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Clinical Trials/IRCT20180620040164N17
IRCT20180620040164N17Not yet recruiting未知

Comparative bioequivalence study of Metformin 1000 mg F.C. Tablet of Pharma Chemie and Actoverco. in 24 healthy male under fasting

Pharma Chemie Pharmaceutical Co.0 sites26 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
未知
Status
Not yet recruiting
Sponsor
Enrollment
26

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
20 years to 45 years (—)
Sex
Male

Inclusion Criteria

  • Healthy subjects (male) between 20 – 45 years of age and Body Mass Index (BMI) within 15% of normal range according to the accepted normal values between 18.5 and 30 (inclusive), calculated as kg/m2.
  • Subjects with no significant diseases or clinically significant abnormal findings during screening, medical history, clinical examination and laboratory evaluations.
  • Subjects with normal vital signs.
  • Subjects who agree with patient consent form.

Exclusion Criteria

  • History of allergy or intolerance to metformin or other similar acting agents.
  • Any significant acute or chronic medical illness especially renal insufficiency (Estimated creatinine clearance (Clcr) of < 80ml/min using the Cockcroft Gault formula).
  • Current or recent (within 3 months) gastrointestinal disease.
  • Any major surgery within 4 weeks of study drug administration.
  • Smoking more than 10 cigarettes per day and could not tolerate cigarette cessation during each clinical period.
  • Subjects who has used any drug including prescription or Over-The-Counter (OTC) drugs within 7 days prior to the start of the study and might need drug intake during study period;
  • History of alcohol or drug abuse within 2 years before the start of the study.
  • Heavy drinker of caffeine, grapefruit juice or caffeinated drinks or who are on special diet (such as vegetarians) or do exertional physical activity.
  • A history of difficulty with donating blood or donation of more than 500 ml blood within 7 days prior to the start of the study.

Investigators

Sponsor
Pharma Chemie Pharmaceutical Co.

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