Long-term Administration Study of SND 919 Tablets in Parkinson's Disease

Boehringer Ingelheim

Status and phase

Completed

Phase 3

Conditions

Parkinson Disease

Treatments

Drug: Pramipexole 0.125 mg tablets

Drug: Pramipexole 0.5 mg tablets

Study type

Interventional

Funder types

Industry

Identifiers

NCT00274131

248.506

Details and patient eligibility

About

To evaluate the efficacy and safety of long-term treatment with pramipexole tablets (BI Sifrol®) in Parkinson's disease (phase III study).

Full description

The efficacy and safety of long-term treatment with pramipexole (BI Sifrol®) were evaluated in Parkinson disease patients in an open-label non-controlled design. The treatment was initiated at 0.125 mg bid (after breakfast and supper).

The dose was increased stepwise with due caution regarding the symptoms and safety of each patient, up to 1.5 mg tid (after each meal). The treatment period was set at 56 weeks, followed by a stepwise dosedecreasing period (maximum 4 weeks).

Study Hypothesis:

Comparison(s):

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients with a diagnosis of Parkinson's disease (including juvenile parkinsonism)

(1) Patients meeting all of the following inclusion criteria

Patients of at least 20 years of age
In- or outpatients of either sex.
Patients in any stage on the modified Hoehn and Yahr severity scale

Exclusion criteria

Patients with psychiatric symptoms such as confusion, hallucination, delusion, excitement, delirium, and abnormal behaviour.
Patients with subjective symptoms derived from orthostatic hypotension.
Patients with hypotension (systolic blood pressure <100 mmHg)
Patients with concomitant illness such as severe cardiac, renal, and hepatic disease
Patients with a current or past history of epilepsy
Pregnant, possibly pregnant, or lactating women
Patients receiving any other investigational products or who have received any other investigational product within 6 months of the study.
Patients who judged incompetent to give consent
Others judged by the investigator or co-investigator to be ineligible as subjects.