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Creating virtuous cycles in drug development with Rob Freishtat

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Manage episode 478559362 series 3526489
Content provided by Sam Parnell & Ivanna Rosendal, Sam Parnell, and Ivanna Rosendal. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Sam Parnell & Ivanna Rosendal, Sam Parnell, and Ivanna Rosendal or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://podcastplayer.com/legal.

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Rob Freistat, President of Uncommon Cures, discusses how clinical trials are transforming to accelerate drug development and ensure patients receive treatments faster, particularly in the rare disease space.
• Current market uncertainty and investment challenges in biotech, especially for rare disease research
• Approximately two-thirds of clinical trial processes add no value and aren't required by regulations
• Many clinical trial failures occur not because drugs don't work but because trials can't recruit enough patients
• Companies often treat development phases as "islands" rather than planning for commercial success from the beginning
• Rare disease economics require greater efficiency since development costs must be recovered from much smaller patient populations
• Reviving shelved drug candidates represents a potentially valuable opportunity
• Patients should have greater input in trial design and outcome measures that matter to them
• Better communication between sponsors and regulators could significantly improve drug development
________
Reach out to Ivanna Rosendal
Join the conversation on our LinkedIn page

  continue reading

Chapters

1. Creating virtuous cycles in drug development with Rob Freishtat (00:00:00)

2. Introduction to Transformation in Trials (00:00:19)

3. Current Market Dynamics in Biotech (00:01:45)

4. Streamlining Drug Development Processes (00:08:22)

5. Planning for Success in Drug Development (00:13:39)

6. The Economics of Rare Disease Drugs (00:22:31)

7. Improving Communication with Regulators (00:37:51)

76 episodes

Artwork
iconShare
 
Manage episode 478559362 series 3526489
Content provided by Sam Parnell & Ivanna Rosendal, Sam Parnell, and Ivanna Rosendal. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Sam Parnell & Ivanna Rosendal, Sam Parnell, and Ivanna Rosendal or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://podcastplayer.com/legal.

Send us a text

Rob Freistat, President of Uncommon Cures, discusses how clinical trials are transforming to accelerate drug development and ensure patients receive treatments faster, particularly in the rare disease space.
• Current market uncertainty and investment challenges in biotech, especially for rare disease research
• Approximately two-thirds of clinical trial processes add no value and aren't required by regulations
• Many clinical trial failures occur not because drugs don't work but because trials can't recruit enough patients
• Companies often treat development phases as "islands" rather than planning for commercial success from the beginning
• Rare disease economics require greater efficiency since development costs must be recovered from much smaller patient populations
• Reviving shelved drug candidates represents a potentially valuable opportunity
• Patients should have greater input in trial design and outcome measures that matter to them
• Better communication between sponsors and regulators could significantly improve drug development
________
Reach out to Ivanna Rosendal
Join the conversation on our LinkedIn page

  continue reading

Chapters

1. Creating virtuous cycles in drug development with Rob Freishtat (00:00:00)

2. Introduction to Transformation in Trials (00:00:19)

3. Current Market Dynamics in Biotech (00:01:45)

4. Streamlining Drug Development Processes (00:08:22)

5. Planning for Success in Drug Development (00:13:39)

6. The Economics of Rare Disease Drugs (00:22:31)

7. Improving Communication with Regulators (00:37:51)

76 episodes

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