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Standalone DTx: clinical & economic evidence

11th November @ 10:45AM EDT

As DTx companies look for their place in the market, in order to convince the different healthcare stakeholders (payers, physicians, etc), they need to generate clinical and economic data that validates their products and services. The evidence requirements and challenges to generate it differ depending on the type of DTx; on this occasion we will focus on standalone DTx (DTx products used independently of drugs). Join this informal conversation with other senior leaders in the space to discuss the following: 


  • Level of clinical and economic evidence required for standalone DTx - how does this change depending on the stakeholder, mode of action, risk of the product, disease, etc? 
  • Particularities and Challenges of the Study Design for standalone DTx (e.g selecting the right comparators, inclusion/exclusion criteria, endpoints, the role of RWE, etc) 
  • What is the most efficient way to generate economic evidence? What methods can be used to generate this data in the different stages of a product?

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Standalone DTx: clinical & economic evidence

Todd Greenwood
Director, Evidence Generation and Outcomes Research, ZS
Matthias Essenpreis
Chief Technology Officer, Roche Diagnostics
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Standalone DTx: clinical & economic evidence

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11th November @ 10:45AM EDT

As DTx companies look for their place in the market, in order to convince the different healthcare stakeholders (payers, physicians, etc), they need to generate clinical and economic data that validates their products and services. The evidence requirements and challenges to generate it differ depending on the type of DTx; on this occasion we will focus on standalone DTx (DTx products used independently of drugs). Join this informal conversation with other senior leaders in the space to discuss the following: 


  • Level of clinical and economic evidence required for standalone DTx - how does this change depending on the stakeholder, mode of action, risk of the product, disease, etc? 
  • Particularities and Challenges of the Study Design for standalone DTx (e.g selecting the right comparators, inclusion/exclusion criteria, endpoints, the role of RWE, etc) 
  • What is the most efficient way to generate economic evidence? What methods can be used to generate this data in the different stages of a product?
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Participants

Participants

Todd Greenwood

Director, Evidence Generation and Outcomes Research, ZS

Matthias Essenpreis

Chief Technology Officer, Roche Diagnostics

Adam Samson

Sr. Director of Clinical Operations & Customer Success

Kyloon Chuah

Co-Founder & CEO @ Veriteos

Rick Bartels

Managing Partner , DTxCC

Chris Wasden

Chief Strategy Officer, Twill

Chris Cera

CEO, Arcweb Technologies

Number of Participants


Up to 12
Date  
November 11, 2021
Community

Standalone DTx: clinical & economic evidence

As DTx companies look for their place in the market, in order to convince the different healthcare stakeholders (payers, physicians, etc), they need to generate clinical and economic data that validates their products and services. The evidence requirements and challenges to generate it differ depending on the type of DTx; on this occasion we will focus on standalone DTx (DTx products used independently of drugs). Join this informal conversation with other senior leaders in the space to discuss the following: 


  • Level of clinical and economic evidence required for standalone DTx - how does this change depending on the stakeholder, mode of action, risk of the product, disease, etc? 
  • Particularities and Challenges of the Study Design for standalone DTx (e.g selecting the right comparators, inclusion/exclusion criteria, endpoints, the role of RWE, etc) 
  • What is the most efficient way to generate economic evidence? What methods can be used to generate this data in the different stages of a product?
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Standalone DTx: clinical & economic evidence

11th November @ 10:45AM EDT
Digital Therapeutics (DTx)

Standalone DTx: clinical & economic evidence

11th November @ 10:45AM EDT
Digital Therapeutics (DTx)
Todd Greenwood
Director, Evidence Generation and Outcomes Research, ZS
LinkedIn Profile
Matthias Essenpreis
Chief Technology Officer, Roche Diagnostics
LinkedIn Profile
Adam Samson
Sr. Director of Clinical Operations & Customer Success
LinkedIn Profile
Kyloon Chuah
Co-Founder & CEO @ Veriteos
LinkedIn Profile
Rick Bartels
Managing Partner , DTxCC
LinkedIn Profile
Chris Wasden
Chief Strategy Officer, Twill
LinkedIn Profile
Chris Cera
CEO, Arcweb Technologies
LinkedIn Profile

Standalone DTx: clinical & economic evidence

As DTx companies look for their place in the market, in order to convince the different healthcare stakeholders (payers, physicians, etc), they need to generate clinical and economic data that validates their products and services. The evidence requirements and challenges to generate it differ depending on the type of DTx; on this occasion we will focus on standalone DTx (DTx products used independently of drugs). Join this informal conversation with other senior leaders in the space to discuss the following: 


  • Level of clinical and economic evidence required for standalone DTx - how does this change depending on the stakeholder, mode of action, risk of the product, disease, etc? 
  • Particularities and Challenges of the Study Design for standalone DTx (e.g selecting the right comparators, inclusion/exclusion criteria, endpoints, the role of RWE, etc) 
  • What is the most efficient way to generate economic evidence? What methods can be used to generate this data in the different stages of a product?
When:
11th November @ 10:45AM EDT
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