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One Month After Glafabra's FDA INTERACT Meeting

Glafabra
Posted at Aug 14

One month since Glafabra's FDA INTERACT meeting.

That July 16 conversation shapes the IND protocol we're building now: endpoint strategy, patient selection criteria, conditioning approach. None of that gets finalized overnight — it's weeks of translating regulatory feedback into a protocol document.

For those tracking the timeline: IND filing stays targeted for mid-2027. First patient enrolled tar...more

Categories: Advanced Therapeutics  |  Cell & Gene Therapy  |  Clinical Research  |  Drug Development  |  Fabry Disease  |  Rare Disease
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Can Fabry Disease Occur With No Family History? — DECODE No. 12

Glafabra
Posted at Aug 13

Answer to the question last time on August 10: a father passes his only X chromosome to every daughter and his Y to every son — so every daughter inherits his Fabry variant, and no son does.)

Most Fabry cases run in families. But every so often, someone is diagnosed with zero family history at all — no parent, no sibling, nothing in the records.

What causes Fabry disease to show up with no family ...more

Categories: Advanced Therapeutics  |  Cell & Gene Therapy  |  Clinical Research  |  Drug Development  |  Fabry Disease  |  Rare Disease
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Why Does Live-cel Use Hematopoietic Stem Cells?

Glafabra
Posted at Aug 12

Why build a gene therapy around a blood stem cell instead of a virus alone?

A hematopoietic stem cell (HSC) — the cell that gives rise to your entire blood and immune system — can be corrected once, outside the body, and then put back in. It engrafts permanently, and its corrected descendants keep making the missing enzyme for years.

That's the foundation Live-cel is built on: harvest, correct, re...more

Categories: Advanced Therapeutics  |  Cell & Gene Therapy  |  Clinical Research  |  Drug Development  |  Fabry Disease  |  Rare Disease
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Meet Glafabra's CEO & Co-Founder, Chris Hopkins

Glafabra
Posted at Aug 11

Meet the person leading this: Chris Hopkins, CEO & Co-Founder.

Chris is a geneticist, biochemist, and entrepreneur who's spent his career at the intersection of science and company-building. He guided the acquisition of Knudra Transgenics by InVivo Biosystems, raised over $5M in venture capital and $7M in non-dilutive SBIR funding, licensed CRISPR technology in 2014 — shortly after it was inve...more

Categories: Advanced Therapeutics  |  Cell & Gene Therapy  |  Clinical Research  |  Drug Development  |  Fabry Disease  |  Rare Disease
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Why Do All Daughters of an Affected Father Inherit Fabry Disease? — DECODE No. 11

Glafabra
Posted at Aug 10

(Answer to the question last time on August 6: Fabry disease is X-linked — the GLA gene sits on the X chromosome, so the pattern plays out differently for men and women.)

Here's the quirk that surprises people. A father with Fabry disease passes the condition to every single one of his daughters — but to none of his sons.

Why does it break down exactly that way? Drop your guess in the comments bel...more

Categories: Advanced Therapeutics  |  Cell & Gene Therapy  |  Clinical Research  |  Drug Development  |  Fabry Disease  |  Rare Disease
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What's New in Glafabra's Testing the Waters Campaign

Glafabra
Posted at Aug 7

One month into Testing the Waters. Here's what's changing for month two.

More real faces. Starting this Tuesday, we're introducing you to the people building Glafabra — one team member at a time, starting with our CEO.

DECODE keeps going, but simpler: no more separate answer-comment days later. Each new riddle now opens with last time's answer, right in the post.

And more of Glafabra's actual stor...more

Categories: Advanced Therapeutics  |  Cell & Gene Therapy  |  Clinical Research  |  Drug Development  |  Fabry Disease  |  Rare Disease
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