ClinicalTrials.gov record
Completed Phase 2Phase 3 Interventional Results available

Safety, Tolerability and Efficacy of Two Doses of Once Daily P2B001 in Subjects With Early Parkinson's Disease

ClinicalTrials.gov ID: NCT01968460

Public ClinicalTrials.gov record NCT01968460. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 11, 2026, 9:05 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2B, Twelve-week Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study, To Determine the Safety, Tolerability and Efficacy of Two Doses of Once Daily P2B001 in Subjects With Early Parkinson's Disease

Study identification

NCT ID
NCT01968460
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Pharma Two B Ltd.
Industry
Enrollment
149 participants

Conditions and interventions

Interventions

  • P2B001 once daily (pramipexole 0.3 mg / rasagiline 0.75 mg), Drug
  • P2B001 once daily (pramipexole 0.6 mg / rasagiline 0.75 mg), Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
35 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2013
Primary completion
Apr 30, 2015
Completion
May 31, 2015
Last update posted
Apr 6, 2023

2013 – 2015

United States locations

U.S. sites
24
U.S. states
18
U.S. cities
24
Facility City State ZIP Site status
P2B001 Site Birmingham Birmingham Alabama
P2B001 Site Los Angeles Los Angeles California
P2B001 Site Aurora Aurora Colorado
P2B001 Manchester Manchester Connecticut
P2B001 Site New Haven New Haven Connecticut
P2B001 Site Boca Raton Boca Raton Florida
P2B001 Site Port Charlotte Port Charlotte Florida
P2B001 Site Tampa Tampa Florida
P2B001 Site Augusta Augusta Georgia
P2B001 site Chicago Chicago Illinois 60612
P2B001 Site Kansas City Kansas City Kansas
P2B001 Site Boston Boston Massachusetts
P2B001 Site west Bloomfield West Bloomfield Michigan
P2B001 Site Golden Valley Golden Valley Minnesota
P2B001 Site Camden Camden New Jersey
P2B001 Site New Brunswick New Brunswick New Jersey
P2B001 site Commack Commack New York
P2B001 Site New York New York New York
P2B001 Site Durham Durham North Carolina
P2B001 Site Cincinnati Cincinnati Ohio
P2B001 Site Toledo Toledo Ohio
P2B001 Site Tulsa Tulsa Oklahoma
P2B001 Site Houston Houston Texas
P2B001 Site Roanoke Roanoke Virginia

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01968460, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 6, 2023 · Synced May 11, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01968460 live on ClinicalTrials.gov.

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