Redx Pharma plc Presentation of RXC007 Preclinical Efficacy Data
May 11 2023 - 2:00AM
RNS Non-Regulatory
TIDMREDX
Redx Pharma plc
11 May 2023
REDX PHARMA PLC
("Redx" or "the Company")
Redx Presents Preclinical Efficacy Data for RXC007 Showing
Significant Results in Cancer-Associated Fibrosis Models
Alderley Park, UK, 11 May 2023 Redx (AIM:REDX), the
clinical-stage biotechnology company focused on discovering and
developing novel, small molecule, targeted therapeutics for the
treatment of cancer and fibrotic disease announces additional
preclinical data for its lead fibrosis asset, RXC007, and the
Discodin Domain Receptor (DDR)1/2 discovery programme, as presented
yesterday at the Resistant Tumour Microenvironment, Keystone
Symposia, in Vancouver, BC. The data presented were from
preclinical models of pancreatic ductal adenocarcinoma (PDAC) and
triple negative breast cancer (TNBC) , in combination with
chemotherapy and immunotherapy, as current standard of care.
RXC007, in combination with gemcitabine/Abraxane(R) [i] in
metastatic and high-extra cellular matrix (ECM) patient-derived
PDAC models, was shown to increase survival compared to single
agent standard of care alone. The combination of RXC007 with
standard of care provided a significant increase in median survival
days from date of treatment in a dose dependent manner. These new
data on RXC007 complement those also presented at the meeting by
collaboration partner the Garvan Institute of Medical Research
("the Garvan") on REDX10616, a close analogue of RXC007, which were
also presented at the Extracellular Matrix Pharmacology congress
last year. These data show REDX10616, in combination with
FOLFIRINOX, re-sensitised a FOFIRINOX-resistant patient derived
xenograft (PDX) model to treatment and led to a striking increase
in survival in combination with the standard of care triplet
chemotherapy.
Taken together, these data provide a strong rationale for the
potential of ROCK2 inhibition in combination with standard of care
as a potential treatment for cancer-associated fibrosis. Redx plans
to further investigate this treatment setting with the Company's
next-generation ROCK2 inhibitor, RXC007, in the clinic.
Additionally, at the Keystone Symposia, further data were also
presented from Redx's DDR1/2 programme in combination with
anti-PD-1 in TNBC models. Using a tool DDR1/2 inhibitor, in
combination with anti-PD-1, in the TNBC E0771 model resulted in a
statistically significant increase in survival when compared to the
control group, an effect not observed with either single agent
alone.
Caroline Phillips, Senior Vice President Biology, Redx Pharma
commented: "These data, presented in hard-to-treat preclinical
models, highlights the multiple opportunities for our lead asset
RXC007. RXC007 is a highly selective, next-generation, ROCK2
inhibitor, currently in Phase 2a clinical studies for IPF, which
has shown significant potential in other disease areas that we are
excited to pursue in the future. Taken together with the data from
our DDR1/2 programme currently in lead optimization, this provides
support for new mechanisms to provide treatments for
cancer-associated fibrosis which has been associated with poor
prognosis in several cancers."
For further information,
please contact:
Redx Pharma Plc T: +44 (0)1625
UK Headquarters 469 918
Caitlin Pearson, Head of Communications
ir@redxpharma.com
Lisa Anson, Chief Executive
Officer
US Office
Peter Collum, Chief Financial
Officer
SPARK Advisory Partners (Nominated T: +44 (0)203
Adviser) 368 3550
Matt Davis/ Adam Dawes
WG Partners LLP (Joint Broker) T: +44 (0)203
705 9330
Claes Spång/ Satheesh Nadarajah/
David Wilson
Panmure Gordon (UK) Limited T: +44 (0)207
(Joint Broker) 886 2500
Rupert Dearden/ Freddy Crossley/
Emma Earl
FTI Consulting T: +44 (0)203
727 1000
Simon Conway/ Ciara Martin
About Redx Pharma Plc
Redx Pharma (AIM: REDX) is a clinical-stage biotechnology
company focused on the discovery and development of novel, small
molecule, targeted therapeutics for the treatment of cancer and
fibrotic disease and the emerging area of cancer-associated
fibrosis, aiming initially to progress them to clinical proof of
concept before evaluating options for further development and
potential value creation. The Company's lead fibrosis product
candidate, the selective ROCK2 inhibitor RXC007, is in development
for interstitial lung disease being evaluated in a Phase 2a trial
for idiopathic pulmonary fibrosis (IPF) with topline data expected
in Q1 2024. Redx's lead oncology product candidate, the Porcupine
inhibitor RXC004, being developed as a targeted treatment for
Wnt-ligand dependent cancers, is expected to report Phase 2 data in
combination with anti-PD-1 by end 2023. Redx's third drug
candidate, RXC008, a GI-targeted ROCK inhibitor for the treatment
of fibrostenotic Crohn's disease, is progressing towards a CTA
application in H2 2023.
The Company has a strong track record of discovering new drug
candidates through its core strengths in medicinal chemistry and
translational science, enabling the Company to discover and develop
differentiated therapeutics against biologically or clinically
validated targets. The Company's accomplishments are evidenced not
only by its two wholly-owned clinical-stage product candidates and
rapidly expanding pipeline, but also by its strategic transactions,
including the sale of pirtobrutinib (RXC005, LOXO-305), a
non-covalent (reversible) BTK inhibitor now approved by the US FDA
for adult patients with mantle cell lymphoma previously treated
with a covalent BTK inhibitor, and AZD5055/RXC006, a Porcupine
inhibitor targeting fibrotic diseases including IPF, which
AstraZeneca is progressing in a Phase 1 clinical study. In
addition, Redx has forged collaborations with Jazz Pharmaceuticals,
which includes JZP815, a pan-RAF inhibitor developed by Redx which
Jazz is now progressing through Phase 1 clinical studies, and an
early stage oncology research collaboration.
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[i] ABRAXANE (R) is a registered trademark of Abraxis
BioScience, LLC, a Bristol-Myers Squibb Company.
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