Regulators, Health Technology Assessment (HTA) agencies and health care payers are increasingly demanding Real World Evidence (RWE) to support both iStock_000060670584_Medium-1 copyinitial product approval/reimbursement as well as continuing approval/reimbursement over a product’s life cycle.

Clinical trials are frequently conducted to demonstrate safety and efficacy, Non-Interventional Studies (NIS), patient and product registries to generate RWE, but increasingly the industry is coming across more ‘pragmatic studies’. So, why is interest growing in discussion around this ‘new’ type of study?

RWE is a broad area including clinical, economic, and patient reported outcomes, epidemiological and comparative setups, and various external stakeholders as well as the manufacturer’s internal organization. Within the RWE area, comparing products’ performance in the real world has been receiving special attention: Relative or comparative effectiveness and benefit/risk are key words in today’s conferences and communication.

HTA agencies specifically look into comparative RWE: Observational methods cannot fully eliminate allocation bias, as treatments are assigned at the discretion of the treating physician. Agencies thus look to combine real world data collection with control of treatment allocation bias, preferably by study designs including subject based randomization i.e., pragmatic studies. Although the term ‘pragmatic’ has been used increasingly for such real life, randomized studies, it is not fully clear what pragmatic studies are, and for which purposes they should be performed: There are veils to lift around pragmatic studies, strategically as well as operationally.

This webinar describes and explains pragmatic studies and discusses why key Late Stage stakeholders are increasingly interested in pragmatic studies – and why, nevertheless, pragmatic approaches are still relatively rare in the area of RWE. The panel outlines operational modifications and adaptations of the main pragmatic study approach, such as community based studies, cluster randomized approaches, and ‘stepped wedge’ designs.

The panel also discusses both current and future regulatory considerations such as the new EU Clinical Trials Regulation. An outlook into the future of pragmatic study types will be provided, and strategic options for potential design modifications will be assessed. We will close our evaluation of pragmatic studies and their nuances by assessing evidence validity from pragmatic approaches with others, primarily analytic methods minimizing bias in observational settings.

Register here…

Date: Thursday, March 17, 2016Sign-Up
Time: 11am EDT (NA) / 3pm GMT (UK) / 4pm CET (EU-Central)
Duration: 60 minutes
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