An Open-label, Randomized, 3-way Crossover Study to Evaluate the Pharmacokinetics of Investigational Product Ibuprofen Modified-Release Tablets 800 mg Compared to Ibuprofen Tablets 800 mg in Healthy Volunteers
Trial Snapshot
- Phase
- Phase 1
- Status
- Completed
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- To evaluate the food effects of IBUMR on PK parameters
Study Overview
Brief Summary
An open-label, randomized, 3-way crossover study to evaluate the pharmacokinetics of investigational product "Ibuprofen Modified-Release Tablets 800 mg" in comparison to the reference standard "Ibuprofen Regular-Release Tablets 600 mg/800 mg" in normal healthy volunteers
Primary objective:
To evaluate the food effect of IBUMR and its bioavailability of single and multiple doses compared with reference drugs in normal healthy volunteers.
Secondary objectives:
- To determine and compare the single and multiple dose PK profiles of IBUMR and reference drugs.
- To identify the effect duration for IBUMR after dose administration by detecting ibuprofen concentrations in plasma.
- To evaluate the safety profile of single and multiple doses of IBUMR.
Detailed Description
This study consists of 3 treatment periods as below. For Treatment A and Treatment B, single- and multiple-dose stages are included.
Treatment A:
One tablet of IBUMR will be administered to the subjects under fasted condition, followed by a minimum of 72-hour washout interval. After the washout period, subjects will receive 1 × IBUMR every 12 hours for a total of 8 doses.
Treatment B:
One tablet of IBURed-800mg will be administered to the subjects under fasted condition, followed by a minimum of 72-hour washout interval. After the washout period, subjects will receive 1 × IBURed-600mg every 8 hours for a total of 12 doses.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Crossover
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Subjects whose body mass index (BMI) at screening is within a range of ≥18.5 kg/m2 and <25.0 kg/m
- •BMI = Body Weight (kg) / [Height (m)]2 And body weight is not less than 50 kg and 45 kg for males and females, respectively.
- •Subject's medical history shows no contraindication to the test medications (hypersensitivity to ibuprofen or any component of test and reference products) and non-steroidal anti-inflammatory drugs (NSAIDs).
- •Subjects who are judged to be in good health by the investigator based upon the results of physical examination (PE), vital signs, and routine laboratory tests.
- •The female subject shows negative pregnancy test results within 30 days prior to the first dose of the study.
- •The subject did not take any of the following medications in the specified durations:
- •Any systemically absorbed medication within 14 days (excluding vitamins, food supplements and hormone contraceptives not ibuprofen drug interactions) prior to the first dose of the study
- •Any enzyme inducer/inhibitor and/or known hepatic or renal clearance-altering agents (e.g., erythromycin, cimetidine, barbiturates, phenothiazine, clarithromycin, troleandomycin, ketoconazole, miconazolem fluconazole, itraconazole) within 30 days prior to the first dose of the study.
- •Subjects are willing to comply with protocol-stated requirements, instructions and restrictions, followed by understanding and signing the written informed consent form by the subject or legal representative if he/she is under the statutory age of consent as per the local authority.
Exclusion Criteria
- •Subjects with any properly diagnosed disease within 30 days prior to the first dose of the study.
- •Subjects with a clinically significant hematological, endocrine, cardiovascular, hepatic, renal, gastrointestinal, and/or pulmonary disorder; subjects with any predisposing condition that might interfere with the absorption, distribution, metabolism and excretion of drugs; subjects who has had any previous gastrointestinal surgery or coronary artery bypass graft.
- •Subjects who require treatment with any medications, either prescription or non-prescription (excluding vitamins and food supplements), within 30 days prior to the first dose of the study
- •Subjects have participated in investigational drug trials and took any investigational drug within 60 days prior to the first does of the study.
- •Subjects had blood donation more than 250 and 500 mL within 60 and 90 days, respectively prior to the first dose of the study.
- •Subjects had a history of drug abuse or alcohol abuse according to the Diagnostic and Statistical Manual of Mental Disorders 4th edition (DSM-IV) criteria.
- •Subjects cannot stop smoking and caffeine-intakes for 48 hours prior to the first dose of the study and during the entire study period.
- •Subjects who are pregnant or lactating.
- •Subjects who have been tested positive for the following tests:
- •Human immunodeficiency virus (HIV)
- •Hepatitis B virus (HBV)
- •Hepatitis C virus (HCV)
- •Treponema pallidum (STS test)
- •For enrollment of female subjects with child-bearing potential, the subject must be practicing sexual abstinence or be using and willing to continue to use a medically acceptable form of birth control for at least 30 days prior to screening (that period will extend to 3 months for oral contraceptive use) and for at least 30 days after the last dose of study drug. For a subject to be considered not to be of child-bearing potential, she must have been amenorrheic for at least 2 years, or must have had a hysterectomy, a bilateral tubal ligation, and/or a bilateral oophorectomy (as determined by the medical history). The male partner of a female study subject with childbearing potential must use a condom and ensure that his partner uses a suitable method of contraception as outlined above.
- •Subjects with underlying medical, mental, psychological, or other inappropriate conditions that would impair treatment compliance, or in the opinion of the investigator would not permit to participate in the study.
Arms & Interventions
Treatment ABC
Receive the investigational product and active comparator in a sequence of treatment A, treatment B and treatment C.
Intervention: Ibuprofen Tablets (Drug)
Treatment ACB
Receive the investigational product and active comparator in a sequence of treatment A, treatment C and treatment B.
Intervention: Ibuprofen Tablets (Drug)
Treatment BAC
Receive the investigational product and active comparator in a sequence of treatment B, treatment A and treatment C.
Intervention: Ibuprofen Tablets (Drug)
Treatment BCA
Receive the investigational product and active comparator in a sequence of treatment B, treatment C and treatment A.
Intervention: Ibuprofen Tablets (Drug)
Treatment CAB
Receive the investigational product and active comparator in a sequence of treatment C, treatment A and treatment B.
Intervention: Ibuprofen Tablets (Drug)
Treatment CBA
Receive the investigational product and active comparator in a sequence of treatment C, treatment B and treatment A.
Intervention: Ibuprofen Tablets (Drug)
Outcomes
Primary Outcomes
To evaluate the food effects of IBUMR on PK parameters
Time Frame: After collecting blood samples from the last participant, up to 30 days
To assess the food effect of IBUMR in the PK parameters including AUCL
Comparison of single-dose and multi-dose bioavailability of IBUMR and IBURed
Time Frame: After collecting blood samples from the last participant, up to 30 days
Comparison of single-dose and multiple-dose bioavailability between IBUMR and IBURed in log-transformed values of the peak concentration (Cmax)
Comparison of single - and multi-dose bioavailability of IBUMR and IBURed
Time Frame: After collecting blood samples from the last participant, up to 30 days
Comparison of single-dose and multiple-dose bioavailability between IBUMR and IBURed in log-transformed values of area under the curve from time 0 to infinity (AUCinf).
To assess the food effect of IBUMR in the PK parameters
Time Frame: After collecting blood samples from the last participant, up to 30 days
To assess the food effect of IBUMR in the PK parameters including Cmax
To evaluate the food effect of IBUMR on PK parameters
Time Frame: After collecting blood samples from the last participant, up to 30 days
To assess the food effect of IBUMR in the PK parameters including time to reach peak concentration (Tmax)
Evaluate the food effect of IBUMR in PK parameters
Time Frame: After collecting blood samples from the last participant, up to 30 days
To assess the food effect of IBUMR in the PK parameters including AUCinf
Comparison of single-dose and multiple-dose bioavailability between IBUMR and IBURed
Time Frame: After collecting blood samples from the last participant, up to 30 days
Comparison of single-dose and multiple-dose bioavailability between IBUMR and IBURed in log-transformed values of area under the curve from time 0 to the last measurable concentration (AUCL)
Determine the food effect of IBUMR in PK parameters
Time Frame: After collecting blood samples from the last participant, up to 30 days
To assess the food effect of IBUMR in the PK parameters including elimination half-life (t1/2)
Secondary Outcomes
- Single dose PK step(After collecting blood samples from the last participant, up to 30 days)
- Single dose PK(After collecting blood samples from the last participant, up to 30 days)
- Incidence of sudden adverse events (safety and tolerability)(After collecting blood samples from the last participant, up to 60 days)
- Single-dose PK measures(After collecting blood samples from the last participant, up to 30 days)
- Single dose PK design(After collecting blood samples from the last participant, up to 30 days)
- Multiple - dosed PK(After collecting blood samples from the last participant, up to 30 days)
- Multiple - dosed PK steps(After collecting blood samples from the last participant, up to 30 days)
- Multiple - dosed PK method(After collecting blood samples from the last participant, up to 30 days)
- Multiple - dosed PK program(After collecting blood samples from the last participant, up to 30 days)
- Evaluation of duration of IBUMR effect(After collecting blood samples from the last participant, up to 30 days)
- Incidence of treatment-emergent adverse events (safety and tolerability)(After collecting blood samples from the last participant, up to 60 days)
- Single dose PK method(After collecting blood samples from the last participant, up to 30 days)
- Multiple-dose PK measures(After collecting blood samples from the last participant, up to 30 days)
- Multiple - dosed PK plan(After collecting blood samples from the last participant, up to 30 days)
- Multiple - dosed PK arrangement(After collecting blood samples from the last participant, up to 30 days)
- Multiple - dosed PK planning(After collecting blood samples from the last participant, up to 30 days)
- Assessment of effect duration for IBUMR(After collecting blood samples from the last participant, up to 30 days)
- safety and tolerability(After collecting blood samples from the last participant, up to 60 days)
- Incidence of treatment-induced adverse events (safety and tolerability)(After collecting blood samples from the last participant, up to 60 days)
- Single dose PK moves(After collecting blood samples from the last participant, up to 30 days)
- Multiple - dosed PK design(After collecting blood samples from the last participant, up to 30 days)
- Multiple - dosed PK process(After collecting blood samples from the last participant, up to 30 days)
- Incidence of treatment-emergent adverse events(After collecting blood samples from the last participant, up to 60 days)