A Clinical Study of Efficacy, Safety, Tolerability and PK of ND0612H in Subjects With Advanced Parkinson's Disease

Completed · Phase 2

Conditions studied: Parkinson's Disease

In brief

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.

Key facts

Study ID

NCT02577523

Run by

NeuroDerm Ltd.

People needed

38

Starts

2015-12-29

Expected to finish

2017-01-31

Last updated by the study team

2023-05-25

Who can join

Age: 30 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• 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.

Where it is running

• Northwestern University — Chicago, Illinois, United States
• QUEST Research Institute — Farmington Hills, Michigan, United States
• University of Cincinnati — Cincinnati, Ohio, United States
• Medical University Innsbruck — Innsbruck, Austria
• Rabin Medical Center — Petah Tikva, Israel
• Chaim Sheba Medical Center — Ramat Gan, Israel
• Sourasky Medical Center — Tel Aviv, Israel
• University Foundation — Chieti, Italy
• AOU Pisa — Pisa, Italy
• IRCCS San Raffaele Pisana — Rome, Italy
• Fondazione Ospedale San Camillo - I.R.C.C.S. — Venice, Italy

Full record on ClinicalTrials.gov

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