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Redx Pharma Nominates Another Anti-Fibrosis Drug Candidate

Thu, 09th Jan 2020 11:17

(Alliance News) - Drug developer Redx Pharma PLC on Thursday said RXC007 has been nominated as a drug development candidate for the treatment of fibrosis.

RXC007 targets fibrotic diseases like idiopathic pulmonary fibrosis, a potentially life-threatening chronic lung condition. Fibrosis refers to the scarring of connective tissue in the body.

The drug works by inhibiting Rho Associated Coiled-Coil Containing Protein Kinase 2 (ROCK2), an enzyme thought to be key in the development of fibrosis.

Chief Executive Lisa Anson said: "Redx is pleased to be progressing the development of this exciting drug candidate that selectively inhibits ROCK2 as a potential treatment for multiple fibrotic diseases. This is a challenging area of chemistry and the Redx team is proud to deliver another successful drug candidate. We look forward to taking RXC007 into clinical trials in the first half of 2021."

Alderley Edge, Cheshire-based Redx is aiming to begin a phase one study on the drug in the second half of 2021.

Promising pre-clinical data showed Redx's ROCK2 inhibitor programme, which includes RXC006, another drug candidate, has demonstrated "robust anti-fibrotic effects", the company said.

Redx explained: "Specifically, RXC007 met fibrosis endpoints in disease models of liver and lung fibrosis. Furthermore, RXC007's selective inhibition of ROCK2 over other enzyme isoforms should enable a safe cardiovascular profile in patients."

Redx shares were 1.2% lower at 8.15 pence each in London on Thursday morning.

By Eric Cunha; ericcunha@alliancenews.com

Copyright 2020 Alliance News Limited. All Rights Reserved.

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10 Mar 2022 20:31

IN BRIEF: Redx Pharma notes encouraging safety data for RXC007

(Alliance News) Redx Pharma PLC - Cheshire-based cancer and fibrosis drug developer - Says phase 1 data presented at Virtual Interstitial Lung Disease Drug Development summit shows novel anti-fibrotic drug candidate, RXC007, possesses excellent safety and pharmacokinetic profile in both the single and multiple dose phase. No adverse events were observed following single doses of 2-70 milligrams, dosed once or twice in a day and no serious adverse events were observed in the multiple dose phase, dosed at 50mg twice daily for 14 days, with only transient, reversible mild adverse events observed, it says.

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1 Mar 2022 15:59

UK shareholder meetings calendar - next 7 days

Wednesday 2 March 
Ecofin Global Utilities & Infrastructure Trust PLCAGM
Mila Resources PLCAGM
Paragon Banking Group PLCAGM
River & Mercantile UK Micro Cap Investment Co LtdAGM
Thursday 3 March 
Chemring Group PLCAGM
Petro Matad LtdAGM
Zytronic PLCAGM
Friday 4 March 
Asia Strategic Holdings LtdAGM
Challenger Energy Group PLCEGM re equity raise
JPMorgan Russian Securities PLCAGM
Monday 7 March 
Crystal Amber Fund LtdGM re change of investment policy
Tuesday 8 March 
Anglesey Mining PLCGM re delisting
Caretech Holdings PLCAGM
Driver Group PLCAGM
Redx Pharma PLCAGM
Schroder European Real Estate Investment Trust PLCAGM
Shoe Zone PLCAGM
  
Copyright 2022 Alliance News Limited. All Rights Reserved.

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