ECTRIMS eLearning

More flexibility for future MS trials: adaptive designs
ECTRIMS Learn. Chataway J. 10/10/18; 231809; 67
Jeremy Chataway
Jeremy Chataway
Contributions
Abstract

Abstract: 67

Type: Educational Session

Abstract Category: N/A

Control of progression in progressive multiple sclerosis (MS) naturally remains a major goal, although ultimately repair and remyelination will be needed. Robust controlled and randomised trials remain the bedrock by which an intervention is judged. In the last five years many phase 2 trials have reported in this area, with four large phase 3 trials since 2016. The question arises whether this fundamental work can be done quicker and more efficiently. This presentation will look at current views over the range of adaptive concepts and how they could be applied to future progressive MS trials.
Disclosure: The author has received support from the Efficacy and Mechanism Evaluation Programme and Health Technology Assessment Programme (NIHR); UK Multiple Sclerosis Society and National Multiple Sclerosis Society. In the last 3 years, he has been a local principal investigator for trials in multiple sclerosis funded by Receptos, Novartis, and Biogen Idec, and has received an investigator grant from Novartis outside this work. He has taken part in advisory boards/consultancy for Roche, Merck KGaA Germany, MedDay,Biogen, and Apitope.

Abstract: 67

Type: Educational Session

Abstract Category: N/A

Control of progression in progressive multiple sclerosis (MS) naturally remains a major goal, although ultimately repair and remyelination will be needed. Robust controlled and randomised trials remain the bedrock by which an intervention is judged. In the last five years many phase 2 trials have reported in this area, with four large phase 3 trials since 2016. The question arises whether this fundamental work can be done quicker and more efficiently. This presentation will look at current views over the range of adaptive concepts and how they could be applied to future progressive MS trials.
Disclosure: The author has received support from the Efficacy and Mechanism Evaluation Programme and Health Technology Assessment Programme (NIHR); UK Multiple Sclerosis Society and National Multiple Sclerosis Society. In the last 3 years, he has been a local principal investigator for trials in multiple sclerosis funded by Receptos, Novartis, and Biogen Idec, and has received an investigator grant from Novartis outside this work. He has taken part in advisory boards/consultancy for Roche, Merck KGaA Germany, MedDay,Biogen, and Apitope.

By clicking “Accept Terms & all Cookies” or by continuing to browse, you agree to the storing of third-party cookies on your device to enhance your user experience and agree to the user terms and conditions of this learning management system (LMS).

Cookie Settings
Accept Terms & all Cookies