Helix BioPharma Corp. collaborator ProMab Biotechnologies to present at the CAR-TCR Summit 2018 in Boston
September 04 2018 - 5:05PM
Helix BioPharma Corp. (TSX: HBP), (FSE: HBP) (“Helix” or the
“Company”), an immuno-oncology company developing innovative drug
candidates for the prevention and treatment of cancer, today
announced that its collaborator ProMab Biotechnologies, Inc.
(“ProMab”) will present at the CAR-TCR Summit 2018 being held from
September 4th - 7th, 2018 in Boston, Massachusetts.
Dr. Vita Golubovskaya, Director, R&D, BD of
Promab Biotechnologies will present on September 5th at
12:25pm. The title of the presentation is “Novel CAR-T Cells
Against Solid and Hematological Cancers”. Dr. Golubovskaya’s
presentation will include certain preclinical data from the
multiple myeloma project currently in collaboration with Helix.
Helix continues to aim for a possible
first-in-human CAR-T study in 2019. To achieve this goal, Helix’s
wholly-owned Polish subsidiary Helix Immuno-Oncology (“HIO”) will
be leading the preclinical and clinical development program in
Poland prioritizing a possible European clinical submission. Helix
and HIO are engaging experts to advise on the program and are
currently securing the necessary financial resources to meet the
project timelines.
About Helix BioPharma Corp.
Helix BioPharma Corp. is an immuno-oncology
company specializing in the field of cancer therapy. The company is
actively developing innovative products for the prevention and
treatment of cancer based on its proprietary technologies. Helix’s
product development initiatives include its novel L-DOS47 new drug
candidate and Chimeric Antigen Receptor (“CAR”) based cell
therapies. Helix is currently listed on the TSX and FSE under the
symbol “HBP”.
About Helix Immuno-Oncology
S.A.
Helix Immuno-Oncology S.A. is a wholly-owned
subsidiary of Helix BioPharma Corp., a research company
specializing in the development of novel anti-tumour therapies in
the field of immune-oncology. The company’s development initiatives
include V-DOS47 drug candidate for Triple Negative Breast Cancer
treatment, cellular therapies as well as combination of
thereof.
About ProMab
Biotechnologies
ProMab Biotechnologies is a US biotechnology
company that develops and commercializes recombinant proteins,
custom monoclonal antibodies, CAR-T products through the
integration of bioinformatics, gene cloning, protein expression and
purification, and immunology, using novel high-throughput
technologies.
Investor Relations
Helix BioPharma Corp.9120 Leslie Street, Suite
205Richmond Hill, Ontario, L4B 3J9Tel: 905-841-2300Email:
ir@helixbiopharma.com
Cautionary Statements
This news release may contain forward-looking
statements and information (collectively, "forward-looking
statements") within the meaning of applicable Canadian securities
laws. Forward-looking statements are statements and
information that are not historical facts but instead include
financial projections and estimates; statements regarding plans,
goals, objectives, intentions and expectations with respect to
Helix’s future business, operations, research and development,
including Helix’s activities relating to its drug development
program, the anticipated timelines for the commencement or
completion of certain activities, including enrolment of patients,
the expansion of the DOS47 platform into other compounds and
indications and other information in future periods.
Forward-looking statements, which may be identified by words
including, without limitation, “may”, “improve”, “planned”,
“possible”, “postulated”, “enhances”, “potential”, “development”,
“unique”, “expects”, “plans”, “will”, “intends”, “pending”,
“objective”, “exploring”, “projected”, and other similar
expressions, are intended to provide information about management’s
current plans and expectations regarding future operations.
Although Helix believes that the expectations
reflected in such forward-looking statements are reasonable, such
statements involve risks and uncertainties that may cause actual
results or events to differ materially from those anticipated and
no assurance can be given that these expectations will be realized,
and undue reliance should not be placed on such statements. Risk
factors that could cause actual results or events to differ
materially from the forward-looking statements include, without
limitation: (i) Helix’s ability to operate as a going concern being
dependent mainly on securing sufficient additional financing in
order to fund its ongoing research and development and other
operating activities; (ii) the generally inherent uncertainty
involved in scientific research and drug development and those
specific to Helix’s pre-clinical and clinical development programs
(DOS47, L-DOS47, V-DOS47 and CAR-T); (iii) difficulties in
predicting accurate timelines for the commencement or completion of
certain activities including those in support of ongoing clinical
trials; (iv) positive preliminary results from early-stage clinical
trials may not be indicative of the final results from the trial or
be indicative of favorable outcomes in later-stage clinical trials;
(v) delays or inability to complete clinical trials successfully
and the long lead-times and high costs associated with obtaining
regulatory approval to market any product which may result from
successful completion of such trials; (vi) clinical data may not
demonstrate adequate efficacy and safety to result in regulatory
approval to market any of Helix’s product candidates in any
jurisdiction; (vii) economic and market conditions may become worse
and market shifts may require a change in strategic focus; and
(viii) those risks and uncertainties affecting Helix as more fully
described in Helix’s most recent Annual Information Form, including
under the headings “Forward-Looking Statements” and “Risk Factors”,
filed under Helix’s profile on SEDAR at www.sedar.com (together,
the “Helix Risk Factors”). Certain material factors and assumptions
are applied in making the forward-looking statements, including,
without limitation, that sufficient financing will be obtained in a
timely manner to allow Helix to continue operations and implement
its clinical trials in the manner and on the timelines anticipated
and that the Helix Risk Factors will not cause Helix’s actual
results or events to differ materially from the forward-looking
statements. These cautionary statements qualify all such
forward-looking statements.
Forward-looking statements and information are
based on the beliefs, assumptions, opinions, plans and expectations
of Helix’s management on the date of this news release, and the
Company does not assume any obligation to update any
forward-looking statement or information should those beliefs,
assumptions, opinions, plans or expectations, or other
circumstances change, except as required by law.
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