Taylor Kirsten I, Lipsmeier Florian, Scelsi Marzia A, Volkova-Volkmar Ekaterina, Rukina Daria, Popp Werner, Lambrecht Stefan, Anzures-Cabrera Judith, Summers David, Abt Markus, Monnet Annabelle, Kilchenmann Timothy, Schjodt-Eriksen Jens, Essioux Laurent, Kustermann Thomas, Zago Wagner, Svoboda Hanno, Nikolcheva Tania, Postuma Ronald B, Pagano Gennaro, Lindemann Michael
Roche Pharma Research and Early Development (pRED) Neuroscience & Rare Diseases, Data & Analytics, Pharmaceutical Sciences, Clinical Pharmacology, Roche Innovation Center Basel, F. Hoffmann-La Roche Ltd., Basel, Switzerland.
Roche Information Solutions (RIS) Data & Analytics, Roche Diagnostics, F. Hoffmann-La Roche Ltd., Basel, Switzerland.
NPJ Digit Med. 2025 Jun 16;8(1):365. doi: 10.1038/s41746-025-01572-8.
Digital health technology (DHT) tools for Parkinson's disease (PD) e.g., smartphones and wearables were used for remote and frequent measurement of motor signs in the phase 2 PASADENA study of the anti-alpha-synuclein monoclonal antibody prasinezumab. 316 early-stage PD participants were randomized to placebo, 1500 mg, or 4500 mg prasinezumab for 52 weeks; placebo participants were re-randomized to prasinezumab for the ensuing 52 weeks. Patients performed daily smartphone motor "active tests", and were passively monitored by smartphone/smartwatch throughout the day over 2 y. Change from baseline analyses censored data at dopaminergic treatment start. Bilateral speeded tapping variability and hand-turning, U-turn speed, passively monitored hand movement power, and summary Simple Sum scores progressed numerically less in prasinezumab-treated vs placebo at week 52. All findings except hand-turning persisted at week 104. DHT sensor-based outcome measures may contribute to quantifying disease progression in clinical research of early-stage, dopaminergic treatment-naïve PD. Clinical Trial Registry Name: ClinicalTrials.gov; Clinical Trial Registry ID: NCT03100149; registered 2017-03-29.
在抗α-突触核蛋白单克隆抗体普拉克索单抗的2期帕萨迪纳研究中,用于帕金森病(PD)的数字健康技术(DHT)工具,如智能手机和可穿戴设备,被用于远程和频繁测量运动体征。316名早期PD参与者被随机分为安慰剂组、1500毫克或4500毫克普拉克索单抗组,为期52周;安慰剂组参与者在接下来的52周被重新随机分为普拉克索单抗组。患者每天进行智能手机运动“主动测试”,并在2年时间里通过智能手机/智能手表进行全天被动监测。从基线分析开始,在多巴胺能治疗开始时对删失数据进行分析。在第52周时,与安慰剂组相比,普拉克索单抗治疗组的双侧快速敲击变异性和手部转动、掉头速度、被动监测的手部运动力量以及简易总和评分的数值进展较小。除手部转动外,所有结果在第104周时仍然存在。基于DHT传感器的结局指标可能有助于在早期、未接受多巴胺能治疗的PD临床研究中量化疾病进展。临床试验注册名称:ClinicalTrials.gov;临床试验注册号:NCT03100149;注册时间:2017年3月29日。