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?