Double-Blind, Randomized,Placebo-ControlledTrial ofDA-9701 in Parkinson's Disease:PASS-GIStudy
- Authors
- Choi, Ji-Hyun; Lee, Jee-Young; Cho, Jin Whan; Koh, Seong-Beom; Yang, Young Soon; Yoo, Dalla; Shin, Cheol-Min; Kim, Hee Tae
- Issue Date
- 11월-2020
- Publisher
- WILEY
- Keywords
- DA-9701; double-blind randomized controlled trial; gastrointestinal dysfunction; Parkinson' s disease; quality of life
- Citation
- MOVEMENT DISORDERS, v.35, no.11, pp.1966 - 1976
- Indexed
- SCIE
SCOPUS
- Journal Title
- MOVEMENT DISORDERS
- Volume
- 35
- Number
- 11
- Start Page
- 1966
- End Page
- 1976
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/130399
- DOI
- 10.1002/mds.28219
- ISSN
- 0885-3185
- Abstract
- Objectives This study aimed to assess the efficacy of DA-9701 on gastrointestinal symptom-related quality of life in patients with Parkinson's disease on stable dopaminergic medications. Methods This multicenter, double-blind, placebo-controlled, phase 4 trial included a total of 144 patients with Parkinson's disease with gastrointestinal dysfunctions based on predefined criteria. Participants were randomized to take either DA-9701 or placebo for 4 weeks, and then both groups were administered DA-9701 for an additional 8 weeks while antiparkinsonian medications were unchanged. The primary outcome measure was gastrointestinal symptoms and related quality-of-life changes assessed on the Korean Nepean dyspepsia index after 4 and 12 weeks of therapy. We also evaluated the impact of DA-9701 therapy on parkinsonian motor symptoms at each time point. Results The gastrointestinal symptom-related quality-of-life score significantly improved in the DA-9701-treated group compared with the placebo-treated group after 4weeks (adjustedP= 0.012 by linear mixed effect model analysis). The overall gastrointestinal symptom and dyspepsia sum scores improved at 12 weeks after intervention in the DA-9701-first treated group (adjustedP= 0.002 and 0.014, respectively) and also in the placebo-first treated group (adjustedP= 0.019 and 0.039) compared with the baseline. Parkinsonian motor severity was not significantly affected by DA-9701 treatment in both groups at 4 and 12 weeks after intervention. There were no drug-related serious adverse events throughout the trial. Conclusions DA-9701 therapy improved gastrointestinal symptom-related quality of life, and 12 weeks of daily administration can relieve the overall severity of gastrointestinal symptoms in patients with Parkinson's disease without affecting motor symptoms. (Clinical trial identifier: NCT02775591.) (c) 2020 The Authors.Movement Disorderspublished by Wiley Periodicals LLC. on behalf of International Parkinson and Movement Disorder Society.
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Collections - College of Medicine > Department of Medical Science > 1. Journal Articles
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