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Pharmacokinetics, Safety and Tolerability of CKD-387 10/500mg BE Phase1

6. november 2019 oppdatert av: Chong Kun Dang Pharmaceutical

An Open-label, Rendomized, Single-dose Crossover Study to Evaluate the Pharmacokinetics, Safety and Tolerability of CKD-387 in Healthy Subjects.

The purpose of this study is to evaluate the pharmacokinetics, safety and tolerability of CKD-387

Studieoversikt

Detaljert beskrivelse

An open-label, randomized, single-dose crossover study to evaluate the pharmacokinetics, safety and tolerability of CKD-387 in helalthy subjects.

Studietype

Intervensjonell

Registrering (Faktiske)

58

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Seongbuk-Gu
      • Seoul, Seongbuk-Gu, Korea, Republikken
        • Korea University Anam Hospital

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

19 år til 45 år (Voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  1. Healthy adult older than 19 years and less than 45 years at the time of screening.
  2. BMI 18.5~29.9 kg/m2 and body weight more than 50kg.
  3. Subjects who have consented to the use of appropriate double- pregnancy contraceptive methods up to one months after the last investigational product and not to provide sperm for men.
  4. Subjects who sign on an informed consent form willingly.

Exclusion Criteria:

  1. Subjects who have a clinically significant disease or medical history such as respiratory, hepatic, kidneys, blood, gastrointestinal, endocrine, immune system, skin, nervous and mental disease.
  2. Subjects who have acute disease within 28 days prior to the first administration.
  3. Subjects who have history that may affect the ADME.
  4. Subjects who have medical history or medical abuse history of hypersensitivity from SGLT inhibitors or Biguanides including Metformin or other medications(Aspirin, Antibiotics etc.).
  5. Subjects who have clinically significant chronic disease.
  6. Subjects with genetic problems such as galactose intolerance, Lapp lactase deficiency or glucose-galactose mal-absorption.
  7. Subjects whose laboratory test result are same as below;

    • AST,ALT > UNL(Upper Normal Limit)x3
    • Fasting glucose level out of 70-125mg/dl
    • Creatinine clearance is lower than 80mL/min which is calcuated by Cockcroft-Gault formulation.
    • QT>450msec
    • Positive urine hCG(female).
  8. Subjects whoes blood pressure exceeds out of normal range as below at screening.

    • SBP : over 100mmHg, under 160mmHg
    • DBP : over 60mmHg, under 100mmHg
  9. Subjects who have been found to be positive in serological tests(HBs antigen, HCV antibody and HIV antibody).
  10. Subjects who took ETC(Ethical Drug), oriental medicine within 2 weeks prior to the first administration of investigational products.
  11. Subjects who took OTC(Over-the-counter Drug, including korean galenical drug) within 10 days prior to the first administration of investigational products.
  12. Subjects who have allergic disease which has clinical significance(But, light allergic rhinitis and ligth allergic dermatitis which do not need medication is exceptional).
  13. Subjects who can not eat standard meals provided by the institution.
  14. Subjects who donated whole blood within 60 days, donated the blood components within 20 days prior to the first administration of investigational products.
  15. Subjects who received blood transfusion within 30 days prior to the first administration of investigational products.
  16. Subjects who were participated in the other clinical trial within 90 days prior to the first administration of investigational products.
  17. Subjects who took medication for the induction and inhibition of metabolizing enzymes such as barbiturate drugs within 6months prior to the first administration of investigational products.
  18. Subjects who have had abnormal diets that can affect the ADME of the drug within 30 days prior to the first administration of investigational products. (Ingestion of grapefruit juice>1L/day or Caffein>5Cups/day).
  19. Subjects who have took regular alcohol(alcohol>30g/day) prior to the first administration of investigational products.
  20. Subjects who smoked more than 10 cigarettes per day prior 3months to the first administration of investigational products or cannot discontinue smoking during the clinical trial.
  21. Subjects who is determined unsuitable to participate in this clinical trial by the investigator.
  22. Lactating Women.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Annen
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: PartA, Treatment-1
Period 1 : Reference drug Period 2 : Test drug
Once a day. Under fasting condition
Andre navn:
  • PartA, Test(CKD-387 10/500mg)
Eksperimentell: PartA, Treatment-2
Period 1 : Test drug Period 2 : Reference drug
Once a day. Under fasting condition
Andre navn:
  • PartA, Test(CKD-387 10/500mg)
Eksperimentell: PartB, Treatment-1
Period 1 : Reference drug Period 2 : Test drug
Once a day. Under fed condition
Andre navn:
  • PartB, Test(CKD-387 10/500mg)
Eksperimentell: PartB, Treatment-2
Period 1 : Test drug Period 2 : Reference drug
Once a day. Under fed condition
Andre navn:
  • PartB, Test(CKD-387 10/500mg)

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Part A : Cmax under fasting condition
Tidsramme: 0(predose)~48 hours
Maximum concentration of the dapagliflozin
0(predose)~48 hours
Part A : Cmax under fasting condition
Tidsramme: 0(predose)~48 hours
Maximum concentration of the metformin
0(predose)~48 hours
Part A : AUClast under fasting condition
Tidsramme: 0(predose)~48 hours
Area Under Curve(last) of the dapagliflozin
0(predose)~48 hours
Part A : AUClast under fasting condition
Tidsramme: 0(predose)~48 hours
Area Under Curve(last) of the metformin
0(predose)~48 hours
Part B : Cmax under fed condition
Tidsramme: 0(predose)~48 hours
Maximum concentration of the metformin
0(predose)~48 hours
Part B : AUClast under fed condition
Tidsramme: 0(predose)~48 hours
Area Under Curve(last) of the metformin
0(predose)~48 hours

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Part A : AUCinf under fasting condition
Tidsramme: 0(predose)~48 hours
Area Under Curve(infinit) of the dapagliflozin
0(predose)~48 hours
Part A : AUCinf under fasting condition
Tidsramme: 0(predose)~48 hours
Area Under Curve(infinit) of the metformin
0(predose)~48 hours
Part A : Tmax under fasting condition
Tidsramme: 0(predose)~48 hours
Time of maximum concentration of the dapagliflozin
0(predose)~48 hours
Part A : Tmax under fasting condition
Tidsramme: 0(predose)~48 hours
Time of maximum concentration of the metformin
0(predose)~48 hours
Part A : t1/2 under fasting condition
Tidsramme: 0(predose)~48 hours
Half life of the dapagliflozin
0(predose)~48 hours
Part A : t1/2 under fasting condition
Tidsramme: 0(predose)~48 hours
Half life of the metformin
0(predose)~48 hours
Part B : AUCinf under fed condition
Tidsramme: 0(predose)~48 hours
Area Under Curve(infinit) of the metformin
0(predose)~48 hours
Part B : Tmax under fed condition
Tidsramme: 0(predose)~48 hours
Time of Maximum concentration of the metformin
0(predose)~48 hours
Part B : t1/2 under fed condition
Tidsramme: 0(predose)~48 hours
Half life of the metformin
0(predose)~48 hours

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Ji-Young Park, M.D, Ph.D, Korea University Anam Hospital / Seoul, Seongbuk-Gu, South Korea

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

6. august 2019

Primær fullføring (Faktiske)

30. august 2019

Studiet fullført (Faktiske)

2. oktober 2019

Datoer for studieregistrering

Først innsendt

6. november 2019

Først innsendt som oppfylte QC-kriteriene

6. november 2019

Først lagt ut (Faktiske)

7. november 2019

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

7. november 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

6. november 2019

Sist bekreftet

1. november 2019

Mer informasjon

Begreper knyttet til denne studien

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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