ICON is currently working on several COVID-19 treatment and vaccine trials.
We have conducted more than 246 vaccine studies globally, including over 40 studies in respiratory viruses, within the past five years alone. In February ICON quickly mobilized its Vaccines, Infectious Diseases and Government and Public Health Solutions resources to assist both government and commercial clients in addressing the COVID-19 global threat and is already providing clinical monitoring and safety oversight on a number of new COVID-19 trials. ICON is a preferred partner for BARDA and has participated in seven studies during infectious disease outbreaks within the past 10 years, including two for H1N1 during a H1N1 pandemic and three for H7N9.Download factsheet
In this whitepaper, ‘Pandemic respiratory vaccine clinical trials: A departure from business as usual’, we focus on the corresponding success factors that can keep pandemic respiratory vaccine trials running at optimal speed and efficiency.Read the whitepaper
In this webinar, industry experts presented regulatory and operational insights to that enable you to be proactive now to protect patient safety and minimize disruption.Watch webinar recording now
ICON has considerable experience in supporting trials of respiratory disease, infectious disease affecting respiratory function, and supporting investigational treatment. Additionally, our Medical Device & Diagnostic experts have conducted studies to aid in the diagnosis of respiratory conditions or with devices utilised to administer drugs in support of respiratory conditions.
As the COVID-19 pandemic evolves affecting the regulatory and clinical and landscape, ICON experts are available to support all aspects of your respiratory programme requirements.
Webinar: 11 June - Navigating the “new normal” during COVID-19: A regulatory and clinical perspective for medical devices - register nowDownload factsheet
ICON is working on several COVID-19 clinical trials. Download the following case studies:
COVID-19 Vaccine study: (PDF) One client trial investigating a prophylactic vaccine study in healthy participants required rapid patient recruitment, site selection, and study start-up.
COVID-19 - Easing the regulatory burden: (PDF) Various regulatory agencies have all published new recommendations on how to manage clinical trials in the wake of the COVID-19 pandemic. To accelerate the development of COVID-19 treatments and vaccines in general, institutional review boards, ethics committees and regulatory authorities are expediting timelines. Where ICON has encountered countries that have not implemented expedited review times, we have reached out directly to ensure this is implemented.
COVID-19 Treatment: (PDF) One client trial investigating an antiviral treatment for patients with conﬁrmed coronavirus infection required rapid patient recruitment, site selection, and study start-up across multiple geographies.
Over the past decade, researchers have made great strides in vaccine research with gene sequencing, further development of mRNA and DNA vaccine platforms, and novel adjuvants for more traditional antigen based products. These advancements have enabled biopharmaceutical and government entities to respond to infectious disease outbreaks by fast tracking both vaccines and treatments in record time.
In the current pandemic, regulatory agencies such as the FDA and EMA and have expedited commercial approvals to bring safe vaccines and treatments to market. Groups such as CEPI and BARDA have enabled key assets and infrastructures to be leveraged in response to this pandemic.
However, numerous key development challenges to delivering a coronavirus vaccine remain.
Related blog: COVID-19 vaccine trials
Related media article: Cindy Dukes, VP Vaccines at ICON, features in an MIT Technology Review article 'Here’s what we have to do to show a coronavirus vaccine works'Read full article
Cyber attacks have increased dramatically during the COVID-19 pandemic. Opportunistic cyber criminals can use the current pandemic to steal intellectual property and patient information.
The pandemic is affecting how clinical trials are managed, not just in terms of patient recruitment and immediate patient care but also in terms of data collection, analysis and safety reporting.
For IVD manufacturers, the emergence of a novel virus is challenging as the detection of such viruses require quickly developed, novel diagnostic solutions.
The success factors that can keep pandemic respiratory vaccine trials running at optimal speed and efficiency.
Need for rapid diagnostic testing to identify and track people infected by or exposed to coronavirus.
A dynamic market and evolving regulations.
Adapting clinical trial protocols can help to keep participants enrolled and receiving treatments and assessments.
Impact of COVID-19 pandemic.
Patients with cardiovascular disease are particularly susceptible to respiratory infections.
A look at the potential impact of Coronavirus.
The ICON Coronavirus Observatory applies powerful AI analysis and data visualisation to COVID-19 clinical trials news and social media, providing updates on the latest clinical trials, with insights into trending topics driving Coronavirus reporting. The Coronavirus Observatory also breaks down the global impact of the virus, looks at trending topics per country, and highlights important perspectives from the key organisations, including non-governmental organisations, public health authorities and the medical science community.
Download: Quick guide to the ICON Coronavirus Observatory (PDF)Visit Coronavirus Observatory