Denne side blev automatisk oversat, og nøjagtigheden af ​​oversættelsen er ikke garanteret. Der henvises til engelsk version for en kildetekst.

A Study to Compare the Pharmacokinetics of BR9003A and BR9003 in Healthy Adult Subjects

19. juli 2021 opdateret af: Boryung Pharmaceutical Co., Ltd

A Randomized, Open-label, Three-treatment, Six-sequence, Three-period, Crossover Clinical Study to Compare the Pharmacokinetic Characteristics Between Twice Daily Administration of BR9003A and Once Daily Administration of BR9003 in Healthy Adult Subjects

The purpose of this study is to evaluate the pharmacokinetics and safety of oral administration of BR9003 compared with BR9003A in healthy adult subjects

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Detaljeret beskrivelse

A total of 24 subjects will be randomized into 6 sequence groups. The Investigational Products wil be according to the treatment group (A,B,C) assigned to each sequence group in Period 1, Period 2 and Period 3.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

24

Fase

  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

19 år til 55 år (Voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  1. Healthy adults aged 19 to 55 years at screening
  2. Those who weigh at least 50 kg at the time of screening and have a calculated body mass index (BMI) within the range of 18.0 to 29.0 kg/m2
  3. Determined to be eligible as subjects through physical examination and interview conducted in accordance with this protocol. In other words, those who have no congenital or chronic diseases and have no abnormal symptoms or findings based on medical examination results within the last 3 years
  4. Determined to be eligible as subjects as a result of clinical laboratory tests and electrocardiography performed according to this protocol
  5. Voluntarily decide to participate in the study and provide written consent to follow the study directions after listening to and fully understanding the detailed explanation on this study

Exclusion Criteria:

  1. Those who have clinically significant diseases or a history of the diseases associated with the cardiovascular system, respiratory system, liver, kidney, nervous system, endocrine system, blood/tumor, psychiatric diseases, or urinary system
  2. Those who have hypersensitivity reactions or a history of clinically significant hypersensitivity reactions to drugs containing varenicline, or drugs containing the same class ingredients, or other drugs
  3. Those with clinically significant hypotension (systolic blood pressure ≤ 90mmHg) or hypertension (systolic blood pressure ≥ 150mmHg or diastolic blood pressure ≥ 95mmHg) at the time of screening
  4. Those with a history of gastrointestinal diseases (e.g., Crohn's disease, ulcer, etc.) or gastrointestinal surgery (however, simple appendectomy or hernia repair are excluded) that may affect the absorption of drugs
  5. Any of the following results in the screening tests

    • AST or ALT > 2 times the upper limit of the normal range
    • Total bilirubin > 2.0 mg/dL
    • Estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73m2
  6. Those who continue to drink alcohol (>21 units/week; 1 unit = 10 g = 12.5 mL of pure alcohol), or are unable to abstain from drinking during the clinical study period
  7. Those who continue to smoke (>10 cigarettes/day) or cannot stop smoking during hospitalization during the clinical trial period
  8. Those who have participated in another clinical trial or bioequivalence test (the last day of administration of the investigational product or bioequivalence test drug) within 6 months prior to the first administration date
  9. Those who have donated whole blood within 60 days prior to the first day of administration or donated blood components (apheresis) within 30 days prior to the first day of administration or who have received a blood transfusion within 30 days
  10. Those who took any prescription drugs or herbal medicines within 14 days prior to the first day of administration or any over-the-counter (OTC) drugs within 7 days prior to the first day of administration (however, if other conditions are appropriate according to the judgment of the investigator, they may participate in the clinical trial.)
  11. Those who took drugs inducing and inhibiting drug-metabolizing enzymes, such as barbital, within 30 days prior to the study initiation
  12. Those who have been on a diet (especially grapefruit juice or its products) that may affect the absorption, distribution, metabolism, and excretion of the drug within 7 days prior to the first day of administration
  13. Pregnant woman, potentially pregnant woman, or breast-feeding woman
  14. Those who do not agree to rule out the possibility of their and their spouses' or sexual partners' pregnancy using a medically acceptable methods of contraception* throughout the entire period from the date of the first administration of the investigational product to the end of the clinical trial
  15. Those who are unwilling or unable to comply with the dietary and lifestyle guidelines required for the clinical trial
  16. Those who have clinically significant abnormalities in the results of other clinical laboratory tests or who have been determined by the investigator to be ineligible to participate in the clinical trial due to other reasons (e.g., non-compliance with instructions, uncooperative attitude, etc.)

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Crossover opgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Sekvens 1

Undersøgelsesprodukterne vil blive administreret i overensstemmelse med de behandlingsgrupper (A,B,C), der er tildelt hver sekvensgruppe i periode 1, periode 2 og periode 3.

*sekvens 1: A-B-C

Treatment group B:

Once-daily oral administration of one BR9003 2mg tablet in the fasting state.

Treatment group C:

Once-daily oral administration of one BR9003 2mg tablet after a meal(high-fat meal) 30 minutes before the scheduled time of administration and finishing it.

Treatment group A:

Twice-daily oral administration of one BR9003A 1mg tablet in the fasting state

Eksperimentel: Sekvens 2

Undersøgelsesprodukterne vil blive administreret i overensstemmelse med de behandlingsgrupper (A,B,C), der er tildelt hver sekvensgruppe i periode 1, periode 2 og periode 3.

*sekvens 2: A-C-B

Treatment group B:

Once-daily oral administration of one BR9003 2mg tablet in the fasting state.

Treatment group C:

Once-daily oral administration of one BR9003 2mg tablet after a meal(high-fat meal) 30 minutes before the scheduled time of administration and finishing it.

Treatment group A:

Twice-daily oral administration of one BR9003A 1mg tablet in the fasting state

Eksperimentel: Sekvens 3

Undersøgelsesprodukterne vil blive administreret i overensstemmelse med de behandlingsgrupper (A,B,C), der er tildelt hver sekvensgruppe i periode 1, periode 2 og periode 3.

*sekvens 3: B-A-C

Treatment group B:

Once-daily oral administration of one BR9003 2mg tablet in the fasting state.

Treatment group C:

Once-daily oral administration of one BR9003 2mg tablet after a meal(high-fat meal) 30 minutes before the scheduled time of administration and finishing it.

Treatment group A:

Twice-daily oral administration of one BR9003A 1mg tablet in the fasting state

Eksperimentel: Sekvens 4

Undersøgelsesprodukterne vil blive administreret i overensstemmelse med de behandlingsgrupper (A,B,C), der er tildelt hver sekvensgruppe i periode 1, periode 2 og periode 3.

*sekvens 4: B-C-A

Treatment group B:

Once-daily oral administration of one BR9003 2mg tablet in the fasting state.

Treatment group C:

Once-daily oral administration of one BR9003 2mg tablet after a meal(high-fat meal) 30 minutes before the scheduled time of administration and finishing it.

Treatment group A:

Twice-daily oral administration of one BR9003A 1mg tablet in the fasting state

Eksperimentel: Sekvens 5

Undersøgelsesprodukterne vil blive administreret i overensstemmelse med de behandlingsgrupper (A,B,C), der er tildelt hver sekvensgruppe i periode 1, periode 2 og periode 3.

*sekvens 5: C-A-B

Treatment group B:

Once-daily oral administration of one BR9003 2mg tablet in the fasting state.

Treatment group C:

Once-daily oral administration of one BR9003 2mg tablet after a meal(high-fat meal) 30 minutes before the scheduled time of administration and finishing it.

Treatment group A:

Twice-daily oral administration of one BR9003A 1mg tablet in the fasting state

Eksperimentel: Sekvens 6

Undersøgelsesprodukterne vil blive administreret i overensstemmelse med de behandlingsgrupper (A,B,C), der er tildelt hver sekvensgruppe i periode 1, periode 2 og periode 3.

*sekvens 6: C-B-A

Treatment group B:

Once-daily oral administration of one BR9003 2mg tablet in the fasting state.

Treatment group C:

Once-daily oral administration of one BR9003 2mg tablet after a meal(high-fat meal) 30 minutes before the scheduled time of administration and finishing it.

Treatment group A:

Twice-daily oral administration of one BR9003A 1mg tablet in the fasting state

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
AUCt
Tidsramme: 0-72 hours after administration
Area under the plasma drug concentration-time curve from 0 to time t of BR9003 and BR9003A
0-72 hours after administration
Cmax
Tidsramme: 0-72 hours after administration
Maximum concentration of drug in plasma of BR9003 and BR9003A
0-72 hours after administration

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

25. marts 2021

Primær færdiggørelse (Faktiske)

4. maj 2021

Studieafslutning (Faktiske)

18. maj 2021

Datoer for studieregistrering

Først indsendt

14. april 2021

Først indsendt, der opfyldte QC-kriterier

14. april 2021

Først opslået (Faktiske)

15. april 2021

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

20. juli 2021

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

19. juli 2021

Sidst verificeret

1. juli 2021

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • BR-VRNS-CT-102

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Abonner