Safety and Pharmacokinetics of UI112 Compared With UIC202611 in Healthy Adults
A Randomized, Open-Label, Single-Dose, 2x2 Crossover Clinical Trial to Compare and Evaluate the Safety and Pharmacokinetics After Subcutaneous Administration of UI112 or UIC202611 in Healthy Adult Subjects
This Phase 1 clinical trial aims to compare the pharmacokinetics and safety of UI112 and UIC202611 (Wegovy), two injectable products containing semaglutide, in healthy adult volunteers.
A total of 44 healthy adults will be randomly assigned to one of two treatment sequences. Each participant will receive a single 0.5 mg subcutaneous injection of UI112 and UIC202611 in separate treatment periods, with a 6-week washout period between administrations.
Blood samples will be collected at scheduled time points to measure semaglutide concentrations and compare how the two products are absorbed and eliminated from the body. Safety will also be assessed through adverse events, physical examinations, vital signs, electrocardiograms, and laboratory tests.
Tutkimuksen yleiskatsaus
Tila
Tila
Ehdot
Ehdot
Interventio / Hoito
Interventio / Hoito
Yksityiskohtainen kuvaus
This is a randomized, open-label, single-dose, two-period, two-sequence crossover Phase 1 clinical trial conducted in healthy adult volunteers.
Participants will be randomly assigned to one of two treatment sequences:
- Sequence A: UIC202611 in Period 1, followed by UI112 in Period 2.
- Sequence B: UI112 in Period 1, followed by UIC202611 in Period 2.
Each participant will receive a single 0.5 mg dose of semaglutide by subcutaneous injection into the abdomen during each treatment period. A 6-week washout period will separate the two administrations.
Blood samples for pharmacokinetic analysis will be collected before dosing and at scheduled intervals up to 504 hours (Day 22) after each administration. The primary pharmacokinetic endpoints are AUCt and Cmax. Secondary pharmacokinetic endpoints include AUC168h, AUCinf, CL/F, Vz/F, Tmax, and t1/2.
Pharmacokinetic equivalence will be evaluated using the geometric mean ratios of AUCt and Cmax between the test and reference products and their corresponding 90% confidence intervals, with predefined equivalence limits of 80.00% to 125.00%.
Safety assessments will include adverse events, physical examinations, vital signs, 12-lead electrocardiograms, clinical laboratory tests, and blood glucose measurements. A post-study visit will be conducted between Day 43 and Day 47 after the final administration.
Opintotyyppi
Opintotyyppi
Ilmoittautuminen (Arvioitu)
Ilmoittautuminen
Vaihe
Vaihe
- Vaihe 1
Yhteystiedot ja paikat
Opiskeluyhteys
Opiskeluyhteys
- Nimi: Min Kyu Park, MD, PhD
- Puhelinnumero: +82-43-269-8708
- Sähköposti: mk_park@cbnuhctc.com
Opiskelupaikat
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North Chungcheong
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Cheongju-si, North Chungcheong, Etelä -Korea, 28644
- Chungbuk National University Hospital
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Ottaa yhteyttä:
- Chungbuk National University Hospital Clinical Trial Center
- Puhelinnumero: +82-43-269-7284
- Sähköposti: cbnuhctc2@naver.com
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Osallistumiskriteerit
Kelpoisuusvaatimukset
Kelpoisuusvaatimukset
Opintokelpoiset iät
Hyväksyy terveitä vapaaehtoisia
Sukupuolet, jotka voivat opiskella
Kuvaus
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Inclusion Criteria:
- Healthy adult volunteers aged 19 years or older and younger than 65 years at screening.
- Participants with a body weight of 50.0 kg to 100.0 kg (inclusive) and a body mass index (BMI) of 20.0 kg/m² to 29.9 kg/m² (inclusive) at screening.
- Participants without congenital diseases or chronic diseases requiring treatment and without pathological symptoms or findings based on a medical examination.
- Participants determined to be suitable for participation in the clinical trial based on clinical laboratory tests, vital signs, physical examinations, and 12-lead electrocardiograms (ECGs) performed at screening.
- Participants who voluntarily decide to participate after receiving and fully understanding detailed information about the clinical trial, provide written informed consent, and agree to comply with the study requirements throughout the clinical trial.
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Exclusion Criteria:
- Current or past history of clinically significant hepatic, renal, neurological, psychiatric, respiratory, endocrine, hematological, neoplastic, genitourinary, cardiovascular, gastrointestinal, musculoskeletal, or other clinically significant diseases.
- Pregnant women (positive urine human chorionic gonadotropin [HCG] test) or breastfeeding women.
- History of hypersensitivity reactions, including anaphylaxis or angioedema, or other clinically significant hypersensitivity to the active ingredient, excipients of the investigational products, or other drugs, including GLP-1 receptor agonists.
- History of skin diseases (e.g., burns or skin cancer) or skin transplantation that may affect the absorption of the investigational products.
- History of acute or chronic pancreatitis.
- Personal or family history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia type 2 (MEN2).
- Clinically significant abnormalities on a 12-lead ECG at screening, including any of the following:
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QTc interval >450 ms in males or >460 ms in females.
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PR interval >200 ms.
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QRS duration >120 ms. 8. Clinically significant abnormalities in clinical laboratory tests at screening, including any of the following:
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AST, ALT, ALP, gamma-GT, or total bilirubin >2 times the upper limit of normal (ULN).
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Serum creatinine outside the reference range or estimated glomerular filtration rate (eGFR), calculated using the CKD-EPI equation, <60 mL/min/1.73 m².
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Lipase or amylase >2 times the ULN.
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HbA1c ≥6.5%. 9. History of drug abuse or a positive urine drug screening test for drugs of abuse.
10. Abnormal vital signs measured in a sitting position after at least 3 minutes of rest at screening, including any of the following:
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Systolic blood pressure ≤90 mmHg or ≥150 mmHg.
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Diastolic blood pressure ≤60 mmHg or ≥100 mmHg.
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Pulse rate ≤40 bpm or ≥100 bpm. 11. Use of drugs that induce or inhibit drug-metabolizing enzymes, such as barbiturates, within 1 month before the first administration of the investigational product.
12. Use of any prescription medication or herbal medicine that may affect the characteristics of the investigational products within 2 weeks before the first administration, or use of any over-the-counter medication or health functional food within 10 days before the first administration. However, participation may be permitted at the investigator's discretion if the medication is not expected to affect the pharmacokinetic characteristics of the investigational products.
13. Participation in another clinical trial involving administration of an investigational product within 6 months before the first administration in this study. The day following the last administration in the previous clinical trial is considered Day 1.
14. Donation of whole blood within 2 months, donation of blood components within 1 month, or receipt of a blood transfusion within 1 month before the first administration, or inability to refrain from blood donation from the time of written informed consent until the post-study visit (PSV).
15. Regular alcohol consumption exceeding 21 units per week within 6 months before the first administration (1 unit = 10 g or 12.5 mL of pure alcohol), or inability to abstain from alcohol from the time of written informed consent until the PSV.
16. Smoking more than an average of 10 cigarettes per day within 3 months before the first administration, or inability to abstain from smoking from 24 hours before the first administration until the final blood sampling.
17. Consumption of grapefruit or grapefruit-containing foods within 72 hours before the first administration, or inability to abstain from such foods until the PSV.
18. Consumption of caffeine-containing foods or beverages (e.g., coffee, green tea, black tea, carbonated beverages, coffee-flavored milk, or energy drinks) within 24 hours before the first administration, or inability to abstain from such products until the final blood sampling.
19. Engagement in strenuous exercise exceeding the level of normal daily activities within 72 hours before the first administration, or inability to refrain from such exercise until the PSV.
20. Inability to maintain dietary habits and physical activity levels comparable to normal daily life from the time of written informed consent until the PSV.
21. Following an abnormal diet that may affect the absorption, distribution, metabolism, or excretion of the investigational products, or consuming foods that may affect drug metabolism.
22. Change in body weight of 5% or more within the previous 3 months. 23. Participants who, or whose spouse or partner, plan to become pregnant, or who do not use reliable contraception even without pregnancy plans, from the time of written informed consent until 60 days after the final administration of the investigational product. Reliable contraceptive methods include implants or intrauterine devices, sterilization procedures (e.g., vasectomy or tubal ligation), and barrier methods (e.g., condoms, contraceptive diaphragms, vaginal sponges, or cervical caps used in combination).
24. Presence of tattoos, sunburn, thermal burns, or other skin abnormalities at the administration site, including cuts, bruising, erythema, induration, or tenderness, that may interfere with medical assessments before or after administration of the investigational products.
25. Participants considered unsuitable for participation in the clinical trial by the investigator for any reason other than the inclusion and exclusion criteria specified above.
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Muut
- Jako: Satunnaistettu
- Inventiomalli: Crossover-tehtävä
- Naamiointi: Ei mitään (avoin tarra)
Aseiden lukumäärä
Aseet ja interventiot
Osallistujaryhmä / ArmOsallistujaryhmä / Arm |
Interventio / HoitoInterventio / Hoito |
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Kokeellinen: Sequence A
Participants will receive a single 0.5 mg subcutaneous dose of UIC202611 (reference product) in Period 1, followed by a single 0.5 mg subcutaneous dose of UI112 (test product) in Period 2, with a 6-week washout period between treatments. |
UI112 is the investigational semaglutide product developed by Korea United Pharm. Co., Ltd. A single 0.5 mg dose will be administered subcutaneously in each participant's assigned treatment period.
Muut nimet:
UIC202611 is the reference product, Wegovy (semaglutide), manufactured by Novo Nordisk. A single 0.5 mg dose will be administered subcutaneously in each participant's assigned treatment period.
Muut nimet:
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Kokeellinen: Sequence B
Participants will receive a single 0.5 mg subcutaneous dose of UI112 (test product) in Period 1, followed by a single 0.5 mg subcutaneous dose of UIC202611 (reference product) in Period 2, with a 6-week washout period between treatments. |
UI112 is the investigational semaglutide product developed by Korea United Pharm. Co., Ltd. A single 0.5 mg dose will be administered subcutaneously in each participant's assigned treatment period.
Muut nimet:
UIC202611 is the reference product, Wegovy (semaglutide), manufactured by Novo Nordisk. A single 0.5 mg dose will be administered subcutaneously in each participant's assigned treatment period.
Muut nimet:
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Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Area Under the Plasma Concentration-Time Curve From Time Zero to the Last Quantifiable Concentration (AUCt) of Semaglutide
Aikaikkuna: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
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AUCt is the area under the plasma concentration-time curve from time zero to the last quantifiable concentration of semaglutide, calculated using the linear trapezoidal method. |
Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
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Maximum Observed Plasma Concentration (Cmax) of Semaglutide
Aikaikkuna: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
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Cmax is the maximum observed plasma concentration of semaglutide following a single subcutaneous administration of each study product. |
Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
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Toissijaiset tulostoimenpiteet
Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Area Under the Plasma Concentration-Time Curve From 0 to 168 Hours (AUC168h) of Semaglutide
Aikaikkuna: Pre-dose through 168 hours post-dose (Day 1 to Day 8) in each treatment period.
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AUC168h is the area under the plasma concentration-time curve of semaglutide from time zero to 168 hours after dosing. |
Pre-dose through 168 hours post-dose (Day 1 to Day 8) in each treatment period.
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Area Under the Plasma Concentration-Time Curve From Time Zero to Infinity (AUCinf) of Semaglutide
Aikaikkuna: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
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AUCinf is the area under the plasma concentration-time curve of semaglutide from time zero extrapolated to infinity, calculated by noncompartmental analysis. |
Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
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Apparent Clearance (CL/F) of Semaglutide
Aikaikkuna: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
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CL/F is the apparent clearance of semaglutide following subcutaneous administration, estimated using noncompartmental pharmacokinetic analysis. |
Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
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Apparent Volume of Distribution (Vz/F) of Semaglutide
Aikaikkuna: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
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Vz/F is the apparent volume of distribution of semaglutide during the terminal phase following subcutaneous administration, estimated using noncompartmental analysis. |
Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
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Time to Maximum Observed Plasma Concentration (Tmax) of Semaglutide
Aikaikkuna: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
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Tmax is the observed time required to reach the maximum plasma concentration (Cmax) of semaglutide after dosing. |
Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
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Terminal Elimination Half-Life (t1/2) of Semaglutide
Aikaikkuna: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
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The terminal elimination half-life of semaglutide is calculated as ln(2)/lambda z, where lambda z is the terminal elimination rate constant estimated from the plasma concentration-time profile. |
Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.
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Muut tulostoimenpiteet
Muut tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Number of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs)
Aikaikkuna: From the first administration through the post-study visit (Day 43 to Day 47 after the final administration).
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The number and percentage of participants experiencing adverse events and serious adverse events will be assessed. Adverse events will be summarized by severity, seriousness, and relationship to the study drug. |
From the first administration through the post-study visit (Day 43 to Day 47 after the final administration).
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Yhteistyökumppanit ja tutkijat
Sponsori
Sponsori
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Arvioitu)
Opiskelun aloitus
Ensisijainen valmistuminen (Arvioitu)
Ensisijainen valmistuminen
Opintojen valmistuminen (Arvioitu)
Opintojen valmistuminen
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Todellinen)
Ensimmäinen Lähetetty
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin päivitys julkaistu
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
Viimeksi vahvistettu
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Avainsanat
Muita asiaankuuluvia MeSH-ehtoja
Muut tutkimustunnusnumerot
Muut tutkimustunnusnumerot
- KUP-UI112-101
Yksittäisten osallistujien tietojen suunnitelma (IPD)
Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?
IPD-suunnitelman kuvaus
There is no current plan to share individual participant data (IPD) with external researchers. Study data will be managed by the sponsor in accordance with the study protocol, applicable regulations, and confidentiality requirements.
Lääke- ja laitetiedot, tutkimusasiakirjat
Tutkii yhdysvaltalaista FDA sääntelemää lääkevalmistetta
Tutkii yhdysvaltalaista FDA sääntelemää laitetuotetta
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