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Clinical Trials/IRCT20130626013776N7
IRCT20130626013776N7
Completed
未知

Study of the Pharmacokinetic and Pharmacodynamic and Safety Properties of Tinagrast® (300 µg/0.5 ml Syringes, AryaTinaGene Biopharmaceutical Co) in Comparison to Neupogen® (300 µg/0.5 ml syringes, Amgen) in Healthy Volunteers

AryaTinaGene Biopharmaceutical Co0 sites24 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Healthy volunteers.
Sponsor
AryaTinaGene Biopharmaceutical Co
Enrollment
24
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Interventional
Sex
Male

Investigators

Sponsor
AryaTinaGene Biopharmaceutical Co

Eligibility Criteria

Inclusion Criteria

  • Males, 18\-50 years of age.
  • The subject is able and willing to provide written informed consent.
  • The subject is available for the entire study period and is willing to adhere to protocol requirements as evidenced by written informed consent.
  • The subject has stable residence and telephone.
  • Good health as determined by lack of clinically significant abnormalities in health assessments performed at screening.

Exclusion Criteria

  • History of allergy or sensitivity to filgrastim.
  • history of any drug hypersensitivity or intolerance which, in the opinion of the investigator,would compromise the safety of the subject of the study.
  • Significant history or current evidence of chronic infectious disease, system disorder or organ dysfunction.
  • Presence of gastrointestinal disease or history of malabsorption within the last year.
  • History of a medical disorders occurring within the last year that required hospitalization or medication
  • Use of pharmacologic agents known to significantly induce or inhibit drug\-metabolizing enzymes within 30 days prior to dosing.
  • Receipt of any drug as part of a research study within 30 days prior to dosing.
  • Donation or significant loss of whole blood (480 ml or more) within 30 days prior to dosing.

Outcomes

Primary Outcomes

Not specified

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