The SCOPE of Things Podcast

Orr Inbar Discusses Saving Costs and Complications With Clinical Trial Simulations

Dec 10, 2024

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In this episode of the Scope of Things, host Deborah Borfitz covers concerns surrounding the study and treatment of obesity, a new “opening doors” initiative to clinical trials, debate over the European Union AI Act, the first international-level clinical study using secure multiparty computation, a hopeful treatment for kids with lethal brain tumors, and a ChatGPT tool created by the NIH to match potential volunteers to relevant studies. Joining the conversation is Orr Inbar, CEO and co-founder of QuantHealth, who discusses how his company is using AI to simulate clinical trials to alleviate costs and efficiency issues for the notoriously complicated drug development process. He also shares the proprietary tech powering QuantHealth’s AI and where he sees AI heading as 2025 unfolds.


SHOW NOTES

News Roundup
Perspectives on the EU AI Act

  • Insights about the rollout in Clinical Research News
  • Article in Clinical Research News about discussion at SCOPE Europe

Secure multiparty computation

Cell therapy for childhood brain cancer

TrialGPT tool

  • Study in Nature Communications

Guest
Orr Inbar, CEO and Co-Founder of Quant Health


GUEST BIO

Orr Inbar, CEO and Co-Founder, QuantHealth
Orr Inbar, CEO and Co-Founder of QuantHealth, an AI-powered clinical trial design company that works with three of the top ten pharmaceutical companies globally. Orr’s technical background spans data science, biomedical research, software engineering, and artificial intelligence, all with a focus on healthcare. Drawing upon this experience, Orr founded QuantHealth to address the disparities in clinical research that he felt could be overcome with novel quantitative methods to increase the success rate of 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.


Learn more

Clinical Research News Online