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Christopher D: Personalized CRISPR Therapy and the Future of Rare Disease Care
Sep 27, 2026, 07:57

Christopher D: Personalized CRISPR Therapy and the Future of Rare Disease Care

Christopher D., Executive Specialty Sales at AbbVie, shared a post on LinkedIn:

“A baby named KJ Muldoon is why I can’t stop thinking about where medicine is headed.

KJ was born with a rare genetic disorder that stopped his liver from clearing ammonia from his blood.

The old options: a transplant, or irreversible damage. Instead, his team built a personalized CRISPR therapy for his exact mutation and delivered it straight to his liver.

It worked he’s the world’s first patient treated this way.

That case is part of a bigger shift in liver and rare disease care right now:

Base or prime editing moving from lab to bedside for hemophilia, metabolic disorders

AI catching fatty liver disease earlier and personalizing treatment

Liver organoids letting researchers test therapies before they reach a patient

The liver’s biology making it a prime target for next gen gene therapy

‘Rare disease’ used to mean ‘no good options.’ That’s changing fast.

What’s the most exciting thing you’ve seen in this space lately?

Sources:

NIH, NCATS, Baby KJ story:

Jackson Laboratory, gene editing for rare liver disorder”

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