Healthy Volunteers
Conditions
Keywords
PK, GC2129A
Brief summary
The purpose of this study is to evaluate the safety and pharmacokinetics of oral administration of GC2129A in fed conditions to healthy adult volunteers.
Detailed description
This study is an open-label, randomized, fasting, single-dose, 2-group, 2-period, crossover design to evaluate pharmacokinetics that are not affected by blinding. According to the order of administering the investigational drug for each period, 17 people are assigned to each of the two groups and administered. For healthy subjects, each 17 subjects are assigned to each of the two groups(total 34 subjects). If the subject administrate GC2129A in the first period, the subject will be administrated reference drugs in the second period after washout(over 7 days). Conversely, if the subject administrate reference drugs in the first period, the subject will be administrated with GC2129A in the second period.
Interventions
Linagliptin and Metformin Hydrochloride Tablet
Linagliptin 5mg/tab and Metformin Hydrochloride 1000mg/tab (2 tablets)
Linagliptin and Metformin Hydrochloride Tablet
Linagliptin 5mg/tab and Metformin Hydrochloride 1000mg/tab (2 tablets)
Sponsors
GC Biopharma Corp
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
An open-label, randomized, fed, single-dose, 2-group, 2-period, crossover design
Eligibility
Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* A person who is 19 years of age or older at the time of a screening visit * A person with a body mass index (BMI) of 18.0 kg/m2 or more and 30.0 kg/m2 or less with a weight of 50 kg or more (45 kg or more for women) during a screening visit * A person who has no clinically significant congenital or chronic disease during a screening visit and has no pathological symptoms or findings as a result of internal examination
Exclusion criteria
* Persons with clinically significant diseases or history of the digestive system, cardiovascular system, endocrine system, respiratory system, blood and tumor, infectious disease, kidney and urinary reproductive system, mental and nervous system, musculoskeletal system, immune system, otolaryngology, skin system, and ophthalmology. * A person who has a history of gastrointestinal surgery * Those who have taken drug metabolism enzymes, such as barbiturate drugs, within one month of the first dose date or who have taken drugs that may interfere with this clinical trial within 10 days of the first dose date * A person who participates in another clinical trial or biological equivalence test within six months of the first administration date * A person who has donated whole blood within 8 weeks of the date of first administration, or has donated components within 2 weeks, or has received a blood transfusion within 4 weeks * A person who is deemed unsuitable for participation in this clinical trial by the principle investigator(or the delegated sub-investigator) for reasons other than the above selection and
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pharmacokinetic (PK) parameters - Cmax | 0-48hours | Pharmacokinetic (PK) parameters of Metformin in serum |
| Pharmacokinetic (PK) parameters - AUCt | 0-48hours | Pharmacokinetic (PK) parameters of Metformin in serum |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Pharmacokinetic (PK) parameters - AUCinf | 0-48hours | Pharmacokinetic (PK) parameters of Metformin in serum |
| Pharmacokinetic (PK) parameters - Tmax | 0-48hours | Pharmacokinetic (PK) parameters of Metformin in serum |
| Pharmacokinetic (PK) parameters - t1/2 | 0-48hours | Pharmacokinetic (PK) parameters of Metformin in serum |
Countries
South Korea
Contacts
Primary ContactGC Biopharma Corp.
Backup ContactGC Biopharma Corp.
Outcome results
None listed