Tolerability and Steady-state Pharmacokinetics of BIA 6-512

PHASE1CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

May 11, 2005

Primary Completion Date

July 29, 2005

Study Completion Date

July 29, 2005

Conditions
Parkinson Disease
Interventions
DRUG

BIA 6-512

The investigational products consisted of capsules containing BIA 6-512 25 mg, 50 mg, 100 mg and 150 mg. Products were administered orally, with approximately 240 mL of water in case of Doses 1 and 13, and at least 150 mL of water in case of Doses 2 to 12. First dose (Dose 1) and last dose (Dose 13) were administered in fasting of at least 8 hours and subject remained fasted until to 2.5 h post-dose. Meals were not served within 1 hour prior and 1 hour after investigational product administration in Doses 2 to 12

DRUG

Placebo

Matching placebo capsules

Trial Locations (1)

4745-457

Human Pharmacology Unit (UFH) - BIAL - Portela & Cª, SA, S. Mamede Do Coronado

All Listed Sponsors
lead

Bial - Portela C S.A.

INDUSTRY

NCT03093389 - Tolerability and Steady-state Pharmacokinetics of BIA 6-512 | Biotech Hunter | Biotech Hunter