Pascal Biosciences Provides Year-End Investor Update and Reviews Upcoming Milestones
20 Dezember 2018 - 2:00PM
- 2018 pipeline
expansion includes lead cannabinoid-based cancer
therapeutic- Clinical trial in glioblastoma to
begin in 2019
Pascal Biosciences Inc. (TSX.V:PAS) (“Pascal” or the “Company”), a
drug discovery and development company, today announced a year-end
review of accomplishments during 2018 and insight into plans for
2019.
“Pascal today is a much different company from
that of just a year ago. We have two promising cannabinoid
therapeutic programs close to clinical evaluation, secured a
Schedule I research license for cannabinoid research and have
strengthened our leadership team to support our development
efforts,” said Dr. Patrick Gray, CEO of Pascal. “We look forward to
beginning clinical evaluation of our product ST-403 in glioblastoma
and further advancing our promising cannabinoid research efforts in
the coming year.”
2018 Highlights
Research:
- Announced discovery that cannabis contains compounds capable of
stimulating the immune system to destroy tumor cells. While
cannabinoids have long been known to be helpful in treating cancer
symptoms like nausea and pain, Pascal was the first to identify a
mechanism in which cannabinoids may provide a direct benefit in
immunotherapy. We believe certain cannabinoids may activate the
immune system to destroy cancer cells and hopefully improve the
efficacy of checkpoint inhibitors, the most exciting class of new
therapeutics. Pascal is planning to test select compounds in
volunteers and patients.
- Received a US Drug Enforcement Administration (DEA) Schedule I
Research license to enable cannabinoid research work. Very few
research organizations obtain a Schedule I license and most are
universities. Obtaining the license is a very rigorous process and
enables Pascal to conduct research on cannabinoids, to develop a
cannabinoid product, and to conduct clinical trials on cancer
patients.
- In October Pascal licensed a cannabinoid-based product for the
treatment of glioblastoma and brain metastases. Glioblastoma is a
devastating disease that strikes 15,000 patients each year in North
America, and the median survival rate is only 12 to 17 months. Our
compound is very effective in a mouse model of glioblastoma, and
Pascal plans to begin human clinical studies in 2019. This
program is the culmination of 20 years of effort by renowned
cannabis researcher Dr. Nephi Stella, founder and co-director of
the University of Washington Center for Cannabis Research. Dr.
Stella is now a consultant for Pascal, and he has been very helpful
with both of Pascal’s cannabinoid programs.
Additions to Board and Management Team:
- Julie Eastland was appointed to the Pascal Board of Directors
this summer. Julie is an accomplished financial executive, with
more than 25 years of experience in public and private
biotechnology companies. Most recently she was Chief Business
Officer and Chief Financial Officer of Cascadian Therapeutics,
where she negotiated and managed their acquisition by Seattle
Genetics, in a deal valued at $810M. Julie has the financial and
corporate development experience that Pascal needs going forward.
- Pascal strengthened its leadership team with the appointments
of accomplished executives in therapeutic and business development.
This includes Kevin Egan, Vice President of Business Development.
He has been in biotech for over 30 years and has a proven track
record of negotiating partnering, licensing, and outsourcing
deals. Dr. Tom Deckwerth, Vice President of Therapeutic
Development, has 20 years of industrial experience in therapeutic
development. And Dr. Larry Tjoelker, Vice President of
Research, has over 25 years of research experience in the
biotechnology industry.
“The extensive experience of Julie, Kevin, Tom,
and Larry will be invaluable as we advance our leading
cannabinoid-based programs and explore strategic opportunities,”
said Gray.
Looking ahead to 2019
Pascal is targeting to initiate clinical trials
of ST-403 in glioblastoma next year. Manufacturing efforts have
already begun, and formulation, safety studies, and clinical
studies are all being planned with a strict timeline.
Second, Pascal has put much effort into its
immune-stimulatory cannabinoid program in collaboration with our
founder Dr. Wilf Jefferies at the University of British Columbia.
This work will be published in peer-reviewed scientific articles,
and you will hear a lot more about this program going forward,
including plans for studies in human volunteers and patients.
“The world of drug development is exciting and
promising, but it is also costly and time consuming. Along with the
risk, there is great value in a successful product that provides
benefit to patients,” said Gray. “While we are at an early stage in
this process, we have the faith and enthusiasm that we will be
successful. And we are driven by the knowledge that patients need a
cure. Patients and their families contact us to ask when they
can be tested—this is the reason we come to work each day, and this
is the reason we are driven to make our products available as
quickly as possible.”
About Pascal Biosciences Inc.
Pascal Biosciences is a biotechnology company
focused on advancing innovative approaches for the treatment of
cancer including cannabinoid-based therapeutics and targeted
therapies. The company’s leading cannabinoid portfolio comprises a
small molecule therapeutic, ST-403, that is advancing into clinical
trials for the treatment of glioblastoma, and an immuno-stimulatory
molecule. In addition, Pascal Biosciences is developing a B-cell
targeted antibody for acute lymphoblastic leukemia and an antibody
for calcium channels expressed by the immune system. For more
information, visit www.pascalbiosciences.com.
Investors: invest@pascalbiosciences.com Tel:
206-221-3443
Media Contact: Julie Rathbun Tel:
206-769-9219
DISCLAIMER Certain statements in this press
release contain forward-looking statements within the meaning of
the Private Securities Litigation Reform Act of 1995 or
forward-looking information under applicable Canadian securities
legislation that may not be based on historical fact, including
without limitation statements containing the words “believe”,
“may”, “plan”, “will”, “estimate”, “continue”, “anticipate”,
“intend”, “expect” and similar expressions. Such forward-looking
statements or information involve known and unknown risks,
uncertainties and other factors that may cause our actual results,
events or developments, or industry results, to be materially
different from any future results, events or developments express
or implied by such forward-looking statements or information. Such
factors include, among others, our stage of development, lack of
any product revenues, additional capital requirements, risk
associated with the completion of clinical trials and obtaining
regulatory approval to market our products, the ability to protect
our intellectual property, dependence on collaborative partners and
the prospects for negotiating additional corporate collaborations
or licensing arrangements and their timing. Specifically, certain
risks and uncertainties that could cause such actual events or
results expressed or implied by such forward-looking statements and
information to differ materially from any future events or results
expressed or implied by such statements and information include,
but are not limited to, the risks and uncertainties that: products
that we develop may not succeed in preclinical or clinical trials,
or future products in our targeted corporate objectives; our future
operating results are uncertain and likely to fluctuate; we may not
be able to raise additional capital; we may not be successful in
establishing additional corporate collaborations or licensing
arrangements; we may not be able to establish marketing and the
costs of launching our products may be greater than anticipated; we
have no experience in commercial manufacturing; we may face unknown
risks related to intellectual property matters; we face increased
competition from pharmaceutical and biotechnology companies; and
other factors as described in detail in our filings with the
Canadian securities regulatory authorities at www.sedar.com.
Given these risks and uncertainties, you are cautioned not to place
undue reliance on such forward-looking statements and information,
which are qualified in their entirety by this cautionary statement.
All forward-looking statements and information made herein are
based on our current expectations and we undertake no obligation to
revise or update such forward- looking statements and information
to reflect subsequent events or circumstances, except as required
by law.“Neither the TSX Venture Exchange nor its Regulation
Services Provider (as that term is defined in the policies of the
TSX Venture Exchange) accepts responsibility for the adequacy or
accuracy of this release”
Pascal Biosciences (TSXV:PAS)
Historical Stock Chart
Von Dez 2024 bis Jan 2025
Pascal Biosciences (TSXV:PAS)
Historical Stock Chart
Von Jan 2024 bis Jan 2025