Skip to content

A randomized, open, two-cycle, self-crossover design to evaluate the bioavailability of a single oral amlodipine besylate tablet and the original amlodipine besylate tablet in Chinese healthy subjects under fasting and postprandial conditions Degree and bioequivalence studies

A randomized, open, two-cycle, self-crossover design to evaluate the bioavailability of a single oral amlodipine besylate tablet and the original amlodipine besylate tablet in Chinese healthy subjects under fasting and postprandial conditions Degree and bioequivalence studies

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015238
Enrollment
Unknown
Registered
2018-03-16
Start date
2018-03-01
Completion date
Unknown
Last updated
2018-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular diseases

Interventions

fast:5mg every set
fed:5mg every set

Sponsors

The First Affiliated Hospital, ZheJiang Univercity
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Aged 18-45 years old male and female; 2) Male subjects weighing 50kg or more (including 50kg), female subjects weighing more than 45kg (including 45kg); body mass index [BMI=weight (kg)/height (m)2] within the range of 19-28kg/m2 Inside; 3) According to previous medical history, comprehensive physical examination and prescribed laboratory tests, the investigator determined that they were healthy subjects; 4) Women of childbearing age had a negative blood pregnancy test and were taken from 14 days prior to dosing to 6 months after the end of the study. Effective contraceptive measures; 5) Male volunteers must take effective contraceptive measures 14 days before dosing and up to 6 months after the end of the study and agree to not perform sperm donation within six months from the end of the study; 6) Fully understand the purpose of the trial, the nature of the trial, the study procedures, and possible adverse reactions, and voluntarily participate in the trial and sign an informed consent form (the process of obtaining informed consent meets GCP requirements); 7) Communicate well with the researcher, follow the requirements of the entire study, and be willing to stay in the Phase I clinical research ward as required.

Exclusion criteria

Exclusion criteria: 1. Can not tolerate venipuncture blood collection; 2. Clearly have a history of allergies to the drug components or similar species, or a history of hypersensitivity to two or more other drugs and highly sensitive to food and environmental substances; 3. Have any history of serious clinical illness, including but not limited to digestive system, cardiovascular system, respiratory system, urinary system, musculoskeletal system, endocrine system, neuropsychiatric system, blood system, amlodipine besylate tablets, human organisms, etc. Effectiveness of Shanghai DiSino Biopharmaceutical Co., Ltd. Immune system diseases and metabolic abnormalities; 4. Laboratory tests (blood routine, urine routine, blood biochemistry, etc.) and chest radiographs and electrocardiograms have clinically significant findings within 2 weeks before the test; 5. Hematological screening (HIV antibody or HBV surface antigen or HCV antibody or TP antibody) positive; 6. Women who are breastfeeding, pregnant or planning to become pregnant recently; 7. Positive pregnancy test; 8. Male and female subjects have not taken effective contraception or their spouse plans to have children within six months; 9. Persons with mental or legal disabilities; 10. Screening for history of prescription drug abuse and/or history of illegal drug abuse within the first 6 months of screening; 11. A person who has a history of alcohol abuse within the first 6 months of screening, drinking more than 14 units of alcohol per week (1 unit = 12 ounces or 360 mL beer, 1.5 ounces or 45 mL of 40% alcohol, 5 oz or 150mL wine); 12. Smokers who smoke more than 5 cigarettes per day within the first 6 months of screening; 13. Those who are positive for drug abuse testing or alcohol testing; 14. Persons with history of hospitalization or surgery within 3 months prior to screening (except for appendicitis); 15. Participate in other drug clinical trials within 3 months before screening; 16. Blood donation or acute blood loss (400 mL) within the first 2 months of screening or intended donors within 1 month after the end of the trial; 17. Any other drug used within 2 weeks before the test; 18. Drink more than 1L of tea, coffee, and/or caffeinated beverages daily; 19. Those who do not understand the content of the informed consent and others who do not meet the criteria for the trial enrollment; 20. Researchers consider it inappropriate to participate in the trial (eg, frailty, etc.).

Design outcomes

Primary

MeasureTime frame
Cmax;AUC0-t;

Countries

China

Contacts

Public ContactLiu Jian
lindaliu87@zju.edu.cn+86 0571-87236560

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026