| Eligibility |
Inclusion Criteria:
- Healthy Thai male or female subjects between the ages of 18 to 55 years
- Body mass index between 18.0 to 30.0 kg/m2.
- Normal laboratory values, including vital signs and physical examination, for all
parameters in clinical laboratory tests at screening. Any abnormalities from the
normal or reference range will be carefully considered clinically relevant by the
physician as individual cases, documented in study files prior to enrolling the
subject in this study
- Non-pregnant woman (negative pregnancy test) and not currently breast feeding
- Female subjects abstain from either hormonal methods of contraception (including oral
or transdermal contraceptives, injectable progesterone, progestin subdermal implants,
progesterone-releasing IUDs, postcoital contraceptive methods) or hormone replacement
therapy for at least 28 days prior to check-in in Period 1. Injectable contraceptives
e.g. Depo-Provera® will be discontinued at least 6 months prior to check-in in Period
1. Subjects agree to use acceptable non-hormonal contraceptive methods such as condom,
diaphragm, foams, jellies or abstinence for at least 14 days prior to check-in in
Period 1 until 7 days after the end of study in Period 2. Female subjects of
non-childbearing potential must meet at least one of the following criteria prior to
check-in in Period 1:
- Postmenopausal for at least 1 year or
- Surgic ally sterile (bilateral tubal ligation, bilateral oophorectomy or hysterectomy)
at least 6 months
- Male subjects who are willing or able to use effective contraceptive e.g. condom or
abstinence after check-in in Period 1 until 7 days after the end of study in Period 2.
- Have voluntarily given written informed consent (signed and dated) by the subject
prior to participating in this study.
Exclusion Criteria:
- History of allergic reaction or hypersensitivity to celecoxib, sulfonamide,
acetylsalicylic acid (aspirin), other NSAIDs including other cyclooxygenase-2 specific
inhibitors or any other ingredient of the product
- History or evidence of clinically significant renal, hepatic, gastrointestinal,
hematological (e.g. anemia), endocrine (e.g. hyper-/hypothyroid, diabetes), pulmonary
or respiratory (e.g. asthma), cardiovascular (e.g. hyper-/hypotension), psychiatric
(e.g. depression), neurologic (e.g. convulsant), allergic disease (including drug
allergies, but excluding untreated, asymptomatic, seasonal allergies at time of
dosing) or any significant ongoing chronic medical illness
- Have high risk for coronavirus infection based on risk assessment questionnaire or
diagnosed as confirmed case of COVID-19
- History about administration of first dose or second dose of COVID-19 vaccine within
30 days prior to check-in in each Period.
- History or evidence of cerebrovascular disease, myocardial infraction, congestive
heart failure, coronary heart disease (stenosed or occluded) or paresis due to
cerebrovascular accident
- History or evidence of cardiovascular bleeding, gastrointestinal bleeding, gastric or
duodenal or peptic ulcer
- History or evidence of galactose intolerance, the Lapp lactase deficiency or
glucosegalactose malabsorption
- History of sensitivity to heparin or heparin-induced thrombocytopenia
- History of problems with swallowing tablet or capsule
- Any condition possibly affecting drug absorption e.g. gastrectomy, enterectomy,
gastritis or duodenal or gastric ulceration other than appendectomy
- History of diarrhea, vomiting or dehydration within 24 hours prior to check-in in each
period
- History or evidence of drug addict or investigation with urine sample shows a positive
test for drug of abuse (morphine, marijuana or methamphetamine)
- 12-lead ECG demonstrating QTc >450 msec, a QRS interval >120 msec or with an
abnormality considered clinically significant at screening. If QTc exceeds 450 msec,
or QRS exceeds 120 msec, the ECG will be repeated two more times and the average of
the three QTc or QRS values will be used to determine the subject's eligibility.
- Investigation with blood sample shows positive test for HBsAg
- Abnormal liver function, = 1.5 times of upper normal limit of reference range for ALT,
AST or bilirubin levels at screening laboratory test
- Have sitting systolic blood pressure of less than 90 mmHg or more than 139 mmHg and
diastolic blood pressure of less than 60 mmHg or more than 89 mmHg on screening or
check-in day. If abnormal blood pressure detects, the measurement will be repeated two
more times after take a rest for at least 5 minutes each. The last measurement value
will be used to determine the subject's eligibility
- History or evidence of habitual use of tobacco or nicotine containing products and
cannot abstain for at least 48 hours prior to check-in in Period 1 and continued for
entire duration of the study
- History or evidence of alcoholism or harmful use of alcohol (less than 2 years) i.e.,
alcohol consumption of more than 14 standard drinks per week for men and 7 standard
drinks per week for women (A standard drink is defined as 360 mL of beer or 150 mL of
wine or 45 mL of 40% distilled spirits, such as rum, whisky, brandy etc.)
- History or evidence of alcohol consumption or alcohol-containing products and cannot
abstain for at least 48 hours prior to check-in in Period 1 and continued for entire
duration of the study or alcohol breath test shows positive result In case of alcohol
breath test result represents the alcohol concentration range of 1 - 10 mg% BAC and
the physician carefully considers that the value came from other reasons, not from the
alcohol drinking behavior of subjects, the test will be repeated two times separately,
not more than 10 minutes. The result of the last time should be used for subject's
eligibility which must be 0 mg%BAC.
- History or evidence of habitual consume of tea, coffee, xanthine or caffeine
containing products and cannot abstain for at least 48 hours prior to check-in in
Period 1 and continued for entire duration of the study
- Consume or drink juice of grapefruit or orange or pomelo or its supplement/containing
products and cannot abstain for at least 7 days prior to check-in in Period 1 and
continued for entire duration of the study
- Use of prescription or nonprescription drugs (e.g. paracetamol, aspirin, antacid,
ketoconazole, erythromycin), herbal medications or supplements (e.g. St. John's wort),
vitamins or mineral (e.g. iron) or dietary supplements within 14 days prior to
check-in in Period 1 and continued for entire duration of the study
- Participated in other clinical trials within 90 days prior to check-in in Period 1
(except for the subjects who drop out or withdrawn from the previous study prior to
Period 1 dosing) or still participates in the clinical trial or participates in other
clinical trials during enrollment in this study
- Blood donation or blood loss = 1 unit (1 unit is equal to 350-450 mL of blood) within
90 days prior to check-in in Period 1 or during enrollment
- Subjects with poor venous access or intolerant to venipuncture
- Unwilling or unable to comply with schedule visit, treatment plan and other study
procedures until end of study
- Inability to communicate well (i.e. language problem, poor mental development,
psychiatric illness or poor cerebral function) that may impair the ability to provide
written informed consent or cooperate with clinical team
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