London-based CHARM Therapeutics has announced a strategic discovery collaboration with Bristol Myers Squibb(NYSE: BMY) for the discovery of new medicines. CHARM will leverage its proprietary deep learning platform, DragonFold, to identify compounds against targets of interest via through protein-ligand co-folding. CHARM is responsible for the early discovery of compounds, and Bristol Myers Squibb may license and develop compounds from the collaboration. As part of the agreement, CHARM will receive an upfront payment and investment in the company, along with additional payments if Bristol Myers Squibb exercises its option to any of the program compounds. CHARM is a 3D deep learning research company with a focus on cancer and other diseases. The company has raised $50 million to date and is supported by investors such as OrbiMed and Khosla Ventures.
Royal Papworth Hospital NHS Foundation Trust has become the first UK hospital to use the CMR Surgical’s Versius Surgical Robotic System in thoracic procedures. The system allows for precision and accuracy in the chest cavity through small incisions between the ribs, and is specifically designed for thoracic surgery. The small and modular design of the system also allows for optimal access through the rib cage. The first cases with Versius at Royal Papworth are scheduled for spring 2023.
London-based RQ Bio and Vancouver-headquartered AbCellera (NASDAQ: ABCL) have entered a strategic collaboration to develop new therapies for up to three infectious diseases, including influenza and cytomegalovirus. By combining RQ Bio's expertise with AbCellera's discovery engine, the partnership aims to provide lasting protection for at-risk patients. Under the agreement, RQ Bio has the right to develop and commercialise the resulting therapeutic antibodies. AbCellera will receive research payments and is eligible for milestone payments and royalties on net sales of products.
Edinburgh-based Macomics and Osaka-based Ono Pharmaceutical have partnered to develop new immuno-oncology antibody drugs against a novel macrophage target in cancer. Macomics will identify and characterise antibody candidates using its ENIGMACTM macrophage drug discovery platform, and Ono will have an exclusive option to license global rights to the candidates for further development and commercialisation. Macomics will receive an up-front payment, R&D funding, and milestone payments, as well as tiered royalties based on global net sales. Macrophages are often the most abundant immune cell in many types of cancer, and modulating TAMs can enhance the body's ability to fight cancer.
Nottingham-based Agility Life Sciences and Barcelona-based Solitek - Solid Technologies SL have formed a strategic partnership to accelerate their clients' pharmaceutical development milestones. The partnership includes the promotion of each other's services, providing training, technical support, and client liaison. This mutually beneficial partnership will strengthen both companies' client base.
London-based Complement Therapeutics (CTx) and Liverpool-based Pharmaron have partnered to develop and manufacture CTx001, a gene therapy for the treatment of late dry age-related macular degeneration (Geographic Atrophy, GA). CTx001 is currently in pre-clinical development as an Adeno Associated Virus (AAV) based gene therapy. Pharmaron's facilities and expertise will help deliver clinical-grade drug products for first-in-human clinical trials set to commence in H2 2024. The partnership aims to bring CTx001 through clinical proof of concept .
Oxford-based Grey Wolf Therapeutics has dosed the first patient in the initial monotherapy module of an adaptive Phase 1/2 clinical trial evaluating GRWD5769. GRWD5769 is the company’s investigational first-in-class ERAP1 inhibitor. The trial is designed to evaluate the safety, tolerability, preliminary efficacy, and pharmacokinetics of GRWD5769 alone and in combination with Regeneron’s PD-1 inhibitor Libtayo in patients with advanced solid tumors. The company’s therapeutic strategy (targeted cancer neoantigen creation) is focused on inhibiting the endoplasmic reticulum aminopeptidases (ERAP1 or ERAP2), which play a key role in the antigen presentation pathway. The inhibition results in the mobilisation of an entirely novel T cell response against the tumor that increases tumor visibility where current therapies are ineffective.
The UK Medicines and Healthcare products Regulatory Agency’s Stem Cell Bank is testing a new robot that grows stem cells, called the CellQualiaTM Intelligent Cell Processing System. Due to manufacturing challenges, stem cell-based therapeutics are limited in availability. The CellQualiaTM system being tested at the MHRA has the potential to change this. It is being trialled over a 12-month period to see whether the cells produced by the fully automated Intelligent Cell Processing System meet the standards needed for them to be used in the manufacture of potentially life-saving treatments. The trial is part of a UK-based international research programme, launched in 2021, and a partnership between the MHRA, SAKARTA, and Sinfonia Technology Co. Ltd, supported by Kobe-based Foundation for Biomedical Research and Innovation.
London-based LIfT BioSciences has released pre-clinical data showing that its Immunomodulatory Alpha Neutrophil product (IMANp). Results exhibit both cytotoxic and immunomodulatory functionalities in solid tumour microenvironment. IMANp can recruit and activate the patient's immune system to infiltrate the tumor micro-environment and turn it hot. It can also be used in combination with other therapies where efficacy is limited due to the absence of effector cells in the tumor micro-environment. The company plans to move into clinical trials next year after generating successful functional proof of concept data for iPSC-derived and gene engineered IMANp products.
Genomics England has made significant progress in long-read sequencing, which can spot structural changes in the genome more easily. Researchers have analysed over 100 whole genome sequences using novel Oxford Nanoporesequencing technology, and have proven the concept of building an analytical pipeline for long-read sequencing. This technology will be used alongside existing short-read sequencing to support clinical decisions.
Oxford AHSN has partnered with Caristo Diagnostics on a feasibility study into the CaRi-Heart technology. CaRi-Heart is an AI platform that predicts cardiovascular risk in patients with suspected coronary artery disease (CAD). It uses medical imaging analysis software that measures the perivascular fat attenuation index (FAI) and clinical factors to generate an eight-year cardiac risk estimate. This technology can detect coronary inflammation before artery narrowing has developed, years before a heart attack may occur. The Oxford AHSN conducted a feasibility study on this technology, which evaluated its utility in the NHS care pathway for chest pain management. The technology is undergoing further studies to gain regulatory approval and for adoption by the NHS.
Oxford-based Brainomix has received FDA clearance for its Brainomix360 e-ASPECTS tool for stroke. The AI-powered platform provides real-time interpretation of brain scans to guide treatment decisions. The Brainomix 360 platform uses state-of-the-art AI algorithms to assess non-contrast CT scans and automatically generate an ASPECTS score. The score is used to determine the best course of treatment for stroke patients. Recent studies have shown that Brainomix software reduces door-in-door-out times and improves patient outcomes. The technology will now be introduced to stroke centers across the US with support from Brainomix's established field team and Blackford, a pioneering imaging AI platform and solutions provider.
Wales-based Copner Biotech announces the granting of its first patent, GB2605009B, a 3D printing method that manufactures its cell scaffold product. This patent protects the novel way in which cell scaffolds are constructed by 3D printing, providing a suitable structure for cell growth that mimics in vivo tumour growth. Copner Biotech has several other patents pending.
Cambridge-based PhoreMost and Oxford Drug Design have entered a collaboration agreement on a targeted protein degradation discovery programme for novel cancer therapeutics. The project uses Oxford Drug Design's AI computational platform and PhoreMost's next-generation SITESEEKER phenotypic screening platform and PROTEINi libraries. The goal is to identify and develop new compounds for onward optimisation.
Cambridge-based Minogame has released its ScanXm version 1.0.3. Minogame provides biomedical image analysis software. It now runs supports all modern GPUs, and includes new AI tools for automatic segmentation and identification of vertebrae in CT scans.
Oxford-baed Arctoris has partnered with Synthego to offer researchers a faster and more seamless workflow from CRISPR edit to phenotypic data. The partnership combines expertise in automated CRISPR cell line engineering with Arctoris's automated and machine learning-empowered drug discovery platform to accelerate and scale research.
London-based Pangaea Data has published the capabilities of their AI-driven product in the British Medical Journal Health & Care Informatics. The product can predict ICU length-of-stay and risk of mortality with 85% precision. The company has discovered 22x more undiagnosed, misdiagnosed, and miscoded patients, and halved treatment costs. Pangaea is founded by Dr Vibhor Gupta and Prof Yike Guo, and advised by Lord David Prior, Mr Andy Palmer, and Dr Thomas Dyrberg.
Bellshill-based EnteroBiotix has commenced a Phase 2 clinical trial named 'IMPuLCE' to assess EBX-102 for treating liver cirrhosis and hepatic encephalopathy. EBX-102 is delivered orally and contains diverse full-spectrum microbial ecosystems to restore microbial ecology and target multiple key disease pathways. The trial involves 56 patients with liver cirrhosis across the UK and will evaluate EBX-102 in patients with cirrhosis and hepatic encephalopathy (mortality rate of up to 40% of affected patients) being treated with standard of care medications, including Rifaximin. The trial is an important milestone for EnteroBiotix as it advances a new class of full-spectrum microbiome drug through the clinic.
Cardiff-based CatSci has unveiled its oligonucleotides capability. It will be led by Dr Nigel Richardson (Director, New Modalities). CAtSci has over 40 years of oligonucleotide research, development and manufacturing. The company provides enabling technologies and work with preferred partners to create affordable, best-in-class small molecule therapeutics. CatSci has recently received several awards for their work, including the Queen's Award for Enterprise: International Trade 2022.
Nottingham-based Source Genomics has become the first UK-based provider to offer Olink Proteomics services for proteomics and high-throughput biomarker discovery.
Cambridge-based Isogenica and the Frederick National Laboratory for Cancer Research have announced the start of two more projects as part of their contractual relationship. The aim of the multi-project contract is to develop molecules that can be used in clinical laboratory assays to measure biomarkers correlated with the effectiveness of cancer immuno-oncology agents. To that purpose, Isogenica will develop and optimise VHH and antibody candidates.
Birmingham-based Nonacus has launched a non-invasive test called GALEAS Bladder, aiming to detect bladder cancer. The urine-based test provides a highly sensitive and accurate diagnosis, reducing the need for invasive cystoscopies. The test has been developed in collaboration with the University of Birmingham, the test has been validated in over 600 patient samples from 3 UK clinical cohorts. The technology used in GALEAS Bladder offers the potential to reduce the reliance on invasive cystoscopies and expensive imaging for non-muscle-invasive bladder cancer surveillance, as well as hematuria triage.
Manchester-based Monument Therapeutics has announced positive results from its first-in-human Phase I study of MT1980, a novel potential treatment for neuroinflammation. The drug was found in the cerebrospinal fluid of all volunteers, indicating its presence in the brain for each dose level of MT1980. The unique absorption profile of MT1980, achieved using technology developed by TRx Biosciences and exclusively licensed to Monument Tx, resolves blood-brain-barrier penetration limitations that exist with standard on-market formulations of the compound. The company plans a further Phase I clinical study to provide additional safety and pharmacokinetic data following multiple dosing of MT1980, in addition to evidence of an anti-inflammatory effect in the brain.
UK Dementia Research Institute at the University of Cambridge has developed a way to increase levels of the 'cold shock protein' in the brains of mice, protecting them from prion disease. The protein helps protect the brain from damage and allows it to continue to form new connections. The researchers tested antisense oligonucleotides (ASOs) to increase levels of the cold shock protein in the brains of mice – and hence protect them. A single injection with the ASO was sufficient to provide long-lasting protection for these mice, preventing neurodegeneration progression. The work was led by Prof Giovanna Mallucci and funded by Freie Universität Berlin, the Medical Research Council, Alzheimer’s Society and Alzheimer’s Research UK.
Cambridge-based Aila Biotech has signed a patent portfolio option with Babraham Institute to develop a gene delivery treatment for patients with traumatic brain injury and neuroinflammation. Traumatic brain injury can lead to dementia and cognitive disability, but few treatments are available to prevent inflammation in the brain. Pioneering research by Prof Adrian Liston and Dr Mathew Holt enables the delivery of a protein known as interleukin 2 at sites of brain inflammation to stop inflammation and initiate repair. The treatment was protective in mouse models of neuroinflammation, traumatic brain injury, multiple sclerosis, stroke, and cognitive decline with age. Aila Biotech is pursuing venture capital to raise funding for a clinical trial.
Oxford-based Oxford Vacmedix has completed the first part of Phase I trial of OVM-200, its lead cancer vaccine. OVM-200 is a cancer vaccine developed using OVM’s novel recombinant overlapping peptide (ROP) platform, which targets survivin, a protein overexpressed by certain cancer cells. The Phase I trial of OVM-200 is focused on safety and on establishing an immune response in patients with three tumour types – non-small cell lung cancer (NSCLC), prostate cancer, and ovarian cancer. Twelve patients have been treated in Phase 1a, and a further 24 patients will be treated in Phase 1b. Oxford Vacmedix is currently seeking Series B funding to advance OVM-200 to Phase 2 and OVM-100 into Phase 1 trials.