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Evaluation of the Pharmacokinetics/Pharmacodynamics and Safety/Tolerability of IN-C005 and IN-A001 in Healthy Caucasians

10 de mayo de 2022 actualizado por: HK inno.N Corporation

A Randomized, Open-label, Multiple Dosing, Cross-over Phase 1 Clinical Trial to Evaluate Pharmacokinetics/Pharmacodynamics and Safety/Tolerability of IN-C005 and IN-A001 After Oral Administration in Healthy Caucasian Subjects

The purpose of this study is to evaluate pharmacokinetics/pharmacodynamics and safety/tolerability of IN-C005 and IN-A001 after oral administration in healthy Caucasian subjects.

Descripción general del estudio

Descripción detallada

[Part 1] To evaluate the pharmacokinetic (PK)/pharmacodynamic (PD) profiles and safety/tolerability of 100 mg IN-C005 versus 100 mg IN-A001 after multiple oral dosing in healthy Caucasian subjects

[Part 2] To evaluate the PK/PD profiles and safety/tolerability of 50 mg IN-C005 versus 75 mg IN-C005 after multiple oral dosing in healthy Caucasian subjects

Tipo de estudio

Intervencionista

Inscripción (Actual)

20

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.

Ubicaciones de estudio

      • Seoul, Corea, república de, 03080
        • Seoul National University Hopsital
    • Jongro Gu
      • Seoul, Jongro Gu, Corea, república de, 03080
        • Seoul National University Hospital

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 50 años (Adulto)

Acepta Voluntarios Saludables

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  1. Is healthy Caucasian adult aged 19 to 50 years (inclusive) at the time of signing the informed consent form (ICF) (A Caucasian is defined as a European who was born in Europe, has the duration of residence outside of Europe less than 10 years, and both of whose parents and grandparents are European-born).
  2. Has ≥ 18.0 and ≤ 30.0 kg/m2 of body mass index (BMI) with a body weight (BW) ≥ 55.0 kg at screening.
  3. Has a negative result in serum Helicobacter pylori IgG antibody test.
  4. Decides to participate voluntarily in the study after being fully informed of and understanding the study completely, and provides his/her written informed consent prior to screening procedure.
  5. Is eligible for this study in the opinion of the investigator based on the results of physical examination, clinical laboratory tests, interview, etc.

Exclusion Criteria:

  1. Has a history or current evidence of clinically significant disorder of hepatic, renal, nervous, respiratory, endocrine, hemato-oncologic, cardiovascular, urinary, and/or psychiatric system.
  2. Has a history or current evidence of gastrointestinal disease that may affect the safety and PD assessments for study treatment (e.g., gastrointestinal ulcer, gastritis, gastric cramp, gastroesophageal reflux disease, and Crohn's disease) or a history of gastrointestinal surgery (except for simple appendectomy or herniotomy).
  3. Has a history or current evidence of clinically significant hypersensitivity to study drugs or any ingredient of proton pump inhibitors and other drugs (such as aspirin and antibiotics).
  4. Has a positive result on serology tests (for hepatitis B, human immunodeficiency virus [HIV], and hepatitis C).
  5. Has a blood level of total bilirubin, AST (GOT), or ALT (GPT) > 1.5 X upper limit of normal (ULN) based on screening procedures including repeated ones.
  6. Has a calculated eGFR per MDRD equation < 60 mL/min/1.73 m2 based on screening procedures including repeated ones.
  7. Has systolic blood pressure (SBP) of < 90 mmHg or > 140 mmHg, diastolic blood pressure (DBP) of < 50 mmHg or > 95 mmHg, or pulse rate (PR) of < 45 beats/min or > 100 beats/min on vital signs as measured in sitting position after taking a rest for at least 5 minutes at screening.
  8. Has an anatomical disorder that precludes insertion and maintenance of intragastric pH meter catheter or is expected to be intolerable to insertion of intragastric pH meter catheter.
  9. Has a history of drug abuse or has a positive response to drug abuse on urine drug screening test.
  10. Has received any prescription drug or herbal medication within 2 weeks of or any over-the-counter (OTC) drug, dietary supplements, or vitamins within 1 week of scheduled first dose or is expected to receive such medication during the study (Note: a subject may participate in the study at the discretion of the investigator provided the subject meets all the other criteria).
  11. Has participated and received an investigational agent in another clinical trial or bioequivalence study within 6 months prior to the first dose of study treatment (Note: This is not applied to participation in another part of this study).
  12. Has donated whole blood within 2 months prior to the scheduled first dose, or has donated blood components or received transfusion within a month prior to the scheduled first dose.
  13. Has excessive caffeine intake (> 5 units/day), continues the use of alcohol (> 21 units/week, 1 unit = 10 g of pure alcohol), or is unable to stop drinking during hospitalization period.
  14. Has a positive result for cotinine on urine drug screening test or is unable to stop smoking throughout the study.
  15. Is unable to avoid grapefruit-containing foods during the time from 24 hours (hrs) before hospitalization to discharge in Period 1 and Period 2, respectively.
  16. Is unable to avoid caffeine-containing foods (e.g., coffee, tea [red tea, green tee, etc.], soda, coffee milk, and nutritive tonic drink) during the time from 24 hrs before hospitalization to discharge Period 1 and Period 2, respectively.
  17. For all women of childbearing potential (WOCBP) excluding those on amenorrhea for at least 12 months and those who underwent surgical sterilization (bilateral tubal ligation, bilateral oophorectomy, or hysterectomy), has a positive result for pregnancy test (urine hCG) performed prior to the first dose of study treatment or is pregnant or breastfeeding.
  18. Is unable to use a medically acceptable contraceptive method throughout the study. Medically acceptable contraceptive methods include:

    • Use of an intrauterine device with a proven birth control failure rate by the subject or subject's spouse (or partner)
    • Use of (male or female) barrier method with spermicide
    • Surgical sterilization (vasectomy, salpingectomy, tubal ligation, hysterectomy) of the subject or subject's spouse (or partner)
  19. Is determined ineligible for study participation by the investigator for other reasons such as clinical laboratory abnormalities.

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: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación cruzada
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Treatment AB
Participants will be randomized to receive IN-C005 Y mg (Treatment A) and IN-A001 Y mg (Treatment B) sequentially in a two-period sequence. There will be a washout period of at least 14 days between Period 1 and Period 2.
Oral tablet
Oral capsule
Experimental: Treatment BA
Participants will be randomized to receive IN-A001 Y mg and IN-C005 Y mg sequentially in a two-period sequence. There will be a washout period of at least 14 days between Period 1 and Period 2.
Oral tablet
Oral capsule
Experimental: Treatment CD
Participants will be randomized to receive IN-C005 Z mg (Treatment C) and IN-C005 X mg (Treatment D) sequentially in a two-period sequence. There will be a washout period of at least 14 days between Period 1 and Period 2.
Oral capsule
Oral capsule
Experimental: Treatment DC
Participants will be randomized to receive IN-C005 X mg and IN-C005 Z mg sequentially in a two-period sequence. There will be a washout period of at least 14 days between Period 1 and Period 2.
Oral capsule
Oral capsule

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Cmax
Periodo de tiempo: Day 1, Day 22
PK: Maximum concentration of drug in plasma
Day 1, Day 22
AUClast
Periodo de tiempo: Day 1, Day 22
PK: Area under the plasma drug concentration-time curve from 0 to last point of measurable concentration
Day 1, Day 22
Cmax,ss
Periodo de tiempo: Day 7 and Day 28
PK: Maximum (peak) steady-state plasma drug concentration during a dosage interval
Day 7 and Day 28
AUCtau,ss
Periodo de tiempo: Day 7 and Day 28
PK: Area under the plasma drug concentration-time curve for a dosing interval at steady state
Day 7 and Day 28
Percent duration of pH ≥4 in 24 hrs (duration %)
Periodo de tiempo: Day 1, Day 22
PD: pH parameter
Day 1, Day 22
Percent duration of pH ≥4 in 24 hrs (duration %)
Periodo de tiempo: Day 7, Day 28
PD: pH parameter
Day 7, Day 28
Change from baseline in percent duration of pH ≥4 in 24 hrs
Periodo de tiempo: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
AUCinf
Periodo de tiempo: Day 1, Day 22
PK: Area under the plasma drug concentration-time curve from time 0 to infinity
Day 1, Day 22
Tmax
Periodo de tiempo: Day 1, Day 22
PK: The time of peak concentration
Day 1, Day 22
t1/2
Periodo de tiempo: Day 1, Day 22
PK: Terminal half-life
Day 1, Day 22
CL/F
Periodo de tiempo: Day 1, Day 22
PK: Apparent Clearance
Day 1, Day 22
Vd/F
Periodo de tiempo: Day 1, Day 22
PK: Apparent volume of distribution after extravascular administration
Day 1, Day 22
Tmax,ss
Periodo de tiempo: Day 7, Day 28
PK: Time to reach Cmax
Day 7, Day 28
t1/2,ss
Periodo de tiempo: Day 7, Day 28
PK: Apparent first order terminal elimination half-life
Day 7, Day 28
Cmin,ss
Periodo de tiempo: Day 7, Day 28
PK: Minimum observed non zero concentration between dose time and dose time + dosing interval, tau
Day 7, Day 28
Cavg,ss
Periodo de tiempo: Day 7, Day 28
PK: The average concentration at steady state, calculated as the ratio of AUCtau to the dosing interval, tau
Day 7, Day 28
CLss/F
Periodo de tiempo: Day 7, Day 28
PK: The total body clearance at steady state after oral administration
Day 7, Day 28
Vd,ss/F
Periodo de tiempo: Day 7, Day 28
PK: Apparent volume of distribution after extravascular administration in steady state
Day 7, Day 28
PTF
Periodo de tiempo: Day 7, Day 28
PK: Peak to trough fluctuation
Day 7, Day 28
R
Periodo de tiempo: Day 7, Day 28
PK: Accumulation ratio
Day 7, Day 28
Percent duration of pH ≥3 in 24 hrs
Periodo de tiempo: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Change from baseline in percent duration of pH ≥3 in 24 hrs
Periodo de tiempo: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Percent duration of pH ≥6 in 24 hrs
Periodo de tiempo: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Change from baseline in percent duration of pH ≥6 in 24 hrs
Periodo de tiempo: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Mean and median pH in 24 hrs
Periodo de tiempo: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Change from baseline in mean pH in 24 hrs
Periodo de tiempo: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Change from baseline in median pH in 24 hrs
Periodo de tiempo: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
AUEGlast
Periodo de tiempo: Day 1, Day 7, Day 22, Day 28
PD(Gastrin): Area under the concentration-time curve of Serum Gastrin from 0 to last point of quantifiable concentration
Day 1, Day 7, Day 22, Day 28
Gmax
Periodo de tiempo: Day 1, Day 7, Day 22, Day 28
Gastrin: Maximum gastrin level
Day 1, Day 7, Day 22, Day 28
ΔAUEGlast
Periodo de tiempo: Day 1, Day 7, Day 22, Day 28
PD(Gastrin): Change from baseline in AUEGlast
Day 1, Day 7, Day 22, Day 28
ΔGmax
Periodo de tiempo: Day 1, Day 7, Day 22, Day 28
PD(Gastrin): Change from baseline in Gmax
Day 1, Day 7, Day 22, Day 28

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Investigador principal: In-Jin Jang, MD, Ph.D, Clinical Pharmacology and Therapeutics, Seoul National University Hospital

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 (Actual)

6 de septiembre de 2021

Finalización primaria (Actual)

18 de noviembre de 2021

Finalización del estudio (Actual)

30 de noviembre de 2021

Fechas de registro del estudio

Enviado por primera vez

5 de julio de 2021

Primero enviado que cumplió con los criterios de control de calidad

6 de agosto de 2021

Publicado por primera vez (Actual)

13 de agosto de 2021

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

16 de mayo de 2022

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

10 de mayo de 2022

Última verificación

1 de agosto de 2021

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • IN_BTK_102

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

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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