A Sequential Two-Part, Open-Label Study in Healthy Male and Female Subjects

• Register: ClinicalTrials.gov
• Last refreshed on: 29 January 2024
• Main ID: NCT02604914
• Date of registration: 03/11/2015
• Prospective Registration: No
• Primary sponsor: NeuroDerm Ltd.
• Public title: A Sequential Two-Part, Open-Label Study in Healthy Male and Female Subjects
• Scientific title: 1) To Identify the Concentration of CD That Provides Optimal Bioavailability of a Concomitant Fixed Concentration of LD Infused SC Continuously; 2) To Compare the Bioavailability of the Optimal LD/CD Solution to That of LD/CD Intestinal Gel
• Date of first enrolment: May 29, 2015
• Target sample size: 36
• Recruitment status: Completed
• URL: https://clinicaltrials.gov/ct2/show/NCT02604914
• Study type: Interventional
• Study design: Allocation: Randomized. Intervention model: Crossover Assignment. Primary purpose: Treatment. Masking: None (Open Label).
• Phase: Phase 1

Countries of recruitment

United Kingdom

Contacts

• Name: Philip evans, MBChB, MRCS
• Affiliation: Quotient Clinical LTD

Key inclusion & exclusion criteria

Inclusion Criteria:

Inclusion Criteria: Part 1 ND0612-005a:

1. Healthy males or non-pregnant, non-lactating healthy females

2. Age 40 to 65 years of age

3. Body mass index of 18.0 to 32.0 kg/m2 or, if outside the range, considered not
clinically significant by the investigator

4. Must be willing and able to communicate and participate in the whole study (Part 1
only for subjects assigned to ND0612L and Part 1 and Part 2 for subjects assigned to
ND0612H)

5. Must provide written informed consent

6. Area of administration to be evaluable for local skin reaction (normal skin without
skin burns, scars or large tattoos in the area of administration)

7. Must agree to use an adequate method of contraception

Inclusion Criteria: Part 2 ND0612-005b:

1. Subjects who were dosed with ND0612H (any replacements subjects enrolled in Part 2 will
be dosed with the optimal LD/CD concentration of ND0612H after completion of Part 2).

Exclusion Criteria:

1. Participation in a clinical research study within the previous 3 months

2. Subjects who are study site employees, or immediate family members of a study site or
sponsor employee

3. Subjects who have previously been enrolled in this study

4. History of any drug or alcohol abuse in the past 2 years

5. Regular alcohol consumption in males >21 units per week and females >14 units per week
(1 unit = ½ pint beer, 25 mL of 40% spirit or a 125 mL glass of wine)

6. Current smokers and those who have smoked within the last 12 months. A breath carbon
monoxide reading of greater than 10 ppm at screening

7. Females of childbearing potential who are pregnant or lactating (female subjects must
have a negative urine pregnancy test at admission)

8. Clinically significant abnormal biochemistry, haematology or urinalysis as judged by
the investigator (laboratory parameters are listed in Appendix 1)

9. Positive drugs of abuse test result (drugs of abuse tests are listed in Appendix 1)

10. Positive hepatitis B surface antigen (HBsAg), hepatitis C virus antibody (HCV Ab) or
human immunodeficiency virus (HIV) results

11. Subjects who do not have suitable veins for multiple venepunctures/cannulation as
assessed by the investigator at screening

12. History of cardiovascular, renal, hepatic, chronic respiratory or GI disease as judged
by the investigator

13. Serious adverse reaction or serious hypersensitivity to any drug or the formulation
excipients

14. Presence or history of clinically significant allergy requiring treatment, as judged
by the investigator. Hayfever is allowed unless it is active

15. Donation or loss of greater than 400 mL of blood within the previous 3 months

16. Subjects who are taking, or have taken, any prescribed or over-the-counter drug (other
than 4 g per day paracetamol, hormone replacement therapy and hormonal contraception)
or herbal remedies in the 14 days before IMP administration (See Section 11.4).
Exceptions may apply on a case by case basis if considered not to interfere with the
objectives of the study as agreed by the PI and sponsor's medical monitor

17. Use of any non-selective monoamine oxidase (MAO) inhibitors within 2 weeks of
screening

18. History or presence of glaucoma

19. History or presence of suspicious undiagnosed skin lesions or a history of melanoma

20. Any history of psychoses or seizure

21. Known hypersensitivity to Sinemet® or domperidone or any of the excipients

22. Any history or presence of Prolactin-releasing pituitary tumour (prolactinoma)

23. Any medical history of GI haemorrhage, mechanical obstruction or perforation

24. Any history of moderate or severe hepatic impairment

25. Subjects with clinically significant liver function tests

26. Subjects with QTc >450 ms at screening

27. Subjects with significant electrolyte disturbances

28. Subjects with any underlying cardiac disease

29. Subjects who have received QT-prolonging drugs or potent cytochrome P450 (CYP) 3A4
inhibitors within 4 weeks of screening

30. ND0612H arm only: Subjects who have sinus problems

31. ND0612H arm only: Subjects who have regular heartburn and/or indigestion

32. ND0612H arm only: Subjects who have had abdominal (bowel) surgery

33. ND0612H arm only: Any clinically significant findings observed during naso-jejunal
tube placement as determined by the endoscopist

34. Failure to satisfy the investigator of fitness to participate for any other reason



Age minimum: 30 Years
Age maximum: 65 Years
Gender: All

Health Condition(s) or Problem(s) studied

Parkinson's Disease

Intervention(s)

Drug: LCIG

Drug: ND0612

Primary Outcome(s)

Cmax (maximal plasma concentration) of LD and CD for ND0612 vs. LCIG [Time Frame: 4 days]

AUC (area under the curve) of CD for different doses of CD [Time Frame: 6 days]

AUC (area under the curve) of LD and CD for ND0612. LCIG [Time Frame: 4 days]

Cmax (maximal plasma concentration) of CD for different doses of CD [Time Frame: 6 days]

Secondary ID(s)

ND0612-005

Source(s) of Monetary Support

Please refer to primary and secondary sponsors

Secondary Sponsor(s)

Quotient Clinical