Bioequivalence Study
Conditions
Brief summary
The aim of this study is to evaluate the bioequivalence of two Calcium Hydroxybenzene Dispersible Tablets in healthy Chinese volunteers.
Detailed description
The trial preparation is Calcium Hydroxybenzene Sulphonate Dispersible Tablets produced by Hainan Linheng Pharmaceutical Co., Ltd. The reference preparation is Calcium Hydroxybenzene Sulphonate Tablets (Doxium ®) produced by OM pharma S.A. The bioequivalence of two preparations will be evaluated at the fast or fed conditions.
Interventions
DRUGCalcium Hydroxybenzene Sulphonate Dispersible Tablets 0.25g
A generic product manufactured by Hainan Linheng Pharmaceutical Co., Ltd.
DRUGCalcium Hydroxybenzene Sulfonate Tablets（Doxium®) 250mg
Calcium Hydroxybenzene Sulfonate Tablets（Doxium®）produced by OM pharma S.A.
Sponsors
Hainan Linheng Pharmaceutical Co., Ltd.
Beijing Tongren Hospital
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes
Inclusion criteria
1. Participate voluntarily and sign an informed consent form before the study; 2. Age: 18 to 55 years old (including 18 and 55 years old) , male and female; 3. Weight: female subjects with weight ≥45.0kg, male subjects with weight ≥50.0kg, with the body mass index of 19.0\ 28.0 kg/m (including 19.0 and 28.0); 4. The physical examination, vital signs, laboratory examination and electrocardiogram are not abnormal or abnormal but with no clinical significance; 5. Have no pregnancy plan and appropriate contraceptive measures during the trial and within 6 months after the last dose. 6. Be able to communicate well, understand and comply with the requirements of the study.
Exclusion criteria
1. Be allergic, or have a clear history of allergies to trial drugs and excipients; 2. Have diseases in circulatory system, respiratory system, digestive system, hematologic system, nervous system, immune system, urinary system, endocrine system and mental system, or have medical history of the above-mentioned systems and other diseases that may significantly affect drug absorption, distribution, metabolism and excretion. 3. Have a history of drug abuse or are positive for urine durg screening; 4. Pregnant or lactating women, or serum HCG positive for female subjects, or there was a unprotected sex within 2 weeks before screening; 5. Frequent smokers and alcoholics within the first 3 months (smoking more than 5 cigarettes/day on average, drinking an average of more than 21 units of alcohol per week, 1 unit = 360 mL beer or 45 mL liquor or 150 mL wine), or cannot stop using any tobacco products, or unable to stop alcohol intake during the whole research; 6. Have donated more than 400 mL of blood within 3 months before screening, or lost more than 400 mL of blood for other reasons, or donated plasma within 14 days before screening; 7. Have used any prescription drugs, vaccines, Chinese herbal medicine within 4 weeks before first dose of the research drug, and/or use any over-the-counter drugs (OTC), vitamins, nutritional supplements within 2 weeks before first dose of the research drug; 8. Have participated in any clinical trial within 3 months before screening; 9. Refuse to stop using any methylxanthine drinks or foods such as coffee, tea, cola, chocolate, or drinks containing grapefruit, or any food that affect the activity of liver enzymes from 48 hours before the first dose of the research drug to the end of the study; 10. Have undergone surgery within 6 months before screening, or plan to receive a surgery recently ; 11. Have abnormality or clinical significance in any infection screening; 12. Have special requirements on diet and cannot accept unified diet; 13. Have the difficulty in venous blood taking or can not tolerate venipuncture, or have a history of dizziness in blood taking; 14. Any other condition that researchers believe unsuitable for enrolling into the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Bioequivalence based on Cmax | Pharmacokinetic plasma samples collected over 36 hour period | Cmax - Maximum Observed Concentration in Plasma |
| Bioequivalence based on AUC 0-t | Pharmacokinetic plasma samples collected over 36 hour period | Area Under the Concentration-time Curve From Time Zero to Time of Last |
| Bioequivalence based on AUC 0-∞ | Pharmacokinetic plasma samples collected over 36 hour period | Area Under the Concentration-time Curve From Time Zero to Infinity (Extrapolated) |
Countries
China
Contacts
Primary ContactFeng Wu, Dr
Outcome results
None listed