Pandemic-Driven Changes in Pharma Here to Stay as New Clinical Trial Models Take Hold
COVID-19 physical distancing requirements forced change in how traditional clinical trials were conducted and a new Informa Pharma and Oracle study shows the industry is not looking back. Of the 251 people surveyed, 84% implemented alternative tactics to continue their existing clinical trials and/or start new trials during the pandemic. Of those respondents, 82% said these approaches had positively impacted their clinical trials overall. Looking to the future, 97% indicated their organization would continue using at least one of these new methods moving forward, leading with remote monitoring and video (eHealth) visits.
The survey, Clinical Trial Management in a Post-Pandemic World, polled participants from biopharmaceutical and medical device companies, as well as CROs involved in the operations and management of clinical trials from July to September 2021. Respondents, who were largely from North America and Europe, with others from APAC and other regions, were asked about changes made to their clinical trials during the pandemic, the effect of these adaptations, and the impact of these changes on the future of clinical trials.
Of the various methods noted, 45% of respondents said they had adopted remote monitoring in their trials during the pandemic, nearly doubling the number of respondents who reported using remote monitoring a year ago. Among the newly adopted methods that companies plan to continue to use post-pandemic, remote monitoring (32%), video visits (28%), electronic health records (24%), and phone visits led the pack (24%).
The most common positive impacts of the alternative approaches adopted during the pandemic included more timely data access (48%), improved flexibility for patients (41%), and increased speed (38%).
When asked about their confidence in the data generated by newly adopted approaches, 92% of respondents stated they were equally or more confident in the data collected from these methods, compared to data collected via pre-pandemic methods. This was a marked change from the 2020 survey when nearly half of respondents said that data reliability and quality (50%) and data collection (45%) were key concerns in adopting decentralized clinical trials. This significant increase in confidence supports the industry’s continued progress towards more decentralized models.
The study also found that improving the patient experience is a priority. Many respondents (61%) believe allowing patients’ choice will have a positive impact on clinical research and well over half (58%) said that their organizations plan to give patients the option to choose how they participate in clinical trials moving forward.
As the shift to decentralized trials continues, survey respondents expect their organizations to continue using hybrid (44%) and fit-for-purpose (42%) models after the pandemic. Of the four models considered—site-based, fit-for-purpose, hybrid, and decentralized—respondents expect the use of the site-based model to decrease the most (24%).
Behind the Buzz: Why Clinical Research Leaders Flock to SCOPE Summit
February 7th 2025In this episode, we meet with Micah Lieberman, Executive Conference Director for SCOPE Summit (Summit for Clinical Ops Executives) at Cambridge Innovation Institute. We will dive deep into the critical role of collaboration within the clinical research ecosystem. How do we bring together diverse stakeholders—sponsors, CROs, clinical trial tech innovators, suppliers, patients, sites, advocacy organizations, investors, and non-profits—to share best practices in trial design, program planning, innovation, and clinical operations? We’ll explore why it’s vital for thought leaders to step beyond their own organizations and learn from others, exchanging ideas that drive advancements in clinical research. Additionally, we’ll discuss the pivotal role of scientific conferences like SCOPE Summit in fostering these essential connections and collaborations, helping shape the future of clinical trials. Join us as we uncover how collective wisdom and cross-industry partnerships are transforming the landscape of clinical research.
Phase III Trial Data Show Subcutaneous Pembrolizumab as Noninferior to IV Keytruda
March 31st 2025Subcutaneous administration of pembrolizumab with chemotherapy demonstrated a nearly 50% reduction in patient chair and treatment room time while maintaining efficacy and safety endpoints compared to intravenous Keytruda.
Reaching Diverse Patient Populations With Personalized Treatment Methods
January 20th 2025Daejin Abidoye, head of solid tumors, oncology development, AbbVie, discusses a number of topics around diversity in clinical research including industry’s greatest challenges in reaching diverse patient populations, personalized treatment methods, recruitment strategies, and more.
