Rakovina Therapeutics Presents Preclinical Data Supporting Potential Broad Anticancer Activity of kt-4000 Series at the American Association of Cancer Research (AACR) Annual General Meeting
12 April 2022 - 11:00PM
Rakovina Therapeutics Inc. (TSX-V: RKV) (“the Company”), a
biopharmaceutical company committed to advancing new cancer
therapies based on novel DNA-damage response (DDR) targeting
technologies, is pleased to announce the Company’s poster
presentation at the AACR Annual Meeting.
Rakovina Therapeutics presentation entitled
Evaluation of a Novel Class of Bifunctional DNA Alkylating PARP
Inhibitors was delivered during the Combination Therapeutics
session on April 11, 2022 and highlights pre-clinical research
related to its novel kt-4000 series. The data presented suggested
promising activity for bi-functional kt-4000 series compounds.
Rakovina Therapeutics poster presentation will
be made available on the company’s website following the conclusion
of the AACR Annual Meeting.
Presentation Summary and Overview of
Rakovina Therapeutics kt-4000 series drug candidates.
kt-4000 represents a novel class of small
molecule drug candidates that combine potent inhibition of
polyADP-ribose polymerase (PARP) with DNA alkylating functionality
in a single molecule.
PARP is a key enzyme in the base-excision repair
(BER) pathway, which is an important DNA-damage response mechanism
involved in the repair of DNA single-strand breaks. Cells that are
deficient in other repair mechanisms, such as homologous
recombination (HR) repair, become highly dependent on BER for
survival.
PARP inhibitors are important targeted cancer
therapies that take advantage of HR-deficient cell’s dependence on
BER. FDA-approved PARP inhibitors have become important in the
treatment of HR-deficient tumors such as BRCA-mutant breast and
ovarian cancers. However, PARP inhibitors are less active against
HR-proficient cells that are not dependent on BER for
DNA-repair.
In published laboratory studies, artificially
induced DNA-damage has led to effective killing of HR-proficient
cancer cells by PARP-inhibitors. Cancer chemotherapies known as
alkylating agents induce DNA single-strand breaks, which activate
BER. Published studies demonstrate that when PARP activity is also
inhibited, the cell becomes “stalled” leading to cell death by
apoptosis.
While this has been effective in a laboratory
setting, the combination of the two types of treatment in clinical
practice has been limited by toxicity.
Rakovina Therapeutics’ kt-4000 series aims to
build upon the demonstrated success of the combined mechanism while
reducing the potential for multi-drug toxicity.
The data presented demonstrate that, following
treatment, representative kt-4000 series drug candidates release an
alkylating agent resulting in increased expression of γH2AX, a DNA
damage marker, in cancer cells. kt-4000 drug candidates
simultaneously exhibit potent PARP inhibition at low nanomolar
concentrations. The combined effect leads to G2/M cell cycle arrest
and cell death in HR-proficient cancer cells, normally resistant to
PARP inhibitor treatment.
“The data presented at the AACR meeting
demonstrate that kt-4000 series compounds provide, in a single
molecule, potent DNA-damage, inhibition of repair and cell-cycle
arrest similar to what was observed in prior laboratory studies
employing two separate treatments,” said Dr. Mads Daugaard,
Rakovina Therapeutics president and chief scientific officer.
“Furthermore, the anti-cancer mechanism observed appears to be
distinct from FDA-approved PARP-inhibitors suggesting the potential
for broad utility of drug candidates derived from this class.”
Select kt-4000 lead candidates are being
advanced to evaluate pharmacokinetics, preliminary safety profile
and anti-tumor activity in vivo.
About Rakovina Therapeutics
Inc.
Rakovina Therapeutics Inc. is focused on the
development of new cancer treatments based on novel DNA-damage
response (DDR) technologies. The Company has established a pipeline
of novel DNA-damage response inhibitors with the goal of advancing
one or more drug candidates into human clinical trials and
obtaining marketing approval for new cancer therapeutics from
Health Canada, the United States Food and Drug Administration and
similar international regulatory agencies. Further information may
be found at www.rakovinatherapeutics.com.
Additional Information
The TSXV has neither approved nor disapproved
the content of this press release. Neither the TSXV nor its
Regulation Services Provider (as that term is defined in policies
of the TSXV) accepts responsibility for the adequacy or accuracy of
this release.
Notice regarding forward-looking
statements:
This release includes forward-looking statements
regarding the Company and its respective business, which may
include, but is not limited to, statements with respect to the
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result of known and unknown risk factors and uncertainties
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industry, economic factors, regulatory factors, the equity markets
generally and risks associated with growth and competition.
Although the Company has attempted to identify important factors
that could cause actual actions, events, or results to differ
materially from those described in forward-looking statements,
there may be other factors that cause actions, events, or results
to differ from those anticipated, estimated or intended. No
forward-looking statement can be guaranteed. Except as required by
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risk factors and their potential effects, copies of which may be
accessed through the Company’s profile page at www.sedar.com.
Contact:
Rakovina Therapeutics
Inc.David HymanChief Financial OfficerEmail:
info@rakovinatherapeutics.com |
Investor Relations
ContactIR@rakovinatherapeutics.com Media
ContactMEDIA@rakovinatherapeutics.com |
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