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A Clinical Trial to Investigate the Pharmacokinetics and Safety/Tolerability of CKD-386 in Healthy Adult Volunteers

8. januar 2020 oppdatert av: Chong Kun Dang Pharmaceutical

Phase I Clinical Trial to Compare the Pharmacokinetics and Tolerability of CKD-386 With Co-administration of D012, D326, and D337 in Healthy Adult Volunteers

The purpose of this study is to evaluate the pharmacokinetics and Safety/Tolerability of CKD-386

Studieoversikt

Detaljert beskrivelse

Phase I clinical trial to compare the pharmacokinetics and tolerability of CKD-386 with co-administration of D012, D326, and D337 in healthy adult volunteers

Studietype

Intervensjonell

Registrering (Forventet)

30

Fase

  • Fase 1

Kontakter og plasseringer

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

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 og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  1. Those who are over 19 years old at the screening visit
  2. Those who weigh more than 50kg (45kg or more for women) at the screening visit and have a body mass index (BMI) within the range of 18-30kg/m^2
  3. Those who meet the following conditions of blood pressure measured in a sitting position after sufficient rest at the screening visit

    • Systolic blood pressure: 90mmHg or more and 139mmHg or less
    • Diastolic blood pressure: 60mmHg or more and 89mmHg or less
  4. Those who no congenital or chronic disease based on screening and no pathological symptoms or findings in medical examination results (e.g. EEG, ECG, chest and gastroscopy or gastrointestinal radiographs, if necessary)
  5. The person in charge of the examination (or authorized test physician) who has determined that the test subject is suitable for the diagnostic test and electrocardiogram test such as hematology test, blood chemistry test, serology test and urine test performed according to the characteristics of the investigational drug product
  6. Persons agreeing to exclude the possibility of pregnancy using appropriate contraceptive methods and not providing sperm or eggs from the date of first administration of the investigational drug to the 14th day after the last administration of the investigational drug

Exclusion Criteria:

  1. Those who participated in other clinical trials (including bioequivalence studies) within 6 months before the first dose and received the investigational drug
  2. Those who used drugs that induce and inhibit metabolic enzymes, such as barbital drugs, within one month before the first dose, or who used drugs that may interfere with this test within 10 days before the first dose
  3. Those who have donated whole blood within 2 months before the first dose or component donation within 1 month, or have transfused within 1 month
  4. Those who have had a history of gastrointestinal resection that may affect the absorption of the investigational drug (except appendectomy and hernia surgery)
  5. A person who meets the following conditions within one month before the first administration date

    • Excess alcohol: 21 cups / week for men and 14 cups / week for women.

      [1 glass = 50 mL of shochu or 30 mL of liquor or 250 mL of beer]

    • Smokers exceeding 20 cigarettes per day
  6. Patients with the following diseases

    • Patients with hypersensitivity to the main constituents or components of the investigational drug
    • Severe hepatic impairment, biliary atresia or cholestasis
    • Patients with hereditary angioedema or with a history of angioedema in the treatment of ACE inhibitors or angiotensin II receptor antagonists
    • Diabetes mellitus
    • Patients with moderate to severe renal impairment [glomerular filtration rate (eGFR) <60 mL / min / 1.73m^2]
    • Renal vascular hypertension patients
    • Patients with active liver disease, including unexplained persistent serum transaminase elevations or elevated serum transaminase elevations greater than three times the normal upper limit
    • Patients with myopathy or have a history of family or genetic history of myopathy
    • Hypothyroidism
    • If you have a history of muscle toxicity for other HMG-CoA converting enzymes or fibrate class drugs
  7. Genetic problems such as galactose intolerance, Lapp lactose deficiency, or glucose-galactose malabsorption
  8. person who is considered to be unsuitable for participation in this clinical trial for reasons other than the above selection / exclusion criteria.
  9. In the case of female volunteers, the suspected or lactating woman

Studieplan

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

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Crossover-oppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Group 1
Period 1: D012, D326, D337(3 tabs, once) / Period 2: CKD-386 F1(1 tab, once)/ Period 3: CKD-386 F2(1 tab, once)
A single oral dose of 1 tablet under fasting conditions for each period
Andre navn:
  • CKD-386 F1
A single oral dose of 1 tablet under fasting conditions for each period
Andre navn:
  • CKD-386 F2
A single oral dose of 3 tablets(D012, D326 and D337) under fasting conditions for each period
Eksperimentell: Group 2
Period 1: D012, D326, D337(3 tabs, once) / Period 2: CKD-386 F2(1 tab, once)/ Period 3: CKD-386 F1(1 tab, once)
A single oral dose of 1 tablet under fasting conditions for each period
Andre navn:
  • CKD-386 F1
A single oral dose of 1 tablet under fasting conditions for each period
Andre navn:
  • CKD-386 F2
A single oral dose of 3 tablets(D012, D326 and D337) under fasting conditions for each period
Eksperimentell: Group 3
Period 1: CKD-386 F1(1 tab, once) / Period 2: D012, D326, D337(3 tabs, once) Period 3: CKD-386 F2(1 tab, once)
A single oral dose of 1 tablet under fasting conditions for each period
Andre navn:
  • CKD-386 F1
A single oral dose of 1 tablet under fasting conditions for each period
Andre navn:
  • CKD-386 F2
A single oral dose of 3 tablets(D012, D326 and D337) under fasting conditions for each period
Eksperimentell: Group 4
Period 1: CKD-386 F1(1 tab, once) / Period 2: CKD-386 F2(1 tab, once) / Period 3: D012, D326, D337(3 tabs, once)
A single oral dose of 1 tablet under fasting conditions for each period
Andre navn:
  • CKD-386 F1
A single oral dose of 1 tablet under fasting conditions for each period
Andre navn:
  • CKD-386 F2
A single oral dose of 3 tablets(D012, D326 and D337) under fasting conditions for each period
Eksperimentell: Group 5
Period 1: CKD-386 F2(1 tab, once) / Period 2: D012, D326, D337(3 tabs, once)/ Period 3: CKD-386 F1(1 tab, once)
A single oral dose of 1 tablet under fasting conditions for each period
Andre navn:
  • CKD-386 F1
A single oral dose of 1 tablet under fasting conditions for each period
Andre navn:
  • CKD-386 F2
A single oral dose of 3 tablets(D012, D326 and D337) under fasting conditions for each period
Eksperimentell: Group 6
Period 1: CKD-386 F2(1 tab, once) / Period 2: CKD-386 F1(1 tab, once) / Period 3: D012, D326, D337(3 tabs, once)
A single oral dose of 1 tablet under fasting conditions for each period
Andre navn:
  • CKD-386 F1
A single oral dose of 1 tablet under fasting conditions for each period
Andre navn:
  • CKD-386 F2
A single oral dose of 3 tablets(D012, D326 and D337) under fasting conditions for each period

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
AUCt of each main component or metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337
Tidsramme: 0(predose)~72 hours
AUCt: Area under the concentration-time curve
0(predose)~72 hours
Cmax of each main component or metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337
Tidsramme: 0(predose)~72 hours
Cmax: Maximum plasma concentration of the drug
0(predose)~72 hours

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
AUCinf each main component or the metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337
Tidsramme: 0(predose)~72 hours
AUCinf: Area under the concentration-time curve from zero up to ∞
0(predose)~72 hours
tmax each main component or the metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337
Tidsramme: 0(predose)~72 hours
tmax: Time to maximum plasma concentration
0(predose)~72 hours
AUCt/AUCinf each main component or the metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337
Tidsramme: 0(predose)~72 hours
AUCt/AUCinf: AUCt/AUCinf Ratio
0(predose)~72 hours
t1/2 each main component or the metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337
Tidsramme: 0(predose)~72 hours
t1/2: Terminal elimination half-life
0(predose)~72 hours
AUCt of each main component or metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D326, D337
Tidsramme: 0(predose)~72 hours
AUCt: Area under the concentration-time curve
0(predose)~72 hours
Cmax of each main component or metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D326, D337
Tidsramme: 0(predose)~72 hours
Cmax: Maximum plasma concentration of the drug
0(predose)~72 hours

Samarbeidspartnere og etterforskere

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

Etterforskere

  • Hovedetterforsker: 70-4665-9174 70-4665-9174, H Plus Yangji Hospital

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 (Forventet)

1. februar 2020

Primær fullføring (Forventet)

4. mars 2020

Studiet fullført (Forventet)

15. juni 2020

Datoer for studieregistrering

Først innsendt

8. januar 2020

Først innsendt som oppfylte QC-kriteriene

8. januar 2020

Først lagt ut (Faktiske)

10. januar 2020

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

10. januar 2020

Siste oppdatering sendt inn som oppfylte QC-kriteriene

8. januar 2020

Sist bekreftet

1. januar 2020

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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