New era in virus testing at Canary Wharf

Between J.P. Morgan’s London headquarters and the Mastercard office in Canary Wharf lies an unassuming building that is home to some of the most transmissible viruses known to science. This is where hVIVO, a contract research organisation, conducts human challenge studies for respiratory and infectious diseases. These studies, which gained prominence during the Covid-19 pandemic, involve small groups of volunteers being intentionally infected with a virus to test potential vaccine and drug candidates in the early stages of development.

The new hVIVO facilities in Canary Wharf represent a significant advancement in testing therapeutic candidates. With over 80 studies completed, including the first for SARS-CoV-2, hVIVO aids pharmaceutical companies and biotechs in evaluating early-stage candidates before embarking on large-scale clinical trials, which are both time-consuming and costly.

As climate change and urbanisation increase, the prevalence of infectious diseases is expected to rise. For instance, warmer temperatures could spread mosquito-borne viruses like Dengue fever to regions beyond the tropics.

At an investor’s day event, hVIVO’s CEO Dr Yamin Khan emphasised the unique location of their new facility in Canary Wharf, an area typically associated with finance rather than science. This move aligns with Canary Wharf Group’s vision to establish the area as a European hub for life sciences. The group is already attracting companies to a new 23-storey, 823,000ft² building, aiming to transform the area into a life sciences centre.

For hVIVO, the new facility will enhance the efficiency of their human challenge studies. Volunteers willing to be infected with diseases will stay in state-of-the-art private rooms, equipped with PlayStation 5s and TVs, overlooking the high-rises of Canary Wharf. Meanwhile, hVIVO scientists will work in laboratories equipped with the latest PCR machines and other advanced devices.

The company, focusing primarily on influenza and respiratory syncytial virus (RSV) inoculations, has implemented stringent security measures due to the high-risk biological agents it stores. This is a stark contrast to the neighbouring financial institutions.

hVIVO’s participant recruitment, branded as FluCamp, has gained significant attention online, particularly on TikTok, where videos from enrolled members have garnered around 16 million views. One popular video advertises, “Earn £3,000 with me at FluCamp.”

The benefits of human challenge studies are clear, providing scientific data on dosing, safety, and efficacy, and helping to de-risk later-stage trial data. Additionally, they offer clinical efficiencies by not relying on viral seasons. Professor Stephen Gordon from the Liverpool School of Tropical Medicine highlighted that the UK is a leader in human challenge trials. The UK and Europe play crucial roles in researching infectious diseases, especially compared to the more restrictive US regulatory frameworks. Human challenge studies can lead to financial savings and regulatory advantages, such as fast tracks or breakthrough designations. These studies are poised to be instrumental in combating future epidemic viruses, termed “Disease X” by the World Health Organization.

hVIVO’s new facility at Canary Wharf marks a significant step forward in the field of infectious disease research, combining cutting-edge technology with strategic location to enhance the efficiency and impact of human challenge studies.

Click to view all articles for the EPIC:
Or click to view the full company profile:
    Facebook
    X
    LinkedIn
    hVIVO plc

    More articles like this

    hVIVO plc

    Clinical trial eligibility: Pre-screening and Screening

    In clinical trials, ensuring patient safety is paramount, and researchers must identify suitable participants who meet specific requirements. To this end, there are distinct processes involved, known as pre-screening and screening, which help determine whether a

    hVIVO plc

    Connecting Airway Epithelial Cell Models with Human Challenge Studies

    Airway epithelial cells cultured in Air–Liquid Interface (ALI) conditions provide an environment that closely resembles the human airway system. This method facilitates improved oxygen availability and supports cellular differentiation, replicating the physiological conditions of the human

    hVIVO plc

    Esmée shares her FluCamp clinical trial volunteer experience

    hVIVO plc (formerly Open Orphan plc), led by Cathal Friel, is a rapidly growing specialist contract research organisation (CRO) and the world leader in testing infectious and respiratory disease vaccines and antivirals using human challenge clinical trials,

    hVIVO plc

    Overcoming challenges in high-growth regulated industries

    The Navigating Risk podcast recently explored the challenges faced by high-growth businesses operating in highly regulated industries, particularly life sciences. Helen Yates, the Editor of Global Thought Leadership, engaged in a conversation with Mo Khan, the

    hVIVO plc

    Take a 360° interactive tour of a FluCamp Volunteer Room

    hVIVO plc (formerly Open Orphan plc), led by Cathal Friel, is a rapidly growing specialist contract research organisation (CRO) and the world leader in testing infectious and respiratory disease vaccines and antivirals using human challenge clinical trials,

    hVIVO plc

    Clinical trial approval process in the UK

    The process of obtaining approval for clinical trials is comprehensive, as it involves multiple regulatory bodies that ensure the safety and efficacy of the medical interventions being tested. Researchers begin by meticulously planning the trial, outlining

    hVIVO plc

    hVIVO reports positive results from RSV antiviral human challenge trial

    hVIVO plc (LON:HVO), a fast-growing specialist contract research organisation (CRO) and world leader in testing infectious and respiratory disease products using human challenge clinical trials, has noted the announcement by Enanta Pharmaceuticals, reporting positive topline results from

    hVIVO plc

    The importance of Clinical Trial Monitoring

    Monitoring is essential from the moment a clinical trial is planned until it concludes. This ensures that the study remains unbiased, patient safety is prioritised, and accurate results are achieved. The process of clinical trial monitoring

    hVIVO plc

    The future of vaccine development through human challenge trials

    Testing new treatments and vaccines often requires years, if not decades, to gather sufficient data. In response, scientists are turning to a more direct approach that involves deliberately infecting volunteers with potentially deadly pathogens. A notable

    hVIVO plc

    The impact of Clinical Trial results on medical advancements

    Clinical trials play a pivotal role in advancing the medical industry by allowing new treatments and interventions to be rigorously tested for both effectiveness and safety. Understanding how clinical trial data is used is essential to

    hVIVO plc

    Hvivo reports significant growth in earnings and revenue

    Hvivo, previously known as Open Orphan, saw a significant increase in earnings during the first six months of the year, marking a 67.6% rise. Earnings before interest, taxes, depreciation, and amortisation reached £8.7 million (€10.32 million),

    hVIVO plc

    hVIVO reports strong first half, delivering record revenues and margins

    hVIVO plc (LON:HVO), a fast-growing specialist contract research organisation (CRO) and world leader in testing infectious and respiratory disease products using human challenge clinical trials, has announced its unaudited interim results for the six-month period ended 30 June 2024.

    hVIVO plc

    hVIVO expands to cutting-edge facility in Canary Wharf

    hVIVO plc, a specialist contract research organisation (CRO), is experiencing rapid growth, establishing itself as the global leader in testing vaccines and therapeutics for infectious and respiratory diseases. By conducting human challenge clinical trials, the company