Sign up to save your podcasts
Or
Share Navigating the FDA Landscape: More Changes, and What's Next?
Share to email
Share to Facebook
Share to X
Share to email
Share to Facebook
Share to X
Or
Navigating the FDA Landscape: More Changes, and What's Next?
In this episode, Eric Hardter and guest Kelsey Lenoch discuss recent US FDA developments, including leadership changes at CBER and CDER, staffing impacts on orphan product reviews, and the new Rare Disease Evidence Principles aimed at accelerating approvals for rare and ultra-rare conditions.
They also explore evolving trial endpoints in oncology (including surrogate measures and ctDNA), transparency moves such as the public release of Complete Response Letters and the industry’s reactions, updates on the National Priority Voucher Program, and the FDA Pre-Check initiative to boost domestic drug manufacturing.
Tune in for an in-depth discussion offering timely updates and expert perspectives on what may be ahead for drug development stakeholders.
🎧 Chapters
Welcome and Introductions (00:00:05)
Recap and Recent US Regulatory Affairs Developments (00:01:00)
Dr. Vinay Prasad’s Removal and Return to FDA CBER (00:01:20)
New Appointments at FDA CDER (00:02:17)
FDA Staffing Shortages and Impact on Orphan Products (00:04:22)
Rare Disease Evidence Principles Announcement (00:05:29)
FDA’s Rare Disease Innovation Hub and Ultra-Rare Disease Focus (00:07:19)
Novel Endpoints in Oncology Drug Development (00:09:31)
FDA/AACR Joint Meeting on Novel Endpoints (00:10:12)
Challenges with Overall Survival as an Endpoint (00:10:36)
FDA’s Evolving Guidance on Endpoints (00:11:04)
Post-Licensure Requirements and Surrogate Endpoints (00:11:48)
Case Study: Myelofibrosis Drug and Patient-Reported Endpoints (00:12:49)
Standardization Challenges for New Endpoints (00:13:55)
Circulating Tumor DNA as a Biomarker (00:14:51)
FDA’s Release of Complete Response Letters – Phase Two (00:16:06)
Pros and Cons of Public Complete Response Letters (00:17:19)
Industry Pushback and Sponsor Transparency (00:19:22)
Case Study: Lycos Therapeutics and Psychedelic Drug Approval (00:21:09)
Accessing and Mining Complete Response Letter Data (00:22:34)
National Priority Voucher Program Update (00:23:43)
FDA Pre-Check Program for Domestic Manufacturing (00:24:26)
Closing Remarks and Future Outlook (00:25:12)
View all episodes
By Boyds
5
55 ratings
In this episode, Eric Hardter and guest Kelsey Lenoch discuss recent US FDA developments, including leadership changes at CBER and CDER, staffing impacts on orphan product reviews, and the new Rare Disease Evidence Principles aimed at accelerating approvals for rare and ultra-rare conditions.
They also explore evolving trial endpoints in oncology (including surrogate measures and ctDNA), transparency moves such as the public release of Complete Response Letters and the industry’s reactions, updates on the National Priority Voucher Program, and the FDA Pre-Check initiative to boost domestic drug manufacturing.
Tune in for an in-depth discussion offering timely updates and expert perspectives on what may be ahead for drug development stakeholders.
🎧 Chapters
Welcome and Introductions (00:00:05)
Recap and Recent US Regulatory Affairs Developments (00:01:00)
Dr. Vinay Prasad’s Removal and Return to FDA CBER (00:01:20)
New Appointments at FDA CDER (00:02:17)
FDA Staffing Shortages and Impact on Orphan Products (00:04:22)
Rare Disease Evidence Principles Announcement (00:05:29)
FDA’s Rare Disease Innovation Hub and Ultra-Rare Disease Focus (00:07:19)
Novel Endpoints in Oncology Drug Development (00:09:31)
FDA/AACR Joint Meeting on Novel Endpoints (00:10:12)
Challenges with Overall Survival as an Endpoint (00:10:36)
FDA’s Evolving Guidance on Endpoints (00:11:04)
Post-Licensure Requirements and Surrogate Endpoints (00:11:48)
Case Study: Myelofibrosis Drug and Patient-Reported Endpoints (00:12:49)
Standardization Challenges for New Endpoints (00:13:55)
Circulating Tumor DNA as a Biomarker (00:14:51)
FDA’s Release of Complete Response Letters – Phase Two (00:16:06)
Pros and Cons of Public Complete Response Letters (00:17:19)
Industry Pushback and Sponsor Transparency (00:19:22)
Case Study: Lycos Therapeutics and Psychedelic Drug Approval (00:21:09)
Accessing and Mining Complete Response Letter Data (00:22:34)
National Priority Voucher Program Update (00:23:43)
FDA Pre-Check Program for Domestic Manufacturing (00:24:26)
Closing Remarks and Future Outlook (00:25:12)
More shows like Conversations in Drug Development
View all
Radiolab
43,919 Listeners
Freakonomics Radio
32,068 Listeners
Pivot
9,576 Listeners
The Daily
112,840 Listeners
Up First from NPR
56,555 Listeners
The Readout Loud
324 Listeners
The Journal.
6,053 Listeners
Think Fast Talk Smart: Communication Techniques
805 Listeners
The Prof G Pod with Scott Galloway
5,533 Listeners
Business Of Biotech
86 Listeners
BioCentury This Week
33 Listeners
Biotech Hangout
19 Listeners
The Rest Is Politics
3,141 Listeners
HBR On Leadership
167 Listeners
The Top Line
13 Listeners