| Literature DB >> 33442579 |
Diane Stephenson1, Robert Alexander2, Varun Aggarwal1, Reham Badawy3, Lisa Bain4, Roopal Bhatnagar1, Bastiaan R Bloem5, Babak Boroojerdi6, Jackson Burton1, Jesse M Cedarbaum1,7, Josh Cosman8,9, David T Dexter10, Marissa Dockendorf11, E Ray Dorsey12, Ariel V Dowling2, Luc J W Evers5, Katherine Fisher8, Mark Frasier13, Luis Garcia-Gancedo14, Jennifer C Goldsack15, Derek Hill1, Janice Hitchcock1, Michele T Hu16, Michael P Lawton1, Susan J Lee11, Michael Lindemann17, Ken Marek18, Nitin Mehrotra11, Marjan J Meinders5, Michael Minchik1, Lauren Oliva8, Klaus Romero1, George Roussos1,19, Robert Rubens2, Sakshi Sadar1, Joseph Scheeren1, Eiichi Sengoku6, Tanya Simuni20, Glenn Stebbins21, Kirsten I Taylor17,22, Beatrice Yang23, Neta Zach2.
Abstract
Innovative tools are urgently needed to accelerate the evaluation and subsequent approval of novel treatments that may slow, halt, or reverse the relentless progression of Parkinson disease (PD). Therapies that intervene early in the disease continuum are a priority for the many candidates in the drug development pipeline. There is a paucity of sensitive and objective, yet clinically interpretable, measures that can capture meaningful aspects of the disease. This poses a major challenge for the development of new therapies and is compounded by the considerable heterogeneity in clinical manifestations across patients and the fluctuating nature of many signs and symptoms of PD. Digital health technologies (DHT), such as smartphone applications, wearable sensors, and digital diaries, have the potential to address many of these gaps by enabling the objective, remote, and frequent measurement of PD signs and symptoms in natural living environments. The current climate of the COVID-19 pandemic creates a heightened sense of urgency for effective implementation of such strategies. In order for these technologies to be adopted in drug development studies, a regulatory-aligned consensus on best practices in implementing appropriate technologies, including the collection, processing, and interpretation of digital sensor data, is required. A growing number of collaborative initiatives are being launched to identify effective ways to advance the use of DHT in PD clinical trials. The Critical Path for Parkinson's Consortium of the Critical Path Institute is highlighted as a case example where stakeholders collectively engaged regulatory agencies on the effective use of DHT in PD clinical trials. Global regulatory agencies, including the US Food and Drug Administration and the European Medicines Agency, are encouraging the efficiencies of data-driven engagements through multistakeholder consortia. To this end, we review how the advancement of DHT can be most effectively achieved by aligning knowledge, expertise, and data sharing in ways that maximize efficiencies.Entities:
Keywords: Collaboration; Consensus; Device agnostic; Digital health technologies; Public-private partnerships; Regulatory science
Year: 2020 PMID: 33442579 PMCID: PMC7768153 DOI: 10.1159/000512500
Source DB: PubMed Journal: Digit Biomark ISSN: 2504-110X