e-therapeutics plc
("e-therapeutics" or "ETX" or the "Company")
Business Update
Proof-of-concept datasets on four assets
Two programs to progress to IND-enabling studies
Range of specialist AI agents in development
2023 was a year of significant execution and progress in e-therapeutics' mission of computing the future of medicine. ETX has moved rapidly to incorporate Large Language Models (LLMs) and transformer technology into its platforms, while continuing to deploy advanced analytics and AI. The Company now has multiple, successful case studies showcasing the power of AI within its drug discovery process combined with the speed and specificity of its GalOmic RNAi drug platform.
A key part of the Company's strategy is to build a highly differentiated therapeutic pipeline, having exclusively nominated and prosecuted novel target genes not pursued by any other RNAi player. These targets were identified in-house, leveraging HepNet's suite of proprietary datasets and advanced analytical functionality.
All nominated targets investigated to date have yielded positive results in preclinical studies. ETX believes that this outstanding hit rate is a result of the unique combination of AI-enhanced computational target selection and drug design coupled with siRNA, a well-tolerated and highly specific modality. The Company is confident that these datasets will be of significant interest to prospective partners and is actively exploring potential partnerships. Pipeline highlights include:
- ETX-407 for the treatment of dry age-related macular degeneration (dAMD), a leading cause of blindness worldwide, has the potential to be a transformative, patient-friendly (no intravitreal injections required) therapeutic option with human genetic validation. ETX-407 demonstrates the applicability of ETX's hepatocyte-targeting GalOmic platform to indications affecting distal organs. In dAMD, the ability to modulate disease pathology without direct injection into the eye and with infrequent administration (at least monthly) is a material differentiator from available treatments.
Non-human primate data readouts for this target were produced in just 9 months after target nomination, demonstrating ETX's ability to go rapidly from "idea" to in vivo results at a pace not achievable by other drug modalities.
- ETX-312 has shown exceptional results in an industry-leading diet-induced obesity (DIO) model of NASH/MASH1. The model, developed by Danish company Gubra, is rated by experts as the most translatable murine model of NASH/MASH. ETX-312 was assessed both as monotherapy and as a combination treatment, including with GLP-1 receptor agonists. The disease modulation seen with ETX-312's highly novel approach is considered extremely significant in the context of the approved and emerging NASH/MASH treatment landscape.
- IND/CTA enabling studies for both ETX-407 and ETX-312 are to commence in due course.
- Preclinical studies for ETX-148 as a treatment for haemophilia have been successfully completed. ETX-148 demonstrated protection from joint bleeds in mouse models of haemophilia with no thrombotic risk, thereby addressing a key unmet need in haemophilia of reducing haemarthrosis (joint bleeds) with a low treatment burden.
- Preclinical studies of ETX-291 for the treatment of cardiometabolic disease have been successfully completed. In a representative disease model, ETX-291 impacted multiple cardiometabolic disease drivers resulting in a pleiotropic benefit and highlighting its potential to treat a broad range of cardiometabolic indications.
- Continued progress on ETX-258 in an undisclosed indication.
- Last near-term milestone successfully achieved in collaboration with iTeos in immuno-oncology, validating the Company's computational approach to modelling human biology and identifying novel potential targets. This successful partnership with iTeos provides additional evidence of the power of ETX's computational approaches to drug discovery. The Company is also eligible to receive further undisclosed milestones.
The Company expects to end the year with a strong balance sheet with a cash position of c.
1 Nonalcoholic steatohepatitis (NASH) is now known as metabolic dysfunction-associated steatohepatitis (MASH) following a recent change in disease nomenclature.
Ali Mortazavi, Chief Executive Officer of e-therapeutics, commented: "Against the backdrop of the harshest macroeconomic and sector conditions seen in decades, 2023 was a year of remarkable progress for e-therapeutics. We now have compelling evidence demonstrating the applicability of our computational/AI systems across our business. We have reproducibly and rapidly progressed multiple programs from novel target discovery to strong in vivo proof-of-concept, with an outstanding hit rate. This has all been achieved with a rigorous eye on our costs and maintaining a healthy balance sheet.
"Both ETX-407 and ETX-312 have the potential to be highly differentiated, first-on-target medicines in diseases with high unmet need and we are excited to be progressing these assets towards the clinic. ETX is now firmly established as a leader in the emergent TechBio sector, and we look forward to 2024 with great confidence."
The information contained within this announcement is deemed by the Company to constitute inside information as stipulated under the Market Abuse Regulations (EU) No. 596/2014 ('MAR') which has been incorporated into
Enquiries
e-therapeutics plc |
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Ali Mortazavi, CEO Timothy Bretherton, CFO
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Tel: +44 (0)1993 883 125 www.etherapeutics.co.uk |
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SP Angel Corporate Finance LLP |
Tel: +44(0)20 3470 0470 |
Nominated Adviser and Broker |
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Matthew Johnson/Caroline Rowe (Corporate Finance) |
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Vadim Alexandre/Rob Rees (Corporate Broking) |
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About e-therapeutics plc
e-therapeutics plc ("ETX") integrates computational power and biology information to discover life-transforming RNAi medicines. The Company's technology uses computation to capture and model human biology, identify novel targets, and develop RNAi medicines against those targets that can be rapidly progressed to the clinic.
ETX's proprietary HepNet™ platform enables the generation and analysis of biological network models, providing a novel and mechanistic approach to drug discovery. This approach explicitly considers the true complexity of biology to make more reliable predictions from large complex data sets and ETX's proprietary hepatocyte knowledgebase - the world's most comprehensive and integrated hepatocyte-centric data resource. The Company generates, prioritises, and tests millions of hypotheses in silico to identify better therapeutic targets with higher confidence.
GalOmic™, ETX's proprietary RNAi platform, enables targeted delivery to hepatocytes in the liver and the specific silencing of novel disease-associated genes, identified by HepNet™. The focus on hepatocytes offers the opportunity to tackle a wide variety of diseases. The liver is a highly metabolically active organ which performs a key role in many biological processes and vital functions crucial for human health. ETX's GalOmic™ constructs have demonstrated compelling in vivo performance in terms of depth of gene silencing and duration of action.
The Company is progressing a pipeline of first-in-class RNAi candidates across a variety of therapeutic areas with high unmet need, including preclinical programs in cardiometabolic and metabolic diseases, haemophilia, and other undisclosed indications. ETX has also partnered with biopharma companies such as Novo Nordisk, Galapagos NV and iTeos Therapeutics using its computational network biology approach across a diverse range of drug discovery projects.
The Company is based in London, UK and listed on the Alternative Investment Market of the London Stock Exchange ("AIM"), with ticker symbol ETX.
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