While COVID-19 may be the most prominent example, the 21st century has seen the emergence of many infectious diseases that have significantly threatened human health, including zika, chikungunya and severe acute respiratory syndrome (SARS). With this high incidence of emerging infectious diseases (EIDs) likely to continue, adequately preparing to respond to outbreaks becomes imperative.
One of the most powerful tools in the arsenal against infectious disease is vaccination. While it may not be possible to predict the nature of future epidemics, pre-emptive vaccine research can play a significant role in improving our ability to create effective vaccines quickly. With measures such as vaccine development for high risk EIDs, universal vaccines and versatile vaccine platforms, the medical community will be better prepared to respond to future epidemics.
High-risk EID research
In many cases, such as with COVID-19, outbreaks of novel diseases are related to already-known pathogens. Additionally, previously identified infectious diseases have the potential to increase in incidence or geographic range, as has happened in the past with Ebola. With this knowledge, it becomes clear that research related to known high-risk infectious diseases is invaluable to controlling EID outbreaks. In fact, the World Health Organisation has compiled a list to prioritise the research of diseases that pose the greatest health risk, as determined by epidemic potential and lack of sufficient countermeasures.1
Universal vaccines
In January of 2022, a group of professionals from the National Institute of Allergy and Infectious Diseases, including Dr. Anthony Fauci, penned an article about the urgent need for universal coronavirus vaccines.2 In it, they cited the recent emergence of multiple deadly coronaviruses, and the likelihood of future similar emergences.
Universal vaccines protect against all viruses within a given family — meaning that a universal coronavirus vaccine would not only provide immunity against all known coronaviruses, such as COVID-19 or SARS, but theoretically also coronaviruses that have not yet infected humans. While researchers have not yet achieved an effective universal vaccine of any kind, the ability to protect against illness from specific families of disease that have proven harmful to human health would be highly significant in the prevention of future outbreaks of related EIDs.
Vaccine technology
Advancing versatile vaccine technology can also speed the development of vaccines in the case of an EID outbreak. Long established forms of vaccination, such as deactivated or live attenuated viruses, are not tenable in the event of an emergent disease, in part because of how long it would take to cultivate the required quantities of the pathogen in question.
Newer types of vaccine platforms, however, enable much faster and more versatile vaccine development. Platforms, such as mRNA and viral vectors, only require the genetic code from a new disease to develop an effective vaccine, creating a faster and easier-to-produce option. And new platforms are still being pioneered — for example, researchers at Harvard have demonstrated proof-of-concept for the use of extracellular vesicles (tiny particles that transport molecules between cells in the body) as a vaccination method.3 Continuing to advance vaccine technology will serve to facilitate swifter, more effective EID response.
Looking to the future
Preemptive vaccine research is critical to preparedness against the next EID outbreak.
Disease X, the placeholder name given to the unknown virus that may pose a threat to human health, is always on the horizon. The faster and better researchers can create effective vaccines whenever and wherever new viruses emerge, the more lives will be saved.
For more about fortifying vaccine infrastructure against future epidemics, read the whitepaper.
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Digital Disruption
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Clinical strategies to optimise SaMD for treating mental health
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Digital Disruption: Surveying the industry's evolving landscape
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Clinical trial data anonymisation and data sharing
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Clinical Trial Tokenisation
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Closing the evidence gap: The value of digital health technologies in supporting drug reimbursement decisions
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Digital disruption in biopharma
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Disruptive Innovation
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Personalising Digital Health
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The triad of trust: Navigating real-world healthcare data integration
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Clinical strategies to optimise SaMD for treating mental health
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Patient Centricity
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Agile Clinical Monitoring
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Capturing the voice of the patient in clinical trials
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Charting the Managed Access Program Landscape
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Developing Nurse-Centric Medical Communications
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A guide to safety data migrations
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Outsourced Pharmacovigilance Affiliate Solution
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The evolution of the Pharmacovigilance System Master File: Benefits, challenges, and opportunities
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Sponsor and CRO pharmacovigilance and safety alliances
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Understanding the Periodic Benefit-Risk Evaluation Report
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A guide to safety data migrations
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Patient Voice Survey - Decentralised and Hybrid Trials
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Reimagining Patient-Centricity with the Internet of Medical Things (IoMT)
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Using longitudinal qualitative research to capture the patient voice
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Agile Clinical Monitoring
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Regulatory Intelligence
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An innovative approach to rare disease clinical development
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Using innovative tools and lean writing processes to accelerate regulatory document writing
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Current overview of data sharing within clinical trial transparency
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Global Agency Meetings: A collaborative approach to drug development
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Keeping the end in mind: key considerations for creating plain language summaries
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Navigating orphan drug development from early phase to marketing authorisation
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Procedural and regulatory know-how for China biotechs in the EU
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RACE for Children Act
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Early engagement and regulatory considerations for biotech
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Regulatory Intelligence Newsletter
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Crossing the finish line: Why effective participation support strategy is critical to trial efficiency and success in rare diseases
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Leveraging historical data for use in rare disease trials
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Natural history studies to improve drug development in rare diseases
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Patient Centricity in Orphan Drug Development
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The key to remarkable rare disease registries
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Therapeutic spotlight: Precision medicine considerations in rare diseases
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Advanced therapies for rare diseases
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Transforming Trials
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Ensuring the validity of clinical outcomes assessment (COA) data: The value of rater training
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Decentralised clinical trials
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Biopharma perspective: the promise of decentralised models and diversity in clinical trials
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Decentralised and Hybrid clinical trials
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Practical considerations in transitioning to hybrid or decentralised clinical trials
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Navigating the regulatory labyrinth of technology in decentralised clinical trials
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Biopharma perspective: the promise of decentralised models and diversity in clinical trials
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Implications of COVID-19 on statistical design and analyses of clinical studies
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Increasing Complexity and Declining ROI in Drug Development
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Navigating the Challenges and Opportunities of Value Based Healthcare
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Payer Reliance on ICER and Perceptions on Value Based Pricing
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Payers Perspectives on Digital Therapeutics
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RWE Generation Cross Sectional Studies and Medical Chart Review
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Survey results: How to engage healthcare decision-makers
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Strategies for commercialising oncology treatments for young adults
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