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Completed

NCT Number: NCT01424176

Dexpramipexole Renal PK Study

This is a multicenter, open-label, single-dose, PK and safety study in subjects with various stages of renal impairment.

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Key information

About this study

Dexpramipexole (BIIB050, KNS-760704; (6R)-4,5,6,7-tetrahydro-N6-propyl-2,6-benzothiazolediamine dihydrochloride monohydrate) is a synthetic amino-benzothiazole. Data from multiple in vitro and in vivo assays have suggested that dexpramipexole is neuroprotective. It is being investigated for the treatment ALS.

As dexpramipexole is principally eliminated from the body by the kidneys a single oral dose of dexpramipexole will be administered to subjects with various stages of renal impariment comprising the following categories: mild, moderate, severe and ESRD subjects. Healthy volunteers will be matched to each catergory of renal impaired subjects.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult males/females aged 18 to 75 years inclusive and between 19 and 36 kg/m2 inclusive BMI.
  • Subjects with renal impairment must have stable renal disease (i.e., no change in disease status within the 28 days prior to dosing) as determined by the Investigator with laboratory and clinical findings that support the diagnosis of renal impairment.
  • Subjects with renal impairment (excluding ESRD subjects), must have 2 separate estimates of creatinine clearance that are within 25% of each other, obtained >5 days apart, but not >6 months apart
  • Subjects must have a GFR (estimated GFR; as defined by estimation of creatinine clearance using the MDRD formula) of ≥80 (healthy volunteers), between 50 and 79 (mild renal impairment), between 30 and 49 (moderate renal impairment), or <30 (severe renal impairment), or must require dialysis ≤3 times a week (ESRD).
  • Healthy volunteers must be matched to renally impaired subjects for age (± 10 years), gender, and if possible BMI (± 20%).

Exclusion criteria

  • Healthy volunteers who have received prescription medication within the 14 days prior to dosing (except for birth control).
  • Renally impaired subjects who have received prescription medication within the 14 days prior to dosing (except for birth control and medications taken at a stable dose for underlying conditions, as determined by the Investigator).

Treatment and study plan

Dexpramipexole (dose 1)

Drug

Other names: BIIB050

Dexpramipexole (dose 2)

Drug

Other names: BIIB050

Primary outcomes

  1. AUC after single dose of dexpramipexole

    Time frame: pre dose and at 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 16, 24, 36, 48, and 72 hours after dosing in all subjects, and in addition at 96, 120, and 144 hours after dosing in subjects with severe renal impairment and ESRD.

  2. Cmax after single dose of dexpramipexole

    Time frame: pre dose and at 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 16, 24, 36, 48, and 72 hours after dosing in all subjects, and in addition at 96, 120, and 144 hours after dosing in subjects with severe renal impairment and ESRD.

Secondary outcomes

  1. Mointoring of Clinical Laboratory tests

    Time frame: pre-144 hours post dose

  2. ECG Monitoring

    Time frame: pre-144 hrs post dose

  3. Vital Sign monitoring

    Time frame: pre-144 hrs post dose

  4. AE monitoring

    Time frame: pre-144 hrs post dose

Sponsors and collaborators

Lead sponsor

Knopp Biosciences

Industry

Registry information

Official study title

A Multicenter, Open-Label, Single-dose, Pharmacokinetic and Safety Study of Dexpramipexole (BIIB050) in Healthy Subjects and Subjects With Renal Impairment

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
Aug 26, 2011
Registry last updated
Nov 25, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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