Already a DIA Member? Sign in. Not a member? Join.

Sign in

Forgot User ID? or Forgot Password?

Not a Member?

Create Account and Join

McCormick Place

Jun 18, 2017 8:30 AM - Jun 22, 2017 12:45 PM

2301 South Martin Luther King Jr. Drive, Gate 4, Chicago, IL 60616

DIA 2017 Annual Meeting

Integrating the Patient's Voice Across the Development Program of Rare Diseases: Translation Into Meaningful Outcomes

Session Chair(s)

David H. Schubert

David H. Schubert

DH Schubert Regulatory Solutions LLC, United States

Patients living with a rare disease have a direct stake in the end-benefit, and as a result should have their perspective included in the process of developing drugs. The development of clinically meaningful “patient focused” outcome measures has advanced substantially in recent decades. However, several challenges remain when designing and implementing meaningful outcome measures, including heterogeneity of outcomes, availability of suitable, reliable and valid measures, recruitment, and selection of appropriate data collection methods. This session will discuss how the inclusion of the patient's knowledge and experience, the Patient’s Voice, throughout the investigational continuum can help address the many drug development challenges, yield better clinically meaningful outcomes, and get therapies to patient's faster.

Learning Objective : Discuss the various ways of collecting data and various types of patient perspective data and how such data can be used to create patient-centered alignment on regulatory decisions regarding safety and effectiveness; Describe potential benefits and risks of integrating the patient voice throughout clinical development; Discuss examples of how patient engagement at various stages of clinical development has positively impacted clinical trials.

Speaker(s)

Lisa  Dilworth, MS

The Importance of Meaningful Endpoints for Rare Disease Clinicians and Patients

Lisa Dilworth, MS

Synteract, United States

Vice President, Rare and Orphan Diseases

Benoit  Arnould, PhD, MSc

Developing the PKU-QOL: A Long Journey to Integrate the Patients’ Voice into Phenylketonuria Drug Development Programs

Benoit Arnould, PhD, MSc

Mapi, France

Senior Director, Global, Patient-Centered Outcomes, Patient Centered Sciences

Lili  Garrard, PhD

Rare Disease Drug Development: Incorporating Patients' Perspective Through the Use of Patient Exit Interviews

Lili Garrard, PhD

FDA, United States

Mathematical Statistician, Office of Biostatistics, OTS, CDER

Have an account?

Be informed and stay engaged.

Don't miss an opportunity - join our mailing list to stay up to date on DIA insights and events.