Behind the Breakthroughs

In this enlightening conversation, Mike Previte, CTO and co-founder of Element Biosciences, sheds light on his journey from Boston to groundbreaking advancements in biomedical technology. He discusses the limitations of current sequencing tools in capturing the dynamics of living cells and advocates for a 5D multiomics approach. Previte emphasizes the importance of integrating spatial and temporal dimensions in precision medicine. He also critiques traditional drug testing methods and highlights the potential of human-based models like organoids for safer and more effective therapies.

What do the steel industry and cutting-edge cancer treatments have in common? According to Hervé Affagard, CEO and co-founder of MaaT Pharma, more than you might think. In this episode, Hervé guides us through his journey from his early days as an engineer pioneering in industrial fields to spearheading the development of microbiome-based therapies for some of the world's most challenging diseases.Guided by a deeply personal mission inspired by his parents’ battles with cancer, Hervé shares how a revelation about the microbiome over a decade ago changed everything. From the first transformative trials on Clostridium difficile to MaaT Pharma’s work restoring microbial balance to treat graft-versus-host disease, Hervé explains how re-establishing the gut’s ecosystem can enhance immune function and offer new therapeutic possibilities for oncology and beyond.Stay up to date with the latest episodes of Behind the Breakthroughs by subscribing to the IPM eNewsletter here.Hosted by Jonathan D. GrinsteinProduced by Bill LevineAudio mixed and mastered by David MoselyMusic provided by penguinmusic Hosted on Acast. See acast.com/privacy for more information.

In May of 2020, drug developer Michelle Werner, PhD, learned that one of her three children—her middle child, Caffrey—was diagnosed with Duchenne muscular dystrophy (DMD). Werner went searching for an existing or experimental cure but came out empty-handed. So, after a couple of decades as a big pharma stalwart, Werner made a major career change and took over as CEO of Flagship Pioneering company Alltrna, which had a solution she believed could help children and families in similar positions—even if not Caffrey himself.In this Behind the Breakthroughs episode, Werner talks about the experience of being a mother to a child with a rare disease and her mission as Alltrna's CEO to find cures for all rare diseases, the majority of which have no approved therapies. Michelle goes in-depth into the mechanism behind Alltrna’s engineered transfer RNAs (tRNAs) and their broad applicability to all diseases caused by nonsense mutations leading to premature stop codons.Stay up to date with the latest episodes of Behind the Breakthroughs by subscribing to the IPM eNewsletter here.Produced by Bill LevineHosted by Jonathan D. GrinsteinAudio mixed and mastered by Jason MackMusic provided by Artem Hramushkin Hosted on Acast. See acast.com/privacy for more information.

Public health is greatly benefiting from population genomics screening, as it provides patients with risk education and treatment for symptoms of life-threatening diseases that they would not have been aware of through routine checkups. So, why hasn't population genomic screening realized its full potential? As an internist geneticist and Medical Affairs Director at Helix, this issue became all the more real for Cassie Hajek, MD, when she was diagnosed with breast cancer that evaded existing genetic testing procedures. In this earnest episode, Hajek shares how her experiences as both a cancer patient and a practitioner have helped her identify and build towards overcoming some of the barriers to maximizing population genomic screening for preventive medicine.Stay up to date with the latest episodes of Behind the Breakthroughs by subscribing to the IPM eNewsletter here.Produced by Bill LevineHosted by Jonathan D. GrinsteinAudio mixed and mastered by Jason MackMusic provided by Artem Hramushkin Hosted on Acast. See acast.com/privacy for more information.

Three biotech trailblazers—Patrick Hsu (co-founder of the Arc Institute), Serge Saxonov (co-founder and CEO of 10x Genomics), and Gilad Almogy (co-founder and CEO of Ultima Genomics)—join forces to discuss their groundbreaking collaboration on the virtual cell. This ambitious project leverages advanced AI and cutting-edge genomic technologies to model and predict cellular behavior, a leap forward in understanding complex biological systems. The trio dives deep into their shared vision, explaining how their partnership is redefining scientific research and pushing the boundaries of what’s possible in drug discovery and precision medicine.Stay up to date with the latest episodes of Behind the Breakthroughs by subscribing to the IPM eNewsletter here.Produced by Bill LevineHosted by Jonathan D. GrinsteinAudio mixed and mastered by Jason MackMusic provided by Artem Hramushkin Hosted on Acast. See acast.com/privacy for more information.

For years, Tempus operated in mystery—its website sparse on details while headlines announced massive funding and high-profile partnerships. The claim? AI-enabled solutions for personalized healthcare. Intrigued, I sought answers.In this episode, Kate Sasser, PhD, Chief Scientific Officer at Tempus, shared insights into how the company uses AI to analyze unstructured clinical data to develop patient-derived organoid models for therapeutic refinement. Most exciting is their vision of an interconnected “lab-in-a-loop” system—a cycle of real-world data, biological modeling, and AI analysis.Stay up to date with the latest episodes of Behind the Breakthroughs by subscribing to the IPM eNewsletter here.Produced by Bill LevineHosted by Jonathan D. GrinsteinAudio mixed and mastered by Jason MackMusic provided by Artem Hramushkin Hosted on Acast. See acast.com/privacy for more information.

Kian Sadeghi, the visionary founder of Nucleus Genomics, is shaking up personalized genomics with his direct-to-consumer whole genome sequencing service. He discusses the importance of patient agency and critiques traditional insurance biases against genetic testing. The conversation dives into the ambitious future of accessible genetic testing, inspired by personal tragedy. Sadeghi also reflects on the downfall of 23andMe and shares insights on how to avoid similar pitfalls while democratizing genomics for everyone.

Imagine a future where your ancestry not only tells a story about your past but also holds the key to your health. That's the vision drives Carlos D. Bustamante, PhD, population geneticist and founder of Galatea Bio, as he embarks on an ambitious mission: building a biobank of 10 million genomes to transform drug development and healthcare across Latin America. With thousands of founder populations scattered across the region—from the valleys of Medellín to the islands of the Caribbean—Latin America is a goldmine of genetic diversity. Yet, until now, it has been largely overlooked in genomic research. In this Behind the Breakthroughs episode, Bustamante explains why mapping this diversity can uncover genetic insights that will lead to better treatments for diseases that disproportionately affect these communities.Stay up to date with the latest episodes of Behind the Breakthroughs by subscribing to the IPM eNewsletter here.Produced by Bill LevineHosted by Jonathan D. GrinsteinMusic provided by Artem HramushkinAudio mixed and mastered by Jason Mack Hosted on Acast. See acast.com/privacy for more information.

Josh Denny, MD, is a trailblazer in precision medicine whose journey was deeply influenced by his family’s struggles with cystic fibrosis, a disease that claimed the lives of four of his grandparents’ children. This personal connection fueled his pursuit of a career blending medicine, genetics, and technology, leading to groundbreaking work in medical informatics and personalized healthcare.In this episode of Behind the Breakthroughs, we delve into Josh’s leadership of the All of Us Research Program. Since its launch in 2018, this ambitious initiative has enrolled 850,000 participants and collected over 400,000 genomic profiles. Its goal: to harness diverse biological data to advance understanding of health disparities, rare diseases, and common conditions. Discover how Josh’s work is revolutionizing healthcare, from life-saving genetic testing to targeted therapies, and shaping a future where medicine is tailored to every individual’s unique genetic and environmental profile.Stay up to date with the latest episodes of Behind the Breakthroughs by subscribing to the IPM eNewsletter here.Produced by Bill LevineHosted by Jonathan D. GrinsteinMusic provided by Artem HramushkinAudio mixed and mastered by Jason Mack Hosted on Acast. See acast.com/privacy for more information.

The sage-like Uli Stilz, PhD, Vice President of Novo Nordisk, provides insight into the inner workings of Novo Nordisk’s Bio Innovation Hub, which he founded in Boston, to tackle complex, multifactorial diseases that impact billions of people, such as diabetes and cardiometabolic diseases.Stay up to date with the latest episodes of Behind the Breakthroughs by subscribing to the IPM eNewsletter here.Produced by Bill LevineHosted by Jonathan D. GrinsteinMusic provided by Artem HramushkinAudio mixed and mastered by Jason Mack Hosted on Acast. See acast.com/privacy for more information.