Lessons Learned from COVID-19 Vaccine Trials

28 April 2022 | Thursday | News

A CRO perspective on accelerating clinical development
Image Source : Public Domain

Image Source : Public Domain



IQVIA Institute releases report on Lessons Learned from COVID-19 Vaccine Trials

Lessons Learned from COVID-19 Vaccine Trials
A CRO perspective on accelerating clinical development
The COVID-19 viral pandemic has led to more than 500 million infections and 6.2 million deaths worldwide by mid-April 2022 and has been one of the top three causes of death in the United States since March 2020. The unprecedented modern-day global need for rapid development of effective vaccine and therapeutic solutions was met by a massive and coordinated response across critical health system stakeholders and led to the development of COVID-19 vaccines in well under a year — timelines previously unheard of in vaccine clinical development.
The research behind this report – Lessons Learned from COVID-19 Vaccine Trials – explores model changes that allowed for clinical trial efficiencies from the perspective of the CRO and is based on a set of workshops with COVID-19 vaccine clinical delivery teams. Our emphasis is on understanding what was possible because of the drastic operating environment changes and assessing what can be carried forward into the post-pandemic clinical development pipeline of therapies for other illnesses.
Key findings:
  • COVID-19 vaccines were available for public use in seven months from the start of clinical trials in a record-breaking, cross-stakeholder response to the urgent, unmet need driven by rapidly spreading unchecked viral infections.
  • Environmental enablers, including more than $20Bn in public-private funding, regulatory authority focus, and historic investigator and subject interest in trial participation were critical in delivering these vaccines, thanks to a shifted risk-return balance.
  • A CRO explicit analysis of the operational drivers of trial-specific time savings showed pivotal trials led to an EUA filing with a 26-month, or 70%, savings versus historic trials as a result of operational improvements, organizational responses, and clinical development model improvements.
  • Process improvements driven by innovation and resource focus in contracting, start-up, recruiting and database lock were supported by intensive team, governance, and leadership focus.  All of the operational and organizational changes could be tracked back to a blended shift in process redesign, resource utilization, decision-making practices, and partnership behaviors.
  • ROI analysis highlights a set of changes that are high efficiencies with potential to drive value going forward if implemented beyond vaccine trials, and a second set that is more investment intensive, but includes important drivers of speed for consideration on larger scale or highly time-sensitive trials.
Learn more by downloading the report and graphic exhibits at iqviainstitute.org. As always, I invite you to join the conversation about this important topic and more on LinkedIn and Twitter. And get the latest news from the Institute by joining our mailing list.
Murray Aitken
Executive Director
IQVIA Institute for Human Data Science
The study was produced independently by the IQVIA Institute for Human Data Science as a public service, without industry or government funding. 
© 2022 IQVIA. All rights reserved.
Contact us at iqvia.com
4820 Emperor Boulevard, Durham, NC 27703, USA


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