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Clinical Pharmacokinetics Study on Pikamilone

C

Chinese Academy of Sciences

Status

Completed

Conditions

Healthy

Study type

Observational

Funder types

Other

Identifiers

NCT00940186
SIMM-DMPK-080901

Details and patient eligibility

About

Study on the phamacokinetics of Pikamilone in healthy Chinese subject and provide informations for further phase II study.

Enrollment

30 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • nonsmokers and in good health
  • weight: BMI: 19-24
  • written informed consent was finished.

Exclusion criteria

  • disease
  • taking any drug, alcohol, foods containing caffeine, or grapefruits and juice before study.

Trial design

30 participants in 3 patient groups

pikamilone
dosage
Description:
low dosage group: administrate pikamilone tablet 50 mg; middle dosage group: administrate pikamilone tablet 100 mg; hige dosage group: administrate pikamilone tablet 200 mg.
tablet

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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