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Study to Evaluate and Compare Safety and Pharmacokinetics of the HCP1004 and VIMOVO 500/20mg in Healthy Korean Male

Hanmi Pharmaceutical logo

Hanmi Pharmaceutical

Status

Completed

Conditions

Rheumatoid Arthritis

Study type

Observational

Funder types

Industry

Identifiers

NCT01688193
HM-ESNP-102

Details and patient eligibility

About

The purpose of this study is to Evaluate and Compare Safety and Pharmacokinetics of the HCP1004 and VIMOVO 500/20mg in Healthy Korean Male

Enrollment

68 patients

Sex

Male

Ages

20 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • BMI: 18.0 - 27.0 kg/m2
  • Willingness to sign the written Informed Consent Form

Exclusion criteria

  • Evidence of clinically relevant pathology
  • History of relevant drug and food allergies
  • Positive screen on drugs of abuse
  • Participation in a drug study within 60 days prior to drug administration.

Trial design

68 participants in 2 patient groups

HCP 1004
Vimovo 500/20mg

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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