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dc.contributor.authorKim, J-M
dc.contributor.authorChung, SJ
dc.contributor.authorKim, JW
dc.contributor.authorJeon, BS
dc.contributor.authorSingh, P
dc.contributor.authorThierfelder, S
dc.contributor.authorIkeda, J
dc.contributor.authorBauer, L
dc.contributor.authorAsia Pacific Rotigotine Add-on Study Group,
dc.date.accessioned2020-12-21T03:01:40Z
dc.date.available2020-12-21T03:01:40Z
dc.date.issued2015-02-28
dc.identifierpii: 10.1186/s12883-015-0267-7
dc.identifier.citationKim, J. -M., Chung, S. J., Kim, J. W., Jeon, B. S., Singh, P., Thierfelder, S., Ikeda, J., Bauer, L. & Asia Pacific Rotigotine Add-on Study Group, (2015). Rotigotine transdermal system as add-on to oral dopamine agonist in advanced Parkinson's disease: an open-label study.. BMC Neurol, 15 (1), pp.17-. https://doi.org/10.1186/s12883-015-0267-7.
dc.identifier.issn1471-2377
dc.identifier.urihttp://hdl.handle.net/11343/257041
dc.description.abstractBACKGROUND: Achieving optimal symptom control with minimal side effects is a major goal in clinical practice. Dual-agent dopamine receptor agonist (DA) therapy in Parkinson's disease (PD) may represent a promising approach to treatment, as the combination of different pharmacokinetic/pharmacological profiles may result in a lesser need for high dosages and, accordingly, may be well tolerated. The objective of the current study was to investigate safety and efficacy of rotigotine transdermal system as add-on to oral DA in patients with advanced PD inadequately controlled with levodopa and low-dose oral DA. METHODS: PD0015 was an open-label, multinational study in patients with advanced-PD and sleep disturbance or early-morning motor impairment. Patients were titrated to optimal dose rotigotine (≤8 mg/24 h) over 1-4 weeks and maintained for 4-7 weeks (8-week treatment). Dosage of levodopa and oral DA (pramipexole ≤1.5 mg/day, ropinirole ≤6.0 mg/day) was stable. Primary variable was Clinical Global Impressions (CGI) item 4: side effects, assessing safety. Other variables included adverse events (AEs), Patient Global Impressions of Change (PGIC), Unified Parkinson's Disease Rating Scale (UPDRS) II and III, Parkinson's Disease Sleep Scale (PDSS-2), Pittsburgh Sleep Quality Index (PSQI), and "off" time. RESULTS: Of 90 patients who received rotigotine, 79 (88%) completed the study; 5 (6%) withdrew due to AEs. Most (83/89; 93%) had a CGI-4 score <3 indicating that rotigotine add-on therapy did not interfere with functioning; 6 (7%) experienced drug-related AEs that interfered with functioning (score ≥3). AEs occurring in ≥5% were application site pruritus (13%), dizziness (10%), orthostatic hypotension (10%), nausea (8%), dyskinesia (8%), and nasopharyngitis (6%). Numerical improvements in motor function (UPDRS III), activities of daily living (UPDRS II), sleep disturbances (PDSS-2, PSQI), and reduction in "off" time were observed. The majority (71/88; 81%) improved on PGIC. CONCLUSIONS: Addition of rotigotine transdermal system to low-dose oral DA in patients with advanced-PD was feasible and may be associated with clinical benefit. TRIAL REGISTRATION: ClinicalTrials.gov identifier NCT01723904 . Trial registration date: November 6, 2012.
dc.languageeng
dc.publisherSpringer Science and Business Media LLC
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.titleRotigotine transdermal system as add-on to oral dopamine agonist in advanced Parkinson's disease: an open-label study.
dc.typeJournal Article
dc.identifier.doi10.1186/s12883-015-0267-7
melbourne.affiliation.departmentMedicine (RMH)
melbourne.affiliation.facultyMedicine, Dentistry & Health Sciences
melbourne.source.titleBMC Neurology
melbourne.source.volume15
melbourne.source.issue1
melbourne.source.pages17-
dc.rights.licenseCC BY
melbourne.elementsid1236727
melbourne.openaccess.pmchttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364324
melbourne.contributor.authorEvans, Andrew
dc.identifier.eissn1471-2377
melbourne.accessrightsOpen Access


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