CGTLive®’s Weekly Rewind – August 9, 2024

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Review top news and interview highlights from the week ending August 9, 2024.

CGTLive®’s Weekly Rewind

CGTLive®’s Weekly Rewind

Welcome to CGTLive®’s Weekly Rewind! We’ve compiled 5 highlights from this week’s coverage of advances in gene and cell therapies, including FDA actions, notable research, and interviews with experts across the field.

1. Indapta to Evaluate g-NK Therapy in Trial for Progressive Multiple Sclerosis

The trial evaluating the safety and tolerability of IDP-023 will be led by Stanford and UCSF.

2. Joshua M. Hare, MD, on Working to Address Unmet Needs in Alzheimer Disease With Lomecel-B Cell Therapy

The cofounder and chief science officer of Longeveron discussed working to show potential benefits in a follow-up phase 3 trial.

3. FDA Modifies CAR-T Risk Strategies to Lower Healthcare Burden

A recent study also recommended a shorter, more flexible monitoring period post-CAR–T therapy.

4. David Dimmock, MBBS, on a Promising Case Study of Ultra-Rare, AI-Guided, ASO Development

The chief medical officer at Creyon Bio discussed findings from a treated patient with a TNP02 missense mutation.

5. Pivotal Bria-IMT Trial Hopes to Support BLA for Advanced Metastatic Breast Cancer

BriaCell initiated the pivotal phase 3 BRIA-ABC trial in October 2023.

Recent Videos
Chun-Yu Chen, PhD, a research scientist at Seattle Children’s Research Institute
William Chou, MD, on Targeting Progranulin With Gene Therapy for Frontotemporal Dementia
Alexandra Collin de l’Hortet, PhD, the head of therapeutics at Epic Bio
David Dimmock, MBBS, on Accelerating Therapy Discovery and Approval With AI David Dimmock, MBBS, on Accelerating Therapy Discovery and Approval With AI
Joshua M. Hare, MD, on Working to Address Unmet Needs in Alzheimer Disease With Lomecel-B Cell Therapy
David Dimmock, MBBS, on a Promising Case Study of Ultra-Rare, AI-Guided, ASO Development
William Chou, MD, on Expanding Frontotemporal Dementia Gene Therapy to Both GRN and C9orf72 Mutations
Michael Severino on In Vivo Gene Editing With RNA Gene Writers
Chris Wright, MD, PhD, on Annelloviruses, a Potential Alternative to AAV for Gene Therapy
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