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

PHASE2CompletedINTERVENTIONAL
Enrollment

38

Participants

Timeline

Start Date

December 29, 2015

Primary Completion Date

December 20, 2016

Study Completion Date

January 31, 2017

Conditions
Parkinson's Disease
Interventions
DRUG

ND0612 (Levodopa/Carbidopa solution)

The total daily dose of levodopa/carbidopa 720/90 mg. Device: CRONO TWIN pump system.

DRUG

ND0612 (Levodopa/Carbidopa solution) + morning oral IR-LD/CD

The total daily dose levodopa/carbidopa from ND0612 538/67 mg. Morning dose of oral IR-LD/CD 150/15 mg. Device: CRONO TWIN pump system.

Trial Locations (11)

30126

Fondazione Ospedale San Camillo - I.R.C.C.S., Venice

45219

University of Cincinnati, Cincinnati

48334

QUEST Research Institute, Farmington Hills

56126

AOU Pisa, Pisa

56520

Chaim Sheba Medical Center, Ramat Gan

60611

Northwestern University, Chicago

64239

Sourasky Medical Center, Tel Aviv

66100

University Foundation, Chieti

4941492

Rabin Medical Center, Petah Tikva

A- 4060

Medical University Innsbruck, Innsbruck

00163

IRCCS San Raffaele Pisana, Rome

Sponsors

Lead Sponsor

All Listed Sponsors
lead

NeuroDerm Ltd.

INDUSTRY

NCT02577523 - A Clinical Study of Efficacy, Safety, Tolerability and PK of ND0612H in Subjects With Advanced Parkinson's Disease | Biotech Hunter | Biotech Hunter