Weekly reads: cell and gene therapy deregulation, axed grant database, H3.3 in mESCs, remembering James Till

It’s been a crazy week on the cell and gene therapy front. We live in strange times more generally.

I just wrote about a Thursday FDA cell and gene therapy roundtable that generally promoted the idea of less oversight. And far more speed to human use.

RFK Jr. was present at the end and spoke.

Almost all the speakers, often top academic researchers, pushed for the FDA to exercise much less oversight here.

RFK Jr., cell and gene therapy
RFK Jr. with Russell Brand and Dr. Oz. Instagram photo. Kennedy and Oz spoke at a cell and gene therapy meeting at the FDA this past Thursday.

A growing feeling of unease about coming cell and gene therapy deregulation

For example, pioneer Carl June floated the idea that investigational autologous gene therapies should only initially being regulated locally by IRBs and not the FDA. It’d be super risky.

I came away from the meeting initially feeling it was a mostly positive gathering. Although the risks of the speedy or minimal FDA oversight emphasized at the meeting worried me, I tried to focus on the upside of the unique gathering. However, as time has passed, a feeling of deeper concern about the meeting has taken over.

Part of that shift may have been influenced by the revelation that Kennedy received unproven stem cells himself. In the podcast where he revealed his stem cell treatment, he also suggested much wider access to such cells or other similar unproven therapies for Americans would be a good thing.

Big changes are on the horizon for the FDA related to our fields. A risky experiment in deregulation is likely coming.

Recommended reads

Blast from the past: my interview with Steven Pinker

Steven Pinker interview: case against bioethocrats & CRISPR germline ban.

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1 thought on “Weekly reads: cell and gene therapy deregulation, axed grant database, H3.3 in mESCs, remembering James Till”

  1. Thank you for sharing the paper on fgf receptor and tumor treating fields. What a fascinating approach to oncology.

    Do we know the mechanism of how this approach works?

    If I remember correctly they were trying to generate an electromagnetic signature similar to siRNA for an immune checkpoint?

    Any thoughts would be greatly appreciated

    Tom

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