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FDA Regulation On Gene Therapy | The Brainstorm EP 96
In this episode of the Brainstorm, Sam, Nick, and Multiomics Research Analyst, Shea Wihlborg, dive into the complexities of the FDA's recent decisions and their implications for gene therapy. They discuss the controversial halt of a Duchenne muscular dystrophy treatment, the role of AI in drug discovery, and the exciting future of genomics.
If you know ARK, then you probably know about our long-term research projections, like estimating where we will be 5-10 years from now! But just because we are long-term investors, doesn’t mean we don’t have strong views and opinions on breaking news. In fact, we discuss and debate this every day. So now we’re sharing some of these internal discussions with you in our new video series, “The Brainstorm”, a co-production from ARK and Public.com. Tune in every week as we react to the latest in innovation. Here and there we’ll be joined by special guests, but ultimately this is our chance to join the conversation and share ARK’s quick takes on what’s going on in tech today.
Key Points From This Episode:
- Discussion on the FDA's recent halt of a Duchenne muscular dystrophy treatment due to safety concerns.
- Exploration of the role of AI in improving drug discovery and clinical trials.
- Insights into the future of gene therapies for both rare and common diseases.
- The potential impact of regulatory changes on innovation in the biotech industry.
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Published on 1 month ago