NeuroDerm Ltd. clinical trials
Acquired by Tanabe Pharma Corporation, Oct 18, 2017 · source ↗
The registry lists 14 studies whose lead sponsor is NeuroDerm Ltd.. 0 are recruiting or about to start. Per ClinicalTrials.gov, last updated Jul 9, 2026.
Before and after it joined Tanabe Pharma Corporation
- First submitted before NeuroDerm Ltd. became part of Tanabe Pharma Corporation
- 12
- First submitted after NeuroDerm Ltd. became part of Tanabe Pharma Corporation
- 2
- Unclear, or no submission date
- 0
By the date each study was first submitted to the registry. The registry lists today's sponsor name and keeps no history, so this says when a study was filed, not who filed it.
Registry sponsor names on this page
- NeuroDerm Ltd.14 studies
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Studies
Recruiting first, then most recently updated. Showing 14 of 14. All Tanabe Pharma Corporation studies →
- A Safety, Tolerability and Levodopa Pharmacokinetics Study of Repeated ND0612 in Parkinson's Disease PatientsCompletedNCT01883505Phase 2
Sponsor listed in the registry: NeuroDerm Ltd. · First submitted before NeuroDerm Ltd. became part of Tanabe Pharma Corporation
- A Long Term Safety Study of ND0612 Administered as a Continuous SC Infusion in Advanced Parkinson's DiseaseActive, not recruitingNCT02726386Phase 2
Sponsor listed in the registry: NeuroDerm Ltd. · First submitted before NeuroDerm Ltd. became part of Tanabe Pharma Corporation
- Efficacy, Safety and Tolerability Study of ND0612 vs. Oral Immediate Release Levodopa/Carbidopa (IR-LD/CD) in Subjects With Parkinson's Disease Experiencing Motor FluctuationsActive, not recruitingNCT04006210Phase 3
Sponsor listed in the registry: NeuroDerm Ltd. · First submitted after NeuroDerm Ltd. became part of Tanabe Pharma Corporation
- A Safety, Tolerability, and Plasma Concentration Study of Levodopa/Carbidopa Subcutaneous Solution (ND0612) in Parkinson's Disease (PD) PatientsCompletedNCT01725802Phase 1
Sponsor listed in the registry: NeuroDerm Ltd. · First submitted before NeuroDerm Ltd. became part of Tanabe Pharma Corporation
- A Safety, Tolerability, and Pharmacokinetic Study of ND0612 Delivered as a Continuous Subcutaneous in Parkinson's Disease PatientsCompletedNCT02096601Phase 1
Sponsor listed in the registry: NeuroDerm Ltd. · First submitted before NeuroDerm Ltd. became part of Tanabe Pharma Corporation
- A Sequential Two-Part, Open-Label Study in Healthy Male and Female SubjectsCompletedNCT02604914Phase 1
Sponsor listed in the registry: NeuroDerm Ltd. · First submitted before NeuroDerm Ltd. became part of Tanabe Pharma Corporation
- Study of Subcutaneous Continuous Administration of Levodopa/Carbidopa Solution (ND0612) in Healthy VolunteersCompletedNCT01486628Phase 1
Sponsor listed in the registry: NeuroDerm Ltd. · First submitted before NeuroDerm Ltd. became part of Tanabe Pharma Corporation
- A Clinical Study of Efficacy, Safety, Tolerability and PK of ND0612H in Subjects With Advanced Parkinson's DiseaseCompletedNCT02577523Phase 2
Sponsor listed in the registry: NeuroDerm Ltd. · First submitted before NeuroDerm Ltd. became part of Tanabe Pharma Corporation
- A Clinical Study Investigating the Efficacy, Tolerability, and Safety of Continuous Subcutaneous ND0612 Infusion Given as Adjunct Treatment to Oral Levodopa in Patients With Parkinson's Disease With Motor FluctuationsWithdrawnNCT02782481Phase 3
Sponsor listed in the registry: NeuroDerm Ltd. · First submitted before NeuroDerm Ltd. became part of Tanabe Pharma Corporation
- A Study of ND0801 in Attention Deficit/Hyperactivity Disorder (ADHD)CompletedNCT01174355Phase 1/2
Sponsor listed in the registry: NeuroDerm Ltd. · First submitted before NeuroDerm Ltd. became part of Tanabe Pharma Corporation
- A Study in Patients With Advanced Parkinson's Disease to Assess the Relative Bioavailability of Levodopa Administered as ND0612 Subcutaneous Infusion Versus Levodopa Administered as Carbidopa-Levodopa Enteral SuspensionWithdrawnNCT03462043Phase 3
Sponsor listed in the registry: NeuroDerm Ltd. · First submitted after NeuroDerm Ltd. became part of Tanabe Pharma Corporation
- A Single Period Investigation to Assess the Tolerability of Healthy Subjects to Oral Sinemet® (Levodopa/Carbidopa)CompletedNCT02486432Phase 1
Sponsor listed in the registry: NeuroDerm Ltd. · First submitted before NeuroDerm Ltd. became part of Tanabe Pharma Corporation
- A Safety, Tolerability and Pharmacokinetic Study of ND0611 on the Top of Different Oral Dosage Forms of Levodopa/Carbidopa in Parkinson's Disease PatientsCompletedNCT01229332Phase 1/2
Sponsor listed in the registry: NeuroDerm Ltd. · First submitted before NeuroDerm Ltd. became part of Tanabe Pharma Corporation
- Safety, Tolerability and Pharmacokinetic Profile of Levodopa Administered With Continuous Administration of ND0611CompletedNCT01103011Phase 1
Sponsor listed in the registry: NeuroDerm Ltd. · First submitted before NeuroDerm Ltd. became part of Tanabe Pharma Corporation