Rakovina Therapeutics to Present Research Highlighting Small-Molecule Bifunctional Inhibitors of PARP1/2 and HDAC Enzymes at the 36th EORTC-NCI-AACR Symposium in Barcelona Spain
25 October 2024 - 10:30PM
Rakovina Therapeutics Inc. (TSX-V: RKV)
(“Rakovina” or the “Company”), a biopharmaceutical company
committed to advancing new cancer therapies based on novel
DNA-damage response targeting technologies, is pleased to announce
the presentation of its research on novel small-molecule
bifunctional inhibitors of PARP1/2 and HDAC enzymes at the 36th
EORTC-NCI-AARC Symposium in Barcelona, Spain, on October 25, 2024.
Rakovina’s novel class of bifunctional small molecule compounds,
known as kt-3000 series, has demonstrated potent dual inhibition of
PARP1/2 and HDAC enzymes in preclinical studies. Compared to
single-function inhibitors such as olaparib (PARP) and vorinostat
(HDAC), dual-function kt-3000 compounds demonstrate greater potency
against both HR-deficient and proficient cancer cells.
Based on these results, the Company intends to explore
formulations of the lead compound, kt-3283, to support potential
advancement to human clinical trials, while continuing to further
medicinal chemistry efforts that refine properties of the
class.
“The kt-3000 series represents a significant advancement toward
overcoming treatment resistance to first-generation
PARP-inhibitors. These bifunctional PARP+HDAC inhibitors could
enable us to effectively address resistance in various cancers
while minimizing toxicity associated with traditional combination
therapies,” said Rakovina Therapeutics Executive Chairman Jeffrey
Bacha.
“We are excited to present our findings at the symposium and to
continue advancing these promising compounds toward clinical
development,” he added.
Presentation Details:
Title:
Small-molecule bifunctional inhibitors of PARP1/2 and HDAC
enzymesPresentation Date: October 25,
2024Abstract Number: 338
About Rakovina Therapeutics Inc.Rakovina
Therapeutics Inc. is focused on the development of new cancer
treatments based on novel DNA-damage response 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
The TSXV has neither approved nor disapproved the content of
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responsibility for the adequacy or accuracy of this release.
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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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certain specified dates or at all and could differ materially as a
result of known and unknown risk factors and uncertainties
affecting the Company, including risks regarding the medical device
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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accessed through the Company’s profile page at www.sedar.com.
For Further Information, Contact:Jeffrey Bacha,
BSC, MBAExecutive Chairman and
Directorinfo@rakovinatherapeutics.comInvestor Relations and
Media:Ira M. GostinInvestor RelationsIR@rakovinatherapeutics.com
775-391-0213
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