Gene therapy is in crisis. Its top minds searched for a solution
W ASHINGTON — Jennifer Puck has successfully treated 10 children with a gene therapy for a fatal disorder that decimates their immune system. But she has no idea how to get her drug approved and frankly is running out of ideas. “I wish I had a clue about where to go from here,” said Puck, an immunologist at University of California, San Francisco, from a plush chair above Union Station. advertisement The problem is simple: Size. Puck’s therapy is for a disease, Artemis-SCID, that affects just two to three new U.S. patients every year — far too few for a company to generate a profit, or to even run the kind of studies regulators usually demand before approving drugs. She is far from alone. Puck’s case is emblematic of a crisis that drew a few dozen gene therapy researchers and a couple of key advocates and federal officials to an invite-only workshop in Washington last month, a quagmire born of the field’s own success. After a half-century of fits-and-starts, the tools of molecular biol
W ASHINGTON — Jennifer Puck has successfully treated 10 children with a gene therapy for a fatal disorder that decimates their immune system. But she has no idea how to get her drug approved and frankly is running out of ideas. “I wish I had a clue about where to go from here,” said Puck, an immunologist at University of California, San Francisco, from a plush chair above Union Station. Advertisement The problem is simple: Size. Puck’s therapy is for a disease, Artemis-SCID , that affects just two to three new U.S. patients every year — far too few for a company to generate a profit, or to eve
Explore this link on the map →related reading
- Medical breakthroughs in 2025 - by Saloni Dattaniscientificdiscovery.dev
- Pearl Freier on X: "Cell & gene therapies were 2.5x more likely to receive FDA approval after entering Phase 1 than other drug types according to research by the NEWDIGs initiative at Tufts Medical Center h/t @DrPHanley & @alliancerm . @NatRevDrugDisc paper below 1/n https://t.co/DN4k7qWrAt" / Xx.com
- The pharma industry from Paul Janssen to today: why drugs got harder to develop and what we can do about it | Alex’s blogatelfo.github.io
- Going Founder Mode On Cancer - by Elliot Hershbergcenturyofbio.com
- Medicine's Endgamenotboring.co
- Mnemonic portraits for 19,023 human genes — LessWronglesswrong.com
- How many hemophilia patients actually want gene therapy?statnews.com
- Curative gene therapies for rare diseases - PMCncbi.nlm.nih.gov
- Where are all the trillion dollar biotechs?ladanuzhna.xyz
- Frontiers | Current and Future Prospects for Gene Therapy for Rare Genetic Diseases Affecting the Brain and Spinal Cordfrontiersin.org
- Significantly Enhancing Adult Intelligence With Gene Editing May Be Possible — LessWronglesswrong.com
- The Frontier in 2025renaissancephilanthropy.org