University of Maryland Researchers to Develop Devices to Revolutionize Drug Research
COLLEGE PARK, MD, September 18, 2007-A multi-disciplinary group of researchers from the University of Maryland, College Park, and the University of Maryland Biotechnology Institute (UMBI) has won a competitive, $2 million National Science Foundation (NSF) grant to revolutionize the way researchers develop and test pharmaceutical drugs.
The group, led by William Bentley, Herbert Rabin Distinguished Professor and chair of the Fischell Department of Bioengineering at the University of Maryland’s A. James Clark School of Engineering, plans to build devices that test new drugs using living, human biological components rather than “animal models,” thus significantly improving the accuracy and speed of drug development.
Currently, the average drug takes about 10 years and $1 billion in research dollars to reach the market.
“The current testing system, involving mice and other animals, doesn’t reflect the human body,” Bentley said. “This leads to inaccurate results that require additional rounds of testing, dragging out the process for years.”
Bentley and colleagues from UMBI, the Maryland NanoCenter, the Institute for Systems Research (ISR) and the Clark School’s electrical and computer engineering and materials science and engineering departments, are collaborating to build devices that will allow a drug researcher to input both a drug to be tested and specific human biological components, such as proteins or cells. Such adevice makes multiple, simultaneous measurements of how those components respond to the drug, to determine whether the drug is successful. The device thus serves as a research environment that mimics the human body.
Improving Relationships and Diversifying the Site Selection Process
April 17th 2025In this episode of the Applied Clinical Trials Podcast, Liz Beatty, co-founder and chief strategy officer, Inato, discusses a number of topics around site engagement including community-based sites, the role of technology in improving site/sponsor relationships, how increased operational costs are impacting the industry, and more.
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.
FDA-Approved Gene Therapy Beqvez Shows Sustained Efficacy, Safety in Long-Term Hemophilia B Trial
April 17th 2025Beqvez (fidanacogene elaparvovec), an FDA-approved one-time gene therapy for hemophilia B, demonstrated sustained factor IX expression, low bleeding rates, and a favorable safety profile over long-term follow-up.