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Content provided by Alexander Schacht and Benjamin Piske, biometricians, statisticians and leaders in the pharma industry, Alexander Schacht, Benjamin Piske, and Leaders in the pharma industry. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Alexander Schacht and Benjamin Piske, biometricians, statisticians and leaders in the pharma industry, Alexander Schacht, Benjamin Piske, and Leaders in the pharma industry 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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Top 8: The Single Arm Studies and What are the Alternatives?

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Manage episode 506628118 series 2400265
Content provided by Alexander Schacht and Benjamin Piske, biometricians, statisticians and leaders in the pharma industry, Alexander Schacht, Benjamin Piske, and Leaders in the pharma industry. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Alexander Schacht and Benjamin Piske, biometricians, statisticians and leaders in the pharma industry, Alexander Schacht, Benjamin Piske, and Leaders in the pharma industry 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.
Interview with Anja Schiel

Why You Should Listen:

f you’ve ever wondered whether single-arm studies are “good enough” for regulators or HTA bodies, this episode will challenge your assumptions. Anja Schiel, one of Europe’s leading voices at the regulator–HTA interface, explains why comparisons matter, where single-arm designs break down, and what smarter alternatives exist.

You’ll walk away with:

✔ A clearer understanding of the limits of single-arm trials

✔ Practical strategies for choosing comparators that strengthen your evidence package

✔ Insight into adaptive and hybrid designs that balance efficiency with rigor

✔ A regulator/HTA insider’s perspective on what decision-makers really need from statisticians

Episode Highlights:

00:01:36 – Meet Anja Schiel and learn how she bridges regulation and HTA

00:02:28 – Why connecting regulators and HTA bodies early matters for drug development

00:06:07 – Where single-arm studies often fall short in real-world decision-making

00:08:01 – What accelerated approvals have taught us about assumptions in trial design

00:10:17 – Why comparison—not just randomization—is at the heart of sound evidence

00:12:12 – The pitfalls of relying on literature-based or naïve comparisons

00:16:54 – How regulators and HTA approach evidence differently

00:17:00 – What “concurrent control” really means and why it’s crucial

00:20:33 – Strategic thinking when selecting comparators for long-term value

00:26:00 – The role of adaptive and hybrid designs in modern trials

00:33:59 – Ethical considerations when trial designs fall short

00:36:26 – Why rare diseases demand smarter collaboration and evidence planning

00:40:25 – Communicating study objectives and estimands clearly for all stakeholders

00:44:55 – Final takeaways: how statisticians can lead the push for better designs

Links:

🔗 The Effective Statistician Academy – I offer free and premium resources to help you become a more effective statistician.

🔗 Medical Data Leaders Community – Join my network of statisticians and data leaders to enhance your influencing skills.

🔗 My New Book: How to Be an Effective Statistician - Volume 1 – It’s packed with insights to help statisticians, data scientists, and quantitative professionals excel as leaders, collaborators, and change-makers in healthcare and medicine.

🔗 PSI (Statistical Community in Healthcare) – Access webinars, training, and networking opportunities.

Join the Conversation:
Did you find this episode helpful? Share it with your colleagues and let me know your thoughts! Connect with me on LinkedIn and be part of the discussion.

Subscribe & Stay Updated:
Never miss an episode! Subscribe to The Effective Statistician on your favorite podcast platform and continue growing your influence as a statistician.

  continue reading

461 episodes

Artwork
iconShare
 
Manage episode 506628118 series 2400265
Content provided by Alexander Schacht and Benjamin Piske, biometricians, statisticians and leaders in the pharma industry, Alexander Schacht, Benjamin Piske, and Leaders in the pharma industry. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Alexander Schacht and Benjamin Piske, biometricians, statisticians and leaders in the pharma industry, Alexander Schacht, Benjamin Piske, and Leaders in the pharma industry 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.
Interview with Anja Schiel

Why You Should Listen:

f you’ve ever wondered whether single-arm studies are “good enough” for regulators or HTA bodies, this episode will challenge your assumptions. Anja Schiel, one of Europe’s leading voices at the regulator–HTA interface, explains why comparisons matter, where single-arm designs break down, and what smarter alternatives exist.

You’ll walk away with:

✔ A clearer understanding of the limits of single-arm trials

✔ Practical strategies for choosing comparators that strengthen your evidence package

✔ Insight into adaptive and hybrid designs that balance efficiency with rigor

✔ A regulator/HTA insider’s perspective on what decision-makers really need from statisticians

Episode Highlights:

00:01:36 – Meet Anja Schiel and learn how she bridges regulation and HTA

00:02:28 – Why connecting regulators and HTA bodies early matters for drug development

00:06:07 – Where single-arm studies often fall short in real-world decision-making

00:08:01 – What accelerated approvals have taught us about assumptions in trial design

00:10:17 – Why comparison—not just randomization—is at the heart of sound evidence

00:12:12 – The pitfalls of relying on literature-based or naïve comparisons

00:16:54 – How regulators and HTA approach evidence differently

00:17:00 – What “concurrent control” really means and why it’s crucial

00:20:33 – Strategic thinking when selecting comparators for long-term value

00:26:00 – The role of adaptive and hybrid designs in modern trials

00:33:59 – Ethical considerations when trial designs fall short

00:36:26 – Why rare diseases demand smarter collaboration and evidence planning

00:40:25 – Communicating study objectives and estimands clearly for all stakeholders

00:44:55 – Final takeaways: how statisticians can lead the push for better designs

Links:

🔗 The Effective Statistician Academy – I offer free and premium resources to help you become a more effective statistician.

🔗 Medical Data Leaders Community – Join my network of statisticians and data leaders to enhance your influencing skills.

🔗 My New Book: How to Be an Effective Statistician - Volume 1 – It’s packed with insights to help statisticians, data scientists, and quantitative professionals excel as leaders, collaborators, and change-makers in healthcare and medicine.

🔗 PSI (Statistical Community in Healthcare) – Access webinars, training, and networking opportunities.

Join the Conversation:
Did you find this episode helpful? Share it with your colleagues and let me know your thoughts! Connect with me on LinkedIn and be part of the discussion.

Subscribe & Stay Updated:
Never miss an episode! Subscribe to The Effective Statistician on your favorite podcast platform and continue growing your influence as a statistician.

  continue reading

461 episodes

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