Dexpramipexole Japanese PK Study

Knopp Biosciences

Status and phase: Completed; Phase 1

Conditions: Amyotrophic Lateral Sclerosis

Treatments: Drug: Single dose standard; Drug: Single dose reduced; Drug: Multiple Dose

Study type: Interventional

Funder types: Industry

Identifiers

NCT01424163

223HV101

Details and patient eligibility

About

This is a single and multiple dose, open-label study to evaluate the pharmacokinetics (PK), safety, and tolerability of dexpramipexole administered orally to adult Japanese and Caucasian healthy subjects.

Full description

The study is designed to evaluate the influence of ethnic factors on dexpramipexole safety, tolerability, and PK. Subjects will be admitted to the clinical unit on Day -1 (the day prior to first dosing) and will remain in the clinical unit under observation until discharge. All subjects will have a final follow up visit. Whilst resident in the clinic, subjects will receive 4 treatments: The first 3 treatments comprise Part A of the study and the final treatment group comprises Part B.

Part A:

Treatment 1: Dose 1 (reduced) of dexpramipexole; a single dose Treatment 2: Dose 2 (standard) dexpramipexole; a single dose Treatment 3: Dose 3 (standard) dexpramipexole; 5 doses administered at 12 hour intervals Part B: Dose 4 (standard) dexpramipexole; 5 doses administered at 12 hour intervals There will be a minimum washout of 3 days between treatments.

For all subjects, prior to proceeding to the next treatment group, safety and tolerability data will be reviewed.

Caucasian subjects will be matched individually (on a 1:1 basis) to Japanese subjects with respect to gender and age and if possible BMI.

Enrollment: 57 patients

Sex: All

Ages: 18 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Subjects who are able and willing to give written informed consent.
• Adult Japanese and Caucasian males/females aged 18 to 60 years inclusive and between 18 and 30 kg/m2 body mass index (BMI), inclusive.
• Male and female subjects will be enrolled on the study. Male subjects and female subjects of childbearing potential, must practice effective contraception during the study and be willing and able to continue contraception for 1 month (females) or 3 months (males) after their last dose of study treatment
• Japanese subjects must be born in Japan and have both parents and four grandparents of Japanese descent.
• Japanese subjects must have lived outside of Japan for no more than 5 years.
• Japanese subjects must not have significant changes with regard to diet; i.e., their diet must not have significantly changed since leaving Japan.
• Caucasian subjects will be matched individually (on a 1:1 basis) to Japanese subjects with respect to gender and age, and if possible BMI.

Exclusion criteria

• Subjects who do not conform to the above inclusion criteria.
• Female subjects who are pregnant, trying to become pregnant or lactating.
• Subjects who have a clinically relevant history or presence of respiratory, gastrointestinal, renal, hepatic, hematological, lymphatic, neurological, cardiovascular, psychiatric, musculoskeletal, genitourinary, immunological, dermatological, connective tissue diseases or disorders.
• Subjects who have a clinically relevant surgical history.
• Subjects who have previously received dexpramipexole or pramipexole.

Trial design

Primary purpose: Basic Science

Allocation: Non-Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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57 participants in 4 patient groups

Treatment 1 (Part A)

Experimental group

Description:

Dexpramipexole single dose (reduced dose)

Treatment:

Drug: Single dose reduced

Treatment 2 (Part A)

Experimental group

Description:

Dexpramipexole single dose (Standard dose)

Treatment:

Drug: Single dose standard

Treatment 3 (Part A)

Experimental group

Description:

Dexpramipexole multiple dosing

Treatment:

Drug: Multiple Dose

Drug: Multiple Dose

Treatment for Part B

Experimental group

Description:

Dexpramipexole multiple dosing

Treatment:

Drug: Multiple Dose

Drug: Multiple Dose