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Safety and Pharmacokinetics of UI112 Compared With UIC202611 in Healthy Adults

9 de noviembre de 2026 actualizado por: Korea United Pharm. Inc.

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.

Descripción general del estudio

Estado

Aún no reclutando

Descripción detallada

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.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

44

Fase

  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Min Kyu Park, MD, PhD
  • Número de teléfono: +82-43-269-8708
  • Correo electrónico: mk_park@cbnuhctc.com

Ubicaciones de estudio

    • North Chungcheong
      • Cheongju-si, North Chungcheong, Corea del Sur, 28644
        • Chungbuk National University Hospital
        • Contacto:
          • Chungbuk National University Hospital Clinical Trial Center
          • Número de teléfono: +82-43-269-7284
          • Correo electrónico: cbnuhctc2@naver.com

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

19 años a 64 años (Adulto)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Descripción

  • Inclusion Criteria:

    1. Healthy adult volunteers aged 19 years or older and younger than 65 years at screening.
    2. 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.
    3. Participants without congenital diseases or chronic diseases requiring treatment and without pathological symptoms or findings based on a medical examination.
    4. 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.
    5. 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.
  • Exclusion Criteria:

    1. Current or past history of clinically significant hepatic, renal, neurological, psychiatric, respiratory, endocrine, hematological, neoplastic, genitourinary, cardiovascular, gastrointestinal, musculoskeletal, or other clinically significant diseases.
    2. Pregnant women (positive urine human chorionic gonadotropin [HCG] test) or breastfeeding women.
    3. 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.
    4. History of skin diseases (e.g., burns or skin cancer) or skin transplantation that may affect the absorption of the investigational products.
    5. History of acute or chronic pancreatitis.
    6. Personal or family history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia type 2 (MEN2).
    7. Clinically significant abnormalities on a 12-lead ECG at screening, including any of the following:
  • QTc interval >450 ms in males or >460 ms in females.

  • PR interval >200 ms.

  • QRS duration >120 ms. 8. Clinically significant abnormalities in clinical laboratory tests at screening, including any of the following:

  • AST, ALT, ALP, gamma-GT, or total bilirubin >2 times the upper limit of normal (ULN).

  • Serum creatinine outside the reference range or estimated glomerular filtration rate (eGFR), calculated using the CKD-EPI equation, <60 mL/min/1.73 m².

  • Lipase or amylase >2 times the ULN.

  • 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:

  • Systolic blood pressure ≤90 mmHg or ≥150 mmHg.

  • Diastolic blood pressure ≤60 mmHg or ≥100 mmHg.

  • 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.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Otro
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación cruzada
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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.

Otros nombres:
  • UI112

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.

Otros nombres:
  • Wegovy
Experimental: 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.

Otros nombres:
  • UI112

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.

Otros nombres:
  • Wegovy

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Area Under the Plasma Concentration-Time Curve From Time Zero to the Last Quantifiable Concentration (AUCt) of Semaglutide
Periodo de tiempo: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.

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.
Maximum Observed Plasma Concentration (Cmax) of Semaglutide
Periodo de tiempo: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.

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.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Area Under the Plasma Concentration-Time Curve From 0 to 168 Hours (AUC168h) of Semaglutide
Periodo de tiempo: Pre-dose through 168 hours post-dose (Day 1 to Day 8) in each treatment period.

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.
Area Under the Plasma Concentration-Time Curve From Time Zero to Infinity (AUCinf) of Semaglutide
Periodo de tiempo: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.

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.
Apparent Clearance (CL/F) of Semaglutide
Periodo de tiempo: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.

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.
Apparent Volume of Distribution (Vz/F) of Semaglutide
Periodo de tiempo: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.

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.
Time to Maximum Observed Plasma Concentration (Tmax) of Semaglutide
Periodo de tiempo: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.

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.
Terminal Elimination Half-Life (t1/2) of Semaglutide
Periodo de tiempo: Pre-dose through 504 hours post-dose (Day 1 to Day 22) in each treatment period.

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.

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Number of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs)
Periodo de tiempo: From the first administration through the post-study visit (Day 43 to Day 47 after the final administration).

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).

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de enero de 2027

Finalización primaria (Estimado)

1 de noviembre de 2027

Finalización del estudio (Estimado)

1 de diciembre de 2027

Fechas de registro del estudio

Enviado por primera vez

28 de octubre de 2026

Primero enviado que cumplió con los criterios de control de calidad

9 de noviembre de 2026

Publicado por primera vez (Actual)

13 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

13 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

9 de noviembre de 2026

Última verificación

1 de noviembre de 2026

Más información

Términos relacionados con este estudio

Términos MeSH relevantes adicionales

Otros números de identificación del estudio

  • KUP-UI112-101

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

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.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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