin”)(Nasdaq:MBRX), WPD’s license partner,
the WP1066 drug candidate received FDA approval for Investigational
New Drug ("
IND") status to be used in a Phase 1
clinical trial for the treatment of children with recurrent or
refractory malignant brain tumors.
The request was made by physician researchers at
Emory University, including Dr. Tobey MacDonald, Professor of the
Department of Pediatrics at Emory University School of Medicine,
Director of Pediatric Neuro-Oncology at Aflac Cancer and Blood
Disorders Center and Principle Investigator for this clinical
trial. The trial will be conducted at the Aflac Cancer and
Blood Disorders Center at Children's Healthcare of Atlanta.
Mariusz Olejniczak, CEO of WPD
commented "Receiving FDA approval at any stage of research and
development is important and validates the work on WP1066. WP1066
is currently in a clinical trial for adult patients with
glioblastoma and melanoma metastases to the brain at MD Anderson
Cancer Center, and this is a logical extension of that
research. Preclinical research at Emory University indicated
that WP1066 had a significant anti-tumor effect on medulloblastoma
cell lines, and we feel encouraged by the potentially new
opportunity for treatment of this rare condition."
About Moleculin Biotech, Inc.
Moleculin Biotech, Inc. is a clinical stage
pharmaceutical company focused on the development of a broad
portfolio of oncology drug candidates for the treatment of highly
resistant tumors. The Company's clinical stage drugs are:
Annamycin, a Next Generation Anthracycline, designed to avoid
multidrug resistance mechanisms with little to no cardiotoxicity
being studied for the treatment of relapsed or refractory acute
myeloid leukemia, more commonly referred to as AML, WP1066, an
Immune/Transcription Modulator capable of inhibiting p-STAT3 and
other oncogenic transcription factors while also stimulating a
natural immune response, targeting brain tumors, pancreatic cancer
and hematologic malignancies, and WP1220, an analog to WP1066, for
the topical treatment of cutaneous T-cell lymphoma. Moleculin is
also engaged in preclinical development of additional drug
candidates, including other Immune/Transcription Modulators, as
well as compounds capable of Metabolism/Glycosylation
Inhibition.
For more information about the Company, please
visit http://www.moleculin.com.
About WPD Pharmaceuticals
WPD is a biotechnology research and development
company with a focus on oncology, namely research and development
of medicinal products involving biological compounds and small
molecules. WPD has 10 novel drug candidates with 4 that are
in clinical development stage. These drug candidates were
researched at institutions including MD Anderson Cancer Center,
Mayo Clinic and Emory University, 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.
On Behalf of the Board
‘Mariusz Olejniczak’
Mariusz OlejniczakCEO, WDP Pharmaceuticals
Contact:
Investor RelationsEmail: investors@wpdpharmaceuticals.comTel:
604-428-7050Web: www.wpdpharmaceuticals.com
Cautionary Statements:
Investors are cautioned that, except as disclosed in the
Company’s CSE listing statement, prepared in accordance with the
policies of the CSE, any information released or received with
respect to the transaction may not be accurate or complete and
should not be relied upon. Trading in the securities of the Company
should be considered highly speculative.
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
anticipates will or may occur in the future. Forward-looking
statements in this press release include that our findings could
have a significant impact on understanding the role of STAT3
inhibition and that WPD’s drugs could be developed into novel
treatments for cancer. These forward-looking statements
reflect the Company’s current expectations based on information
currently available to management and are subject to a number of
risks and uncertainties that may cause outcomes to differ
materially from those projected. Factors which may prevent
the forward looking statement from being realized is that
competitors or others may successfully challenge a granted patent
and the patent could be rendered void; that we are unable to raise
sufficient funding for our research; that our drugs don’t provide
positive treatment, or if they do, the side effects are damaging;
competitors may develop better or cheaper drugs; 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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