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BiVictriX Therapeutics
plc
("BiVictriX",
"BiVictriX Therapeutics" or the "Company")
BiVictriX Reports Positive
Initial In Vivo Data from
BVX002 Solid Tumour Programme
· First
in vivo data shared from
BVX002, BiVictriX's lead solid tumour bispecific ADC
programme
· Complete tumour growth inhibition and tumour regressions observed at
well-tolerated doses in a murine model of ovarian
cancer
Alderley Park,
9 September 2024 - BiVictriX Therapeutics plc
(AIM: BVX), a drug discovery and development company applying an
innovative, proprietary approach to develop a new class of highly
selective, next generation cancer therapeutics, bispecific antibody
drug conjugates ("Bi-Cygni® ADCs"), which exhibit superior potency,
whilst reducing treatment-related toxicities, today announces
positive initial in vivo
data for its lead solid tumour programme, BVX002.
The preclinical study is investigating BVX002
in a murine xenograft model of ovarian cancer, using the human cell
line OVCAR-3. Initial data reported highly significant tumour
growth inhibitions across all doses tested, ranging from 78.3% to
>100% (p-value <0.001). Tumour
regressions of up to 63.1% were also observed at the mid and high
doses.
During the study, BVX002 was dosed once weekly,
with a total of four doses given. All doses of BVX002, including
the highest dose tested, were well tolerated in all mice, even with
the drug having target cross-reactivity in mice. Following
completion of the dosing phase, monitoring of tumour volume post
dosing continues. It is noted that the tumours have continued to
shrink in the mid to high dose arms two weeks post treatment
cessation, highlighting the potential durability of BVX002's
anti-cancer effects. This data builds upon the strong preclinical
in vivo efficacy and
safety data previously reported on our most advanced bispecific ADC
asset, BVX001.
BVX002 targets a novel, cancer-specific antigen
pair found to be selectively expressed in a wide range of solid
tumour indications, including cases of ovarian cancer and non-small
cell lung cancer, but is absent from healthy cells. Evidence from
internal data assessing primary patient samples suggests BVX002's
targeted cancer-specific antigen pair may be present in 60-70% of
patients with high grade serous ovarian cancer.
In June 2024, BiVictriX announced the awarding of
a ca.£0.4 million grant from Innovate UK to help support this
preclinical work with BVX002. The Company will use insights from
this study, together with additional planned studies, to file an
Investigational New Drug (IND) Application with the FDA for BVX002
in due course.
Tiffany Thorn, Chief Executive Officer
of BiVictriX Therapeutics plc, commented:
"This first in vivo data
marks the start of what we anticipate being an incredibly exciting
preclinical data package for our lead solid tumour asset, BVX002.
We are highly encouraged by the significance of the anti-tumour
effect delivered by our therapeutic lead in this hard-to-treat
model of ovarian cancer, which showcases the clear benefit of our
proprietary bispecific ADC approach in a solid tumour setting. We
look forward to providing further updates as we expedite the
development of this asset."
Graph 1: Mean Tumour Volume
Over Time for BVX002-treated and Control
Groups
Graph 2:
Bodyweight Change for BVX002-treated and Control
Groups
ENDS
For more
information, please contact:
BiVictriX
Therapeutics plc
Tiffany Thorn, Chief Executive
Officer
Michael Kauffman, Non-Executive
Chairman
|
Email:
info@bivictrix.com
|
SP Angel
Corporate Finance LLP (NOMAD and Broker)
David Hignell, Caroline Rowe (Corporate Finance)
Vadim Alexandre, Rob Rees (Sales and Broking)
|
Tel: +44 (0) 20 3470
0470
|
Panmure
Liberum Limited (Joint Broker) Emma Earl,
Freddy Crossley, Mark Rogers, Rupert Dearden
|
Tel: +44 (0) 20 3100
2000
|
ICR
Consilium
Namrata Taak, Lucy Featherstone, Max Bennett,
Emmalee Hoppe
|
Tel: +44 (0) 20 3709
5700
Email:
Bivictrix@consilium-comms.com
|
About BiVictriX Therapeutics plc
BiVictriX (AIM: BVX) is an emerging
biotechnology company leveraging clinical experience and its
proprietary discovery engine to advance a new class of highly
cancer-selective, next-generation precision cancer therapies in one
of the fastest-growing markets in oncology. BiVictriX's
first-in-class Bi-Cygni® Antibody Drug Conjugates ("Bi-Cygni®ADCs")
combine superior efficacy with substantially improved cancer-selectivity and safety to
provide opportunities for prolonged dosing and greater efficacy in
the clinic. The Company is advancing its
pipeline to deliver the future of cancer care across a broad range
of haematological and solid cancer indications in areas of high
unmet medical need.
Find out more
at www.bivictrix.com and
connect with us on LinkedIn and
Twitter @BiVictriX.