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RNS Number : 2566E Redx Pharma plc 27 October 2022
REDX PHARMA PLC
("Redx" or "the Company")
Redx to Present Poster on Preclinical Efficacy of a Novel, Selective Discoidin
Domain Receptor 1 Inhibitor at the American Society of Nephrology Kidney Week
Alderley Park, UK, 27 October 2022 Redx (AIM:REDX), the clinical-stage
biotechnology company focused on discovering and developing novel, small
molecule, highly targeted therapeutics for the treatment of cancer and
fibrotic disease, today announces it will present a poster on its novel
preclinical Discoidin Domain Receptor 1 (DDR1) inhibitor programme at the
American Society of Nephrology (ASN) Kidney Week (3-6 November 2022, Orlando,
Florida).
As announced in January 2022, Redx is developing potent proprietary DDR
inhibitors with drug-like characteristics that are now in lead optimisation.
The poster will present compelling preclinical data on REDX12271, a novel,
potent, selective and orally active DDR1 inhibitor, in chronic kidney disease
models. DDRs are receptor tyrosine kinases containing a discoidin homology
domain in their extracellular region and which act as non-integrin collagen
receptors. There are two DDR receptors, DDR1 and DDR2, and DDR expression is
increased in many fibrotic diseases. DDRs have recently gained traction as new
druggable targets with the potential to treat multiple fibrotic conditions,
including kidney fibrosis. The poster supports the further investigation of
selective inhibition of DDR1 as a potential novel approach for the treatment
of renal fibrosis associated with chronic kidney disease.
Title: REDX12271 is a novel, selective DDR1 inhibitor with the potential to treat
multiple chronic kidney diseases
Poster Board: TH-PO433
Day/Date: Thursday, 3 November 2022
Time: 10:00-12:00
Session name and category: Posters Glomerular Diseases: Inflammation and Fibrosis PO1301
A copy of the poster will be made available on the Company's website
following the presentation
at: https://www.redxpharma.com/scientific-publications/
(https://www.redxpharma.com/scientific-publications/)
About Chronic Kidney Disease
Defined as a persistent abnormality in kidney structure or function (e.g.
glomerular filtration rate GFR <60 mL/min/1.73 m2 or albuminuria ≥30 mg
per 24 hours) for more than 3 months, chronic kidney disease (CKD) affects 8%
to 16% of the population worldwide. CKD is most commonly attributed to
diabetes and hypertension. However, less than 5% of patients with early CKD
report awareness of their disease. Among individuals diagnosed as having CKD,
staging and new risk assessment tools that incorporate GFR and albuminuria can
help guide treatment, monitoring, and referral strategies. While CKD is
progressive, optimal management can slow its progression to end-stage renal
disease (ESRD). This includes cardiovascular risk reduction (e.g., statins and
blood pressure management), treatment of albuminuria (e.g.
angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers
and more recently SGLT2 inhibitors), avoidance of potential nephrotoxins (e.g.
nonsteroidal anti-inflammatory drugs). Renal fibrosis, characterized by
tubulointerstitial fibrosis and glomerulosclerosis, is one the final
manifestations of CKD as it progresses and is associated with high morbidity.
There are currently no approved treatments to address the interstitial
fibrotic component of this disease.(1)
For further information, please contact:
Redx Pharma Plc T: +44 (0)1625 469 918
UK Headquarters
Caitlin Pearson, Head of Communications
ir@redxpharma.com (mailto:ir@redxpharma.com)
Lisa Anson, Chief Executive Officer
US Office
Peter Collum, Chief Financial Officer
SPARK Advisory Partners (Nominated Adviser) T: +44 (0)203 368 3550
Matt Davis/ Adam Dawes
WG Partners LLP (Joint Broker) T: +44 (0)203 705 9330
Claes SpŒng/ Satheesh Nadarajah/ David Wilson
Panmure Gordon (UK) Limited (Joint Broker) T: +44 (0)207 886 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, highly targeted
therapeutics for the treatment of cancer and fibrotic diseases, aiming
initially to progress them to clinical proof of concept before evaluating
options for further development and potential value creation. Redx's lead
oncology product candidate, the Porcupine inhibitor RXC004, commenced a Phase
2 programme in November 2021. The Company's lead fibrosis product candidate,
the selective ROCK2 inhibitor RXC007, is in development for interstitial lung
disease and commenced a Phase 2a trial for idiopathic pulmonary fibrosis
in October 2022. Redx's third drug candidate, RXC008, a GI-targeted ROCK
inhibitor for the treatment of fibrostenotic Crohn's disease, is currently in
pre-IND stage, with Phase 1 clinical studies expected to commence in 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 BTK
inhibitor now in Phase 3 clinical development by Eli Lilly following its
acquisition of Loxo Oncology and AZD5055/RXC006, a Porcupine inhibitor
targeting fibrotic diseases including idiopathic pulmonary fibrosis (IPF),
which AstraZeneca is progressing in a Phase 1 clinical study. In addition,
Redx has forged collaborations with Jazz Pharmaceuticals, which includes
JZP815, a preclinical pan-RAF inhibitor which has received IND clearance from
the US FDA, and an early stage oncology research collaboration.
To subscribe to Email Alerts from Redx, please visit:
www.redxpharma.com/investor-centre/email-alerts/
(1)Taken in part from Chen TK et al; JAMA. 2019 Oct 1; 322(13): 1294Ð1304.
(https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=31573641)
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