AGM Statement
RNS Number : 8592O
N4 Pharma PLC
30 June 2025
30 June 2025
N4 Pharma plc
("N4 Pharma" or the "Company")
AGM Statement
N4 Pharma plc (AIM: N4P), the UK biotech developing Nuvec®, its proprietary gene delivery system to enable advanced therapies for cancer and other diseases, will hold its Annual General Meeting (AGM) at 11.00 am today at Arch Law Limited Huckletree Bishopsgate, 8 Bishopsgate, London, EC2N 4BQ.
Nigel Theobald, Chief Executive Officer, will provide the following statement:
"As outlined in the Company's final results early this month, I am pleased to report that N4 Pharma continues to deliver strong technical and operational progress, maintaining a clear strategic focus on advancing its Nuvec® RNA delivery platform.
"RNA therapeutics remains a rapidly expanding field of global interest among major pharmaceutical companies and biotech innovators, yet the central challenge persists: how to deliver these therapies safely, effectively, and intact to their target tissues. This is precisely where N4 Pharma believe Nuvec® offers a unique and highly differentiated solution.
"Over the past year, Nuvec® has generated compelling pre-clinical data, consistently meeting key performance benchmarks for next-generation RNA delivery systems. These results reinforce the Company's belief in Nuvec®'s potential to become a delivery platform of choice.
"In May 2025, building on positive data from the Company's first in vivo efficacy study of N4 101 in a standard animal model of Inflammatory Bowel Disease (IBD) and supported by a successful fundraising round in April 2025, N4 Pharma launched an expanded work programme to strengthen the commercial data package around Nuvec®.
"This enhanced programme, to be delivered over the next 12 to 18 months, is being executed by a highly experienced team with deep expertise in both science and commercialisation. It is focused on the following key data packages that are designed to support future deal-making and add significant shareholder value.
| · | Oral delivery- Nuvec® protects SiRNA from degradation, which enables oral delivery to the GI tract. Oral delivery has significant advantages compared with other methods such as intrathecal injections and intravenous infusions, and, as yet, no orally delivered RNA therapeutic has been approved. N4 Pharma will expand the existing data set to demonstrate the performance of an orally delivered RNA therapeutic. |
| · | Endosomal release- getting the RNA into cells is one part of the process; the RNA then has to be released from the delivery vehicle for it to take effect. This is a very inefficient process with existing delivery platforms such as lipid nanoparticles, which typically release only a few per cent of the RNA. The planned work package aims to demonstrate a higher endosomal release for Nuvec® compared with lipid nanoparticles, which should lead to improved RNA delivery into the cytoplasm and increased therapeutic activity. This would be a significant competitive advantage for Nuvec® in the market. |
| · | Dual loading- loading of two RNA therapeutics allows delivery of two drugs in a single 'drug entity', with the potential to deliver more efficacious combination therapies, whilst only requiring a single set of toxic studies. Nuvec® is known to be able to deliver multiple RNA therapeutics, and this work programme aims to build out the existing data to demonstrate this key benefit of the Nuvec® platform. |
| · | CMC (Manufacturing)- it is essential that a delivery platform has class-leading performance as well as being straightforward and reproducible to manufacture. Nuvec® has been shown to be simple to manufacture, and this work package will now focus on improving yield and demonstrating sterile manufacture for human studies, which de-risks future development for a partner. |
| · | Targeting- the RNA to specific cell types or tissues is the holy grail of RNA therapeutics because it reduces off-target effects and improves efficacy. All RNA therapeutics developers would wish to target their drug products to specific tissues. Early work at N4 Pharma has shown that Nuvec® particles can be modified on their surface to target particular cells, and this work package will expand on this critical data set that will set Nuvec® apart from all other delivery platforms. |
| · | Toxicity- existing delivery platforms such as viral vectors and lipid nanoparticles have poor in vivo tolerability profiles. Nuvec® is made of silica, which is known to be benign from a toxicity perspective. This work package will demonstrate good in vivo tolerability in a number of models, which again significantly de-risks future development for a partner. |
| · | Pharmacokinetics and Biodistribution-it is critical that any drug gets to the site of action, remaining there long enough to have a durable effect, and that remaining drug or metabolites are excreted safely. This work package aims to measure, using standard techniques, the behaviour ofNuvec® particles in vivo to demonstrate an appropriate PK profile for RNA drugs. |
| N4 Pharma plc Nigel Theobald, CEO Luke Cairns, Executive Director Submit your questions directly to the management team via the N4 Pharma Investor Hub | Via N4 Pharma Investor Hub:investors.n4pharma.com https://investors.n4pharma.com/link/qy1wAr |
| SP Angel CorporateFinance LLP Nominated Adviser and Joint Broker Matthew Johnson/Jen Clarke (Corporate Finance) Vadim Alexandre/Abigail Wayne/Rob Rees (Corporate Broking) | Tel: +44 (0)20 3470 0470 |
| Turner Pope Investments (TPI) Limited Joint Broker Andy Thacker James Pope | Tel: +44 (0)20 3657 0050 |
| Northstar Communications Limited Investor Relations Sarah Hollins | Tel: +44 (0)113 730 3896 |
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