Rakovina Therapeutics Presents Preclinical Data on its Novel kt-3000 Series at the 2022 AACR Special Conference on Sarcomas
May 11 2022 - 8:00AM
Rakovina Therapeutics Inc. (TSX-V: RKV) (“the Company”), a
biopharmaceutical company committed to advancing new cancer
therapies based on novel DNA-damage response (DDR) technologies, is
pleased to announce the presentation of new data during the 2022
AACR Special Conference on Sarcomas in Montreal, Canada.
Rakovina Therapeutics’ presentation entitled In
vitro efficacy of a novel dual PARP-HDAC Inhibitor in Ewing sarcoma
highlighted the Company’s development of its novel kt-3000 series
drug candidates as a potential treatment of Ewing sarcoma and other
soft tissue tumors.
“These newly presented in vitro data suggest
promising activity for our novel kt-3000 series drug candidates as
a potential treatment for Ewing sarcoma and other
treatment-resistant cancers,” said Professor Mads Daugaard, PhD,
president & chief scientific officer of Rakovina Therapeutics
Inc. “Based on these outcomes, select kt-3000 candidates have now
been advanced to evaluation of pharmacokinetics, safety and
anti-tumour activity in vivo.”
Ewing sarcoma is a cancer that occurs primarily
in the bone or soft tissues and is the second most common type of
bone cancer affecting children and young adults. Approximately
thirty percent of patients will experience recurrence within five
years following treatment. The prognosis for patients with
recurrent or progressive Ewing sarcoma is poor with average
survival from the time of relapse of only 14 months.
Current treatments for Ewing sarcoma include
chemotherapy, surgery and radiotherapy. Long-term side effects of
these treatments can include heart and lung problems, emotional and
learning difficulties, growth issues and secondary cancers
associated with chemotherapy or radiation. The development of new
and improved treatments for Ewing sarcoma represents a significant
unmet medical need.
FDA-approved poly(ADP)-ribose polymerase (PARP)
inhibitors have previously been studied in clinical trials as a
potential treatment for Ewing sarcoma but showed only limited
clinical benefit. Pre-clinical studies have revealed the potential
for synergy in the treatment of Ewing sarcoma by combining a PARP
inhibitor with inhibition of histone deacetylase (HDAC) enzymes. In
clinical practice, however, the benefits of combination treatments
are often limited due to differing pharmacokinetics and overlapping
toxicities requiring sequential administration.
Rakovina Therapeutics’ kt-3000 series represents
a novel class of bi-functional small-molecule drug candidates that
has been designed to combine inhibition of both PARP and HDAC in a
single molecule as a potentially more viable approach to providing
meaningful clinical benefit to patients.
New kt-3000 data presented by Rakovina
Therapeutics’ researchers at the AACR Special Conference on
Sarcomas demonstrate that:
- Rakovina
Therapeutics’ kt-3283 prototype lead drug candidate exhibits potent
bi-functional activity as evidenced by inhibition of PARP and
PARylation at a low nanomolar potency plus potent inhibition of
HDAC enzyme activity;
- kt-3283
treatment reduced viability of Ewing sarcoma cells >25 fold more
potently than an FDA-approved PARP inhibitor or FDA-approved HDAC
inhibitor;
- Treatment of
Ewing sarcoma cancer cells with kt-3283 resulted in increased
S-phase and G2/M cell cycle arrest compared to single-agent
treatment with an FDA-approved PARP inhibitor or HDAC inhibitor, or
the combination of the two PARP and HDAC inhibitors; and
- The kt-3000
bi-functional anti-cancer mechanism results in significantly higher
DNA damage to Ewing sarcoma cancer cells compared to single-agent
treatment with a PARP inhibitor or an HDAC inhibitor, both of which
caused little or no DNA-damage to Ewing sarcoma cancer cells
following equimolar treatment in the same assay.
Rakovina Therapeutics has previously presented
preclinical data at peer reviewed scientific meetings demonstrating
the potential of kt-3000 series drug candidates against
treatment-resistant cancer cell lines. Development of the kt-3000
series is supported, in part, by the St. Baldrick’s Foundation
Martha’s BEST Grant for All, which is aimed at developing new
treatments for Ewing sarcoma, an aggressive bone and soft tissue
cancer in children and young adults.
Rakovina Therapeutics scientific presentations,
including yesterday’s poster from the AACR Special Conference on
Sarcomas can be found on the Company’s website.
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.
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Contact:
Rakovina Therapeutics Inc.David HymanChief
Financial OfficerEmail: info@rakovinatherapeutics.com |
Investor Relations
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