SynthesisNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2025
Efficacy and safety of continuous subcutaneous ND0612 Infusion compared to oral and alternative regimens in managing motor fluctuations in Parkinson's disease: a systematic review and meta-analysis.
Synthesis in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Pooled it
- Real-world experience with foslevodopa/foscarbidopa in Germany: therapeutic insights and lessons learned.Neurological research and practice · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundContinuous subcutaneous infusion of levodopa/carbidopa (ND0612) is a promising alternative to oral therapy for Parkinson's disease. Motor fluctuations and "off time" significantly impact the quality of life in advanced diseases. This meta-analysis evaluates the effectiveness of ND0612 in reducing "off time," improving the overall quality of life, and enhancing sleep quality.
methodA comprehensive search of 549 studies was performed, and five eligible studies (n = 327) were included after intense screening. The ROB2 tool and ROBINS1 were used to assess the quality of the included studies. The outcomes assessed included reductions in "off time" (hours), quality of life (PDQ-39 scores), and sleep quality (PDSS scores). Statistical heterogeneity was assessed using the I
resultsThe meta-analysis showed a significant reduction in OFF time for ND0612 compared to oral regimens, with a standardized mean difference (SMD) of -0.53 (95% CI: -0.76, -0.30), and compared to placebo with an SMD of -0.30 (95% CI: -1.05, 0.44). For improvement in quality of life, a favorable effect of ND0612 was shown compared to oral regimens (SMD = -0.31, 95% CI: -0.54, -0.08) and placebo (SMD = 0.44, 95% CI: 1.19, -0.32). Sleep quality (PDSS scores) demonstrated a slight improvement compared with oral regimens (SMD = -0.21, 95% CI: -0.44, 0.02) and a more significant improvement compared with placebo (SMD = -0.42, 95% CI: -0.87, 0.03). Overall, ND0612 provided consistent benefits in reducing OFF time and enhancing both quality of life and sleep in patients with Parkinson's disease.
conclusionND0612 significantly reduced "off time" and improved quality of life among Parkinson's disease patients experiencing motor fluctuations. However, its effect on sleep quality was inconsistent, with no clear, robust benefit demonstrated. Overall, this analysis supports ND0612 as an effective therapeutic option in patients with advanced Parkinson's disease.
Indexed as
Identifiers
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.