Active, not recruiting
Phase 2
A Long Term Safety Study of ND0612 Administered as a Continuous SC Infusion in Advanced Parkinson's Disease
Condition(s) studied
Parkinson's Disease
Investigational drug(s) / intervention(s)
ND0612
ND0612: ND0612, a solution of levodopa/carbidopa (LD/CD) delivered continuously subcutaneously (SC) via an infusion pump system
Study summary
This is a multi-center, international, open-label, safety study of ND0612, a solution of levodopa/carbidopa (LD/CD) delivered via a pump system as a continuous SC infusion in subjects with advanced Parkinson's Disease (PD).
Eligibility
INCLUSION CRITERIA:
Cohort 1.
1. Subject is able to, and has signed an Institutional Review Board/Ethics Committee (IRB/EC)-approved informed consent form (ICF).
2. Subject has completed the treatment period of study ND0612H-006 not more than one month prior to enrolling in ND0612H-012.
3. Willing and able to administer the SC infusion alone or with the assistance of a study partner and able to comply with the study specific procedures.
Cohort 2.
1. Male and female PD subjects of any race aged at least 30 years who sign an IRB/EC-approved ICF.
2. PD diagnosis consistent with the UK Brain Bank Criteria.
3. Modified Hoehn \& Yahr scale in "ON" state of stage ≤3.
4. Taking at least 4 doses/day of LD/DDI (or at least 3 doses/day of Rytary) and taking, or have attempted to take, at least one other PD treatment for at least 30 days.
5. Subjects must be stable on their anti-PD medications for at least 30 days before Day 1.
6. Subjects may have had prior exposure to SC apomorphine injections/infusion but must have stopped continuous apomorphine administration at least 4 weeks before the screening visit. Treatment with apomorphine is prohibited during the entire ND0612 treatment period.
7. Must have a minimum of 2 hrs of "OFF" time per day with predictable early morning "OFF" periods as estimated by the subject.
8. 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.
9. Mini Mental State Examination (MMSE) score ≥26.
10. No clinically significant medical, psychiatric or laboratory abnormalities which the investigator judges would be unsafe or non-compliant in the study.
11. Female subjects must be surgically sterile (hysterectomy, bilateral oophorectomy, or tubal ligation), 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, 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. Alternatively, true abstinence is acceptable when it is in line with the subject's preferred and usual lifestyle. If a subject is usually not sexually active but becomes active, the subject and sexual partner must comply with the contraceptive requirements detailed above.
12. Willing and able to administer the SC infusion alone or with the assistance of a study partner after a screening period of up to 40 days and willing and able to comply with study requirements.
13. Subjects should have a named study partner.
EXCLUSION CRITERIA:
Cohort 1 and 2. Previously unable to tolerate ND0612 and/or have experienced intolerable adverse drug reactions associated with its use, regardless of the dosing regimen administered.
Cohort 2.
1. Atypical or secondary parkinsonism.
2. Acute psychosis or hallucinations in past 6 months.
3. Any relevant medical, surgical, or psychiatric condition, laboratory value, or concomitant medication which, in the opinion of the Investigator makes the subject unsuitable for study entry or potentially unable to complete all aspects of the study.
4. Any malignancy in the 5 years prior to randomization (excluding basal cell carcinoma of the skin or cervical carcinoma in situ that have been successfully treated).
5. Positive serum serology for Hepatitis B Virus (HBV), Hepatitis C Virus (HCV) or Human Immunodeficiency Virus (HIV) at the Screening visit.
6. Prior neurosurgical procedure for PD, or Duodopa treatment
7. Subjects with a history of drug abuse or alcoholism within the past 12 months.
8. Clinically significant ECG rhythm abnormalities.
9. 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.
10. Current participation in a clinical trial with an investigational product or past participation within the last 30 days before Day 1.
Primary outcome measure(s)
- Adverse Events (Long-term Safety) — Baseline to Month 12
Long-term safety (systemic and local) assessment will be based on adverse events (AEs), with a focus on adverse events of special interest (AESI), i.e., infusion site reactions, cases of hypersensitivity, polyneuropathy.
- Percentages of Subjects Who Complete the 12-month Treatment Period or Discontinue Due to AE (Tolerability) — Baseline to Month 12
Tolerability will be assessed based on the percentage of subjects that complete the 12-month treatment period of the study and the percentage of subjects who discontinue from the 12-month treatment period due to an AE.
Trial sites (57)
| Facility | City | Region | Status |
| Xenoscience |
Phoenix |
Arizona |
|
| Clinical Trials Inc. |
Little Rock |
Arkansas |
|
| The Parkinsons and Movement Disorder Institute |
Fountain Valley |
California |
|
| Neuro Pain Medical Center |
Fresno |
California |
|
| University of Colorado Denver |
Aurora |
Colorado |
|
| Rocky Mountain Movement Disorders Center |
Englewood |
Colorado |
|
| Parkinson's Disease and Movement Disorder Center of Boca Raton |
Boca Raton |
Florida |
|
| MD Clinical |
Hallandale |
Florida |
|
| Infinity Clinical Research, LLC |
Hollywood |
Florida |
|
| University of Florida Health at Jacksonville |
Jacksonville |
Florida |
|
| Neurology Associates, PA |
Maitland |
Florida |
|
| Parkinsons Disease Treatment Center of Southwest Florida |
Port Charlotte |
Florida |
|
| Suncoast Neuroscience Associates |
St. Petersburg |
Florida |
|
| Infinity Clinical Research, LLC |
Sunrise |
Florida |
|
| USF Health Parkinson's Disease and Movement Disorders |
Tampa |
Florida |
|
| Northwestern University |
Chicago |
Illinois |
|
| Unity Point Health |
Des Moines |
Iowa |
|
| University of Maryland, Neurology |
Baltimore |
Maryland |
|
| QUEST Research Institute |
Farmington Hills |
Michigan |
|
| Henry Ford Hospital |
West Bloomfield |
Michigan |
|
| Pyramid Clinical Research |
Somerset |
New Jersey |
|
| University of Cincinnati |
Cincinnati |
Ohio |
|
| The Movement Disorder Clinic of Oklahoma |
Tulsa |
Oklahoma |
|
| Synergy Trials |
Richmond |
Virginia |
|
| Sentara Neuroscience Institute |
Virginia Beach |
Virginia |
|
| Premier Research |
Spokane |
Washington |
|
| Medical University Innsbruck |
Innsbruck |
Austria |
|
| NEUROHK, s.r.o. |
Choceň |
Czechia |
|
| Clintrial s.r.o. |
Prague |
Czechia |
|
| Vestra Clinics, s.r.o. |
Rychnov nad Kněžnou |
Czechia |
|
| Centre Hospitalier d'Aix |
Aix-en-Provence |
France |
|
| CHU d'Amiens, Hopital Sud |
Amiens |
France |
|
| Hopital Neurologique Pierre Wertheimer |
Bron |
France |
|
| Hôpital Gabriel Montpied |
Clermont-Ferrand |
France |
|
| Hopital Roger Salengro |
Lille |
France |
|
| Hopital de la Timone |
Marseille |
France |
|
| CHU de Poitiers |
Poitiers |
France |
|
| Kliniken Beelitz GmbH |
Beelitz-Heilstätten |
Germany |
|
| St. Josefs Hospital |
Bochum |
Germany |
|
| Klinikum-Bremerhaven Reinkenheide |
Bremerhaven |
Germany |
|
+ 17 more sites — see the full list on the official registry below.
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