The SCOPE of Things Podcast

The Missing Link in Clinical Trials and Brain Monitoring: Consistent EEG Use

April 2, 2024

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In this month’s episode of the Scope of Things, host Deborah Borfitz covers the latest news and emerging trends, including the launch of a company using single-solution software to connect a global network of clinical trial sites to study sponsors, a pharmacy-first program in the UK, a centralized staffing initiative at the National Cancer Institute, progress in getting patient-derived organoids into clinical trials to evaluate drug response, and more. She also speaks with Lifelines Neuro’s chief scientific officer Dona Murphey, M.D., Ph.D. about shortcomings in the way EEGs are being use in clinical trials to monitor participants with potential brain damage, how EEG monitoring should be used in clinical research, and what the FDA has to say about all of this.


Show Notes

News Roundup

Launch of Pi Health

Pharmacy First initiative in the UK

Pediatric rare disease research

  • Article in Hepatology about utility of real-world cohort

NCI Virtual Clinical Trials Office

Precision oncology clinical trial landscape

Translational Research Innovation Program

Patient-derived organoids in clinical trials

  • Study in Cells Tissues Organs

Guest


Dona Murphey, M.D., Ph.D., chief scientific officer for Lifelines Neuro
Dona is a neurologist, neuroscientist, historian of science, and community health worker educated at Harvard and Baylor College of Medicine. She currently serves as principal consultant at In Phase Neuro and fractional chief scientific officer at Synthesys Brain Health (a joint endeavor between Lifelines Neuro and Neurovative Diagnostics), specializing in the area of EEG in clinical trials.

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Meet the Host

Deborah Borfitz

Deborah Borfitz

Deborah Borfitz serves as host of The Scope of Things podcast. She is also senior science writer for Cambridge Healthtech Institute and is the lead contributor to Clinical Research News, Bio-IT World, and Diagnostics World News. Deborah has a long and varied career in journalism, much of it as an independent writer with a heavy focus on healthcare and clinical research. She was introduced to the world of clinical trials 25 years ago by advisory board member Ken Getz and in 2001 co-authored a book with him on the informed consent process.


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