Study to Assess Pharmacokinetics of Accordion Pill Carbidopa-Levodopa Compared to Immediate Release Carbidopa-Levodopa in Parkinson's Disease Patients

Parkinson Disease Clinical Trial

Official title:

An Open Label Phase 2 Study to Assess the Pharmacokinetics of the Accordion Pill Carbidopa-Levodopa Compared to Immediate Release Carbidopa-Levodopa in Patients With Parkinson's Disease

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03576638
• Other study ID #: IN 18001
• Secondary ID: 2018-001209-95
• Status: Not yet recruiting
• Phase: Phase 2
• Start date: July 2018
• Est. completion date: January 2019

Study information

• Verified date: June 2018
• Source: Intec Pharma Ltd.
• Contact: Fabrizio Stocchi, MD, PhD
• Phone: +39 0652252311
• Email: fabrizio.stocchi[@]sanraffaele.it
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to assess the PK of AP-CD/LD given at dose of 50/500mg three times daily compared to CD/LD immediate release (Sinemet) 1.5 tablets of dose of 25/100 given 5 times per day in Parkinson's Disease patients.

Description:

An open label, non randomized crossover phase 2 study to assess the PK of AP-CD/LD given at dose of 50/500mg three times daily compared to CD/LD immediate release (Sinemet) 1.5 tablets of dose of 25/100 given 5 times per day in Parkinson's Disease patients. The study will have a screening period followed by an overnight stay in clinic where Immediate release CD/LD (Sinemet) will be administered five times, approximately every three hours. At specified intervals, blood will be drawn for PK testing. On Days 2-7, subjects will be treated at home with AP CD/LD three times/day, approximately every five hours. Day 8 will be overnight stay in clinic for PK study. AP CD/LD 500mg TID will be dispensed to subjects with specified timelines for PK assessment. Each subject will return to clinic on day 15 for a safety followup visit.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 12
• Est. completion date: January 2019
• Est. primary completion date: January 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 30 Years and older

Eligibility

Inclusion Criteria:

1. diagnosis of PD consistent with UK Brain Bank Criteria

2. Stable dose of levodopa/carbidopa IR for at least 4 weeks prior to entry; taking at least 4 doses of IR levodopa during waking hours, and total daily dose of at least 400mg prior to initial screening

3. Stable on all anti-PD medications for 30 days prior to screening. COMT inhibitors are held prior to PK studies on day 1 through day 8

Exclusion Criteria:

1. Atypical or secondary parkinsonism

2. clinically significant cardiac, pulmonary, hepatic, or renal disease or other condition which contraindicates participation in judgement of investigator

3. severe dyskinesia as assessed by PI

4. significant cognitive impairment

5. Clinically significant psychiatric illness in opinion of PI

6. history of small bowel or gastric surgery (including PEG-J placement for Duopa/Duodopa) or bowel obstruction, diagnosis of small bowel narrowing, diagnosis of Crohn's disease, frequent nausea or emesis regardless of etiology, and symptomatic gastroparesis.

7. History of GI pathology of clinical significance as determined by PI

8. Allergy to study drug or Yellow Dye #5 (tartrazine)

9. Unable to swallow large pills

10. Active GERD and regular use of PPIs

11. Women who are pregnant or nursing or are of childbearing potential who are not willing to use a medically acceptable method of contraception

Related Conditions & MeSH terms

• Parkinson Disease

Intervention

Drug:
• Accordion Pill Carbidopa/Levodopa
AP 50/500 TID days 2-7
• Sinemet CR 25Mg-100Mg Extended-Release Tablet
25/100 1.5 pills five times/day

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Intec Pharma Ltd.

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Variability in plasma levodopa concentration	as assessed by levodopa fluctuation index (comparison of AP-CD/LD to IR-CD/LD	Pk blood sampling to be performed time 0 and every 30 minutes for 16 hours and again at 24 hours on days 1 and 8.
Secondary	Variability in plasma levodopa concentration	as assessed by Coefficient of variation (CV) (comparison of AP-CD/LD to IR-CD/LD)	Pk blood sampling to be performed time 0 and every 30 minutes for 16 hours and again at 24 hours on days 1 and 8.