CRISPR - From Trial to Pharmacy Shelf: Scaling the First Gene-Editing Cure episode artwork

EPISODE · Apr 10, 2026 · 26 MIN

CRISPR - From Trial to Pharmacy Shelf: Scaling the First Gene-Editing Cure

from CRISPR · host Inception Point AI

Ryan Cole examines Casgevy, the world's first approved CRISPR medicine for sickle cell disease and beta thalassemia. While revolutionary, delivering this autologous gene therapy faces massive challenges: a $2.2 million price tag, months-long manufacturing, only 50 global treatment centers, and access barriers in regions with highest disease burden. Loved this episode? Discover more original shows from the Quiet Please Network at QuietPlease.ai, explore our curated favorites here amzn.to/42YoQGI, and catch just a slice of our AI hosts in action on Instagram at instagram.com/claredelish and YouTube at youtube.com/@DIYHOMEGARDENTV This content was created in partnership and with the help of Artificial Intelligence AI.

Ryan Cole examines Casgevy, the world's first approved CRISPR medicine for sickle cell disease and beta thalassemia. While revolutionary, delivering this autologous gene therapy faces massive challenges: a $2.2 million price tag, months-long manufacturing, only 50 global treatment centers, and access barriers in regions with highest disease burden. Loved this episode? Discover more original shows from the Quiet Please Network at QuietPlease.ai, explore our curated favorites here amzn.to/42YoQGI, and catch just a slice of our AI hosts in action on Instagram at instagram.com/claredelish and YouTube at youtube.com/@DIYHOMEGARDENTV This content was created in partnership and with the help of Artificial Intelligence AI.

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CRISPR - From Trial to Pharmacy Shelf: Scaling the First Gene-Editing Cure

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Finding Genius Podcast Richard Jacobs Podcast interviews with genius-level (top .1%) practitioners, scientists, researchers, clinicians and professionals in Cancer, 3D Bio Printing, CRISPR-CAS9, Ketogenic Diets, the Microbiome, Extracellular Vesicles, and more.Subscribe today for the latest medical, health and bioscience insights from geniuses in their field(s). DNA Today: A Genetics Podcast Kira Dineen, Gene Pool Media Discover New Advances in the world of genetics, from technology like CRISPR to rare diseases to new research. For over a decade, multi-award winning podcast ”DNA Today” has brought you the voices of leaders in genetics. Host Kira Dineen brings her genetics expertise to interview geneticists, genetic counselors, patient advocates, biotech leaders, researchers, and more.***Best 2020, 2021, and 2022 Science and Medicine Podcast Award Winner***Learn more (and stream all 380+ episodes) at DNAtoday.com. You can contact the show at [email protected] show is part of "Gene Pool Media: The Science Podcast Network" head to GenePoolMedia.com to explore all our science themed shows.  Designer Genes: A Conversation about CRISPR Efrain C., Hope J., Maria R., Sanjay A.L. From Mendel to modern laboratories, genome-editing has fascinated the minds of many. Recently, the CRISPR-Cas9 system has been a major advancement in genome editing. Though this newly discovered mechanism has shown the potential to cure life-threatening genetic problems, the novelty of it has caused some concerns over potential ethical violations. Designer Genes is a conversation hosted by four curious biology undergraduates at Emory University that attempts to bridge the gap between scientific knowledge of CRISPR and the general public’s understanding. See website for references. Flot.bio x Philip Hemme Flot.bio Watch the #1 Biotech Podcast in Europe to grow. Hosted by Philip Hemme. 25k monthly views. Free.Guests include Antoine Papiernik @Sofinnova, Werner Lanthaler @Evotec, Ingmar Hoerr @CureVac, Bernat Olle @Vedanta, Johannes Fruehauf @BioLabs, Rodger Novak @CRISPR Tx, Agnete Fredriksen @Nykode, Mike Ward, Thomas Clozel @Owkin, Marc de Garidel @Abivax, Sander van Deventer @VectorY & Forbion, Jens Nielsen @BII, Edwin Moses, Bahija Jallal @Immunocore, and more. Your host Philip animates the conversation to dig out exciting, and sometimes contrarian, ideas.

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This episode is 26 minutes long.

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This episode was published on April 10, 2026.

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Ryan Cole examines Casgevy, the world's first approved CRISPR medicine for sickle cell disease and beta thalassemia. While revolutionary, delivering this autologous gene therapy faces massive challenges: a $2.2 million price tag, months-long...

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