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

10 mei 2022 bijgewerkt door: 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.

Studie Overzicht

Gedetailleerde beschrijving

[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

Studietype

Ingrijpend

Inschrijving (Werkelijk)

20

Fase

  • Fase 1

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

      • Seoul, Korea, republiek van, 03080
        • Seoul National University Hopsital
    • Jongro Gu
      • Seoul, Jongro Gu, Korea, republiek van, 03080
        • Seoul National University Hospital

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

19 jaar tot 50 jaar (Volwassen)

Accepteert gezonde vrijwilligers

Ja

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

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.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Crossover-opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: 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
Experimenteel: 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
Experimenteel: 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
Experimenteel: 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

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Cmax
Tijdsspanne: Day 1, Day 22
PK: Maximum concentration of drug in plasma
Day 1, Day 22
AUClast
Tijdsspanne: 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
Tijdsspanne: Day 7 and Day 28
PK: Maximum (peak) steady-state plasma drug concentration during a dosage interval
Day 7 and Day 28
AUCtau,ss
Tijdsspanne: 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 %)
Tijdsspanne: Day 1, Day 22
PD: pH parameter
Day 1, Day 22
Percent duration of pH ≥4 in 24 hrs (duration %)
Tijdsspanne: Day 7, Day 28
PD: pH parameter
Day 7, Day 28
Change from baseline in percent duration of pH ≥4 in 24 hrs
Tijdsspanne: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
AUCinf
Tijdsspanne: Day 1, Day 22
PK: Area under the plasma drug concentration-time curve from time 0 to infinity
Day 1, Day 22
Tmax
Tijdsspanne: Day 1, Day 22
PK: The time of peak concentration
Day 1, Day 22
t1/2
Tijdsspanne: Day 1, Day 22
PK: Terminal half-life
Day 1, Day 22
CL/F
Tijdsspanne: Day 1, Day 22
PK: Apparent Clearance
Day 1, Day 22
Vd/F
Tijdsspanne: Day 1, Day 22
PK: Apparent volume of distribution after extravascular administration
Day 1, Day 22
Tmax,ss
Tijdsspanne: Day 7, Day 28
PK: Time to reach Cmax
Day 7, Day 28
t1/2,ss
Tijdsspanne: Day 7, Day 28
PK: Apparent first order terminal elimination half-life
Day 7, Day 28
Cmin,ss
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: Day 7, Day 28
PK: The total body clearance at steady state after oral administration
Day 7, Day 28
Vd,ss/F
Tijdsspanne: Day 7, Day 28
PK: Apparent volume of distribution after extravascular administration in steady state
Day 7, Day 28
PTF
Tijdsspanne: Day 7, Day 28
PK: Peak to trough fluctuation
Day 7, Day 28
R
Tijdsspanne: Day 7, Day 28
PK: Accumulation ratio
Day 7, Day 28
Percent duration of pH ≥3 in 24 hrs
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
AUEGlast
Tijdsspanne: 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
Tijdsspanne: Day 1, Day 7, Day 22, Day 28
Gastrin: Maximum gastrin level
Day 1, Day 7, Day 22, Day 28
ΔAUEGlast
Tijdsspanne: Day 1, Day 7, Day 22, Day 28
PD(Gastrin): Change from baseline in AUEGlast
Day 1, Day 7, Day 22, Day 28
ΔGmax
Tijdsspanne: Day 1, Day 7, Day 22, Day 28
PD(Gastrin): Change from baseline in Gmax
Day 1, Day 7, Day 22, Day 28

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

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

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

6 september 2021

Primaire voltooiing (Werkelijk)

18 november 2021

Studie voltooiing (Werkelijk)

30 november 2021

Studieregistratiedata

Eerst ingediend

5 juli 2021

Eerst ingediend dat voldeed aan de QC-criteria

6 augustus 2021

Eerst geplaatst (Werkelijk)

13 augustus 2021

Updates van studierecords

Laatste update geplaatst (Werkelijk)

16 mei 2022

Laatste update ingediend die voldeed aan QC-criteria

10 mei 2022

Laatst geverifieerd

1 augustus 2021

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • IN_BTK_102

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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