Government imposed stay-at-home orders have posed a challenge to clinical trial sponsors and contract research organizations (CROs) as traditionally, clinical trials revolve around patients’ physical access to investigative sites. An alternative to this is the virtual clinical trials paradigm in which patients are at the center of new medical product development and elements of the process such as screening, visits and data transmission are managed electronically from remote locations.
According to the survey, which was conducted by ERT in April and May, 2020:
- The biggest issue keeping participants up at night is screening for new clinical trials patients (79 percent)
- The primary issues impacting trials over the next six to twelve months are trial management (32 percent) and patient recruitment and enrollment (25 percent)
- The most common ways to collect data in a virtual clinical trial are telehealth (75 percent) and patient-used devices (75 percent)
“There are many benefits to virtual clinical trials,” said Jim Mahon, vice president, Chief Strategy and Marketing officer, ERT. “They are safer and more convenient for patients and more cost-effective for sponsors and CROs. Patient recruitment is easier, drop-out rates are lower, timeframes are shorter, and endpoint data is more accurate. The acceleration we’re seeing in the adoption of virtual clinical trials is a net positive for all stakeholders. It allows for the continuation of critical studies during COVID-19, and more patient-focused and efficient studies post-pandemic. We look forward to witnessing how these powerful technologies impact the availability of life-changing therapies and treatments.”