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BouNDless: An active-controlled randomized, double-blind double-dummy study of continuous ND0612 infusion in patients with fluctuating Parkinson’s disease

W. Poewe, K. Kieburtz, F. Stocchi, S. Oren, T. Yardeni, L. Adar, O. Rosenfeld, C. Olanow (Innsbruck, Austria)

Meeting: 2019 International Congress

Abstract Number: 179

Keywords: Levodopa(L-dopa), Wearing-off fluctuations

Session Information

Date: Monday, September 23, 2019

Session Title: Clinical Trials, Pharmacology and Treatment

Session Time: 1:45pm-3:15pm

Location: Agora 3 West, Level 3

Objective: Determine the efficacy, safety, and tolerability of continuous subcutaneous ND0612 infusion in comparison to oral Carbidopa/Levodopa (CD/LD) in patients with Parkinson’s disease (PD) experiencing motor fluctuations.

Background: ND0612 is under development as the first non-surgical drug-device combination that provides continuous delivery of Carbidopa/Levodopa Subcutaneous Solution (CLSS) for patients with fluctuating PD.

Method: A total of 288 PD patients (Hoehn and Yahr ≤3) on ≥4 doses/day of CD/LD oral therapy (≥400mg of LD), experiencing motor fluctuations (average of at least 2.5 hours daily, with a minimum of 2 hours every day) in the OFF state during the waking hours) will be enrolled. The study comprises 6 periods: Period 1: Screening (1-4 weeks); Period 2: Open-label oral CD/LD adjustment period (6 weeks); Period 3: Open-label ND0612 conversion period (6 weeks); Period 4:  Double-blind, double-dummy, active-controlled, maintenance period where patients are randomized to either ND0612 infusion + Dummy IR CD/LD, OR to Dummy infusion + IR CD/LD  (12 weeks); Period 5: Optional open-label extension period (1-year); Period 6: Safety follow-up (12 weeks).

Results: The primary endpoint is the change from Baseline (start of Period 3 = start of ND0612 infusion) to end of the maintenance period (Period 4, Week 12) in mean ON time without troublesome dyskinesia, normalized to 16 waking hours, using patient-rated ON/OFF diary assessments. Secondary outcome measures include changes in: OFF time (key secondary), UPDRS (Parts II and III), Patient’s and Clinician’s Global Impressions of Change, ON time without dyskinesia, PDQ-39 and Parkinson’s Disease Sleep Scale (PDSS) scores. Clinical assessments are by blinded-rater. Safety and tolerability are assessed via adverse event reporting, including local skin safety assessments, rates of premature discontinuation, and study treatment compliance.

Conclusion: BouNDless will be the first Phase III randomized, active-controlled trial to establish the efficacy and safety of maintenance treatment with continuous subcutaneous ND0612 in comparison to oral immediate-release CD/LD in patients with PD experiencing motor fluctuations.

To cite this abstract in AMA style:

W. Poewe, K. Kieburtz, F. Stocchi, S. Oren, T. Yardeni, L. Adar, O. Rosenfeld, C. Olanow. BouNDless: An active-controlled randomized, double-blind double-dummy study of continuous ND0612 infusion in patients with fluctuating Parkinson’s disease [abstract]. Mov Disord. 2019; 34 (suppl 2). https://www.mdsabstracts.org/abstract/boundless-an-active-controlled-randomized-double-blind-double-dummy-study-of-continuous-nd0612-infusion-in-patients-with-fluctuating-parkinsons-disease/. Accessed June 14, 2025.
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