A Clinical Study Investigating the Efficacy, Safety, Tolerability and Pharmacokinetics of ND0612H, a Solution of Levodopa/Carbidopa Administered as a Continuous Subcutaneous Infusion in Subjects With Advanced Parkinson's Disease
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| ClinicalTrials.gov Identifier: NCT02577523 |
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Recruitment Status : Unknown
Verified May 2016 by NeuroDerm Ltd..
Recruitment status was: Active, not recruiting
First Posted : October 16, 2015
Last Update Posted : January 5, 2017
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Sponsor:
NeuroDerm Ltd.
Information provided by (Responsible Party):
NeuroDerm Ltd.
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Brief Summary:
This is a multicenter, parallel-group, rater-blinded, randomized clinical study in subjects with advanced PD investigating the efficacy, PK, safety and tolerability of continuous SC infusion of 2 dosing regimens of ND0612H, a solution of LD/CD delivered via a pump system as a continuous SC infusion, compared to standard oral LD/CD. After screening, subjects will undergo 1 day of standard oral LD/CD inpatient dosing followed by 2 days of inpatient treatment with 1 of 2 randomly allocated (1:1 randomization ratio) dosing regimens of ND0612H continuous SC infusion. Subjects will then continue on a maintenance dose of the assigned ND0612H dosing regimen for the next 25 days. A safety visit will be performed 4 weeks after the last SC administration of the study drug for a total of about 2.5 months of participation for each subject enrolled into the trial.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Parkinson's Disease | Drug: ND0612 (Levodopa/Carbidopa solution) | Phase 2 |
This phase IIa randomized, controlled, parallel-group study will be conducted in 36 subjects with advanced PD who are treated with oral LD/CD at a stable dose and have predictable morning "OFF" periods and at least 2.5 hrs of daily "OFF" periods. The study will investigate the efficacy, PK, safety and tolerability of continuous SC infusion of 2 dosing regimens of ND0612H. Regimen 1 will employ continuous infusion for 24 hrs using a low infusion rate at night and a higher rate at daytime with supplemental administration of oral immediate release (IR) LD/CD in the mornings. During the inpatient period of about 3 days, the site staff will manage the administration and replacement of the infusions. On Day 4 subjects will be discharged home after they and their study partners have received training on the administration of the infusion. A safety visit will be performed 4 weeks after the last SC administration of the study drug.
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 38 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Single (Outcomes Assessor) |
| Primary Purpose: | Treatment |
| Official Title: | A Multicenter, Parallel-group, Rater-blinded, Randomized Clinical Study Investigating the Efficacy, Safety, Tolerability and Pharmacokinetics of 2 Dosing Regimens of ND0612H, a Solution of Levodopa/Carbidopa Delivered Via a Pump System as a Continuous Subcutaneous Infusion in Subjects With Advanced Parkinson's Disease |
| Study Start Date : | November 2015 |
| Actual Primary Completion Date : | December 2016 |
| Estimated Study Completion Date : | March 2017 |
Resource links provided by the National Library of Medicine
Genetics Home Reference related topics:
Parkinson disease
MedlinePlus related topics:
Parkinson's Disease
| Arm | Intervention/treatment |
|---|---|
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Experimental: ND0612 (Levodopa/Carbidopa solution) Dosing Regimen 1
Dosing Regimen 1 of ND0612 (Levodopa/Carbidopa solution) continuous SC infusion over 24 hours
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Drug: ND0612 (Levodopa/Carbidopa solution) |
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Experimental: ND0612 (Levodopa/Carbidopa solution) Dosing Regimen 2
Dosing Regimen 2 of ND0612 (Levodopa/Carbidopa solution) continuous SC infusion over 14 hours
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Drug: ND0612 (Levodopa/Carbidopa solution) |
Primary Outcome Measures :
- Change from baseline to Day 28 in daily "OFF" time [ Time Frame: Baseline to Day 28 ]
Information from the National Library of Medicine
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| Ages Eligible for Study: | 30 Years to 80 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Male and female PD subjects of any race aged 30 to 80 years who sign an Institutional Review Board/Ethics Committee (IRB/EC)-approved informed consent form (ICF).
- PD diagnosis consistent with the UK Brain Bank Criteria.
- Modified Hoehn & Yahr scale in "ON" state of stage ≤3.
- Taking at least 4 doses/day of LD (or at least 3 doses/day of Rytary) and taking, or have attempted to take, at least 2 other classes of anti-PD medications in a therapeutic dose for at least 30 consecutive days each.
- Subjects must be stable on their anti-PD medications for at least 30 days before Day 1.
- Subjects may have had prior exposure to SC apomorphine injections/infusion but must have stopped administration at least 4 weeks before the screening visit. Treatment with apomorphine is prohibited during the entire ND0612H treatment period.
- Must have a minimum of 2.5 hrs of "OFF" time per day with predictable early morning "OFF" periods as estimated by the subject.
- Must have predictable and well defined early morning "OFF" periods with a good response to LD for treatment of the early morning "OFF" in the judgement of the investigator.
- Mini Mental State Examination (MMSE) score >26.
- No clinically significant medical, psychiatric or laboratory abnormalities which the investigator judges would be unsafe or non-compliant in the study.
- Female subjects must be surgically sterile, postmenopausal (defined as cessation of menses for at least 1 year), or willing to practice a highly effective method of contraception. All female participants must be non-lactating and non-pregnant and have a negative urine pregnancy test at Screening and at Baseline. Female subjects of childbearing potential must practice a highly effective method of contraception (e.g., oral contraceptives, a barrier method of birth control [e.g., condoms with contraceptive foams, diaphragms with contraceptive jelly], intrauterine devices, partner with vasectomy), 1 month before enrollment, for the duration of the study, and 3 months after the last dose of study drug.
- Willingness and ability to comply with study requirements
Exclusion Criteria:
- Atypical or secondary parkinsonism.
- Acute psychosis or hallucinations in past 6 months.
- Any relevant medical, surgical, or psychiatric condition, laboratory value, or concomitant medication which, in the opinion of the Investigator or the eligibility reviewer, makes the subject unsuitable for study entry or potentially unable to complete all aspects of the study.
- Prior neurosurgical procedure for PD, or duodopa treatment.
- Subjects with a history of drug abuse or alcoholism within the past 12 months.
- Clinically significant ECG rhythm abnormalities.
- Renal or liver dysfunction that may alter drug metabolism including: serum creatinine >1.3 mg/dL, serum aspartate aminotransferase (AST) or alanine aminotransferase (ALT) >2 x upper limit of normal (ULN), total serum bilirubin >2.5 mg/dL.
- Subjects who are not willing to operate the pump system.
Information from the National Library of Medicine
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02577523
Locations
| United States, Illinois | |
| Northwestern University | |
| Chicago, Illinois, United States, 60611 | |
| United States, Michigan | |
| QUEST Research Institute | |
| Farmington Hills, Michigan, United States, 48334 | |
| Austria | |
| Medical University Innsbruck | |
| Innsbruck, Austria, A- 4060 | |
| Israel | |
| Rabin Medical Center | |
| Petah Tikva, Israel, 4941492 | |
| Chaim Sheba Medical Center | |
| Ramat Gan, Israel, 56520 | |
| Sourasky Medical Center | |
| Tel Aviv, Israel, 64239 | |
| Italy | |
| IRCCS San Raffaele Pisana | |
| Rome, Italy, 00163 | |
| Fondazione Ospedale San Camillo - I.R.C.C.S. | |
| Venice, Italy, 30126 | |
Sponsors and Collaborators
NeuroDerm Ltd.
| Responsible Party: | NeuroDerm Ltd. |
| ClinicalTrials.gov Identifier: | NCT02577523 History of Changes |
| Other Study ID Numbers: |
ND0612H-006 |
| First Posted: | October 16, 2015 Key Record Dates |
| Last Update Posted: | January 5, 2017 |
| Last Verified: | May 2016 |
Additional relevant MeSH terms:
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Parkinson Disease Parkinsonian Disorders Basal Ganglia Diseases Brain Diseases Central Nervous System Diseases Nervous System Diseases Movement Disorders Neurodegenerative Diseases Pharmaceutical Solutions Levodopa |
Carbidopa Antiparkinson Agents Anti-Dyskinesia Agents Dopamine Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Physiological Effects of Drugs Aromatic Amino Acid Decarboxylase Inhibitors Enzyme Inhibitors |