Pharmacokinetic Study of Lansoprazole Capsules in Healthy Chinese Volunteer

Zhejiang University

Status and phase

Completed

Phase 1

Conditions

Effect of Drugs

Safety Issues

Treatments

Drug: Lansoprazole capsules

Study type

Interventional

Funder types

Other

Identifiers

NCT03488173

LC00-018-01

Details and patient eligibility

About

The objective of this study was to compare pharmacokinetic of Lansoprazole Capsules 30 mg with Lansoprazole Capsules of Takeda 30 mg in healthy adult human subjects.

Full description

i. randomized, open label, single-dose, two-treatment, three-period,partial replicate pharmacokinetic study of Lansoprazole 30 mg Capsules of Beijing Sihuan Pharm, comparing with that of Lansoprazole enteric-coated Capsules 30 mg of Takeda Pharmaceutical Company Limited in healthy, adult, human subjects under fasting conditions.

ii. randomized, open label, single dose, two-period, pharmacokinetic study of Lansoprazole 30 mg Capsules of Beijing Sihuan Pharm in healthy, adult, human subjects under fasting/fed conditions.

Enrollment

42 patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Subject who were healthy, adult, human beings within 18 and 60 years of age (both inclusive)
Male (weight ≥50kg) or female (weight ≥45kg); Subject having a body mass index between 19.0 and 26.0 (both inclusive), calculated as weight in Kg/height in m2.
Subject who totally understand the aim, procedure, benefits and adverse effects of this clinical trial, make decision by his/her free will, and sign a consent form to follow the progress;
The participant could communicate well with investigator, comply with and finish the study according to the procedure.

Exclusion criteria

Subject who has past or present history of any serious diseases, including (but not limited to) digestive, cardiovascular, respiratory, urinary, musculoskeletal, endocrine, psychiatric or neurological, hematologic, immunological or metabolic disorders;
Allergy/hypersensitivity (including drug allergy) which is deemed relevant to the trial as judged by the investigator;
Intake of over the counter (OTC) or prescribed medications or vitamins or any traditional medicine products for the last 14 days before first dosing.
Has a special requirement for food and cannot adhere to a uniform diet or swallowing victims.
Venous puncture intolerable and/or blood phobia
Abused of tea, coffee and caffeine-contained beverages; or taking caffeine/xanthene containing food or beverages (like tea, coffee, chocolates and cola drinks) for the last 48 hrs before first dosing.
Habit of alcoholism; or frequent drinkers for the last 6 months before screening; or intake of any alcoholic products for the last 24 hrs before first dosing.
Regular smoker who has a habit of smoking more than five cigarettes per day for the last 3 months and has difficulty in abstaining from smoking during sample collection period.
Blood donation or blood loss ≥ 450 mL for the last 3 months before first dosing; or plan to donate blood or blood composition during the study or 3 months after the end of the study.
Intake of any enzyme modifying food or beverages for the last 48 hrs before first dosing.
Female detected to be pregnant, breast feeding or who is likely to become pregnant during the study; or subjects declined to practice non-pharmacologic prevention of birth control during the study.
Abused of drugs or Intake of drugs for the last 3 months before screening.
Subjects who had participated in any other clinical investigation using experimental drug/medical instrument/diagnostic reagent in past 3 months before screening.
Clinically significant abnormalities judged by investigators during screening test.
Confirmed positive in alcohol screening, smoking screening or selected drug of abuse.
Human immunodeficiency virus(HIV), hepatitis B virus (HBV), hepatitis C virus (HCV) or syphilis positive.
Other reasons for non-inclusion judged by investigator.