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Clinical Study to Evaluate the Pharmacokinetics and Safety of CKD-339 in Healthy Volunteers

31. juli 2026 oppdatert av: Chong Kun Dang Pharmaceutical

An Open Label, Randomized, Single Dose, Crossover, Phase I Study to Evaluate the Pharmacokinetics and the Safety of D311 and D107 Compared to CKD-339 in Healthy Adult Volunteers

This study is a randomized, open-label, single dose, crossover study to evaluate the pharmacokinetics and safety of CKD-339 in healthy volunteers.

Studieoversikt

Status

Har ikke rekruttert ennå

Forhold

Detaljert beskrivelse

To 76 healthy subjects, following treatments, are administered dosing in each period and wash-out period is 14 days.

Pharmacokinetic blood samples are collected up to 72hrs. The pharmacokinetic characteristics and safety are assessed.

Studietype

Intervensjonell

Registrering (Antatt)

76

Fase

  • Fase 1

Kontakter og plasseringer

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

Studiekontakt

Studiesteder

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

  • Voksen

Tar imot friske frivillige

Ja

Beskrivelse

Inclusion Criteria:

  1. Healthy adults between the age of 19 and 55 (inclusive) at the time of screening test.
  2. Subjects with a body mass index(BMI) between 18 and 30 kg/m2(BMI = Weight(kg)/ Height(m)2)

    • Male subjects weighing at least 50 kg
    • Female subjects weighing at least 45 kg
  3. Subjects who do not have clinically meaningful congenital or chronic diseases and who do not have medical examination results (such as electroencephalogram, electrocardiogram, chest and gastroscopy or gastrointestinal radiography, if necessary) during screening visits.
  4. Subjects judged by investigators to be suitable for screening tests based on laboratory tests (e.g., blood tests, urine tests) and ECG, which were conducted according to the characteristics of the IP.
  5. Subjects who voluntarily signed and dated the informed consent form after fully understanding its contents.
  6. Subjects who had agreed to use medically appropriate contraceptive methods* to exclude the possibility of pregnancy from the first dose of the IP to 14 days after the last dose, and not to donate sperm or ovum.

    • contraceptive methods: Combination use of intrauterine device (IUD) or system (IUS), vasectomy, tubal ligation, tubal occlusion and barrier methods of contraception (male condoms, female condoms, cervical caps, contraceptive diaphragm, sponges, etc.) or the use of combined spermicide, involves the simultaneous use of two or more barrier methods.

Exclusion Criteria:

  1. Subjects who have taken a drug metabolase-inducing and inhibiting drug such as barbitals within one month prior to the first dosing date or a drug that may interfere with this test within 10 days prior to the first dose of IP.
  2. Subjects who had been administered investigational product from other clinical study or bioequivalence study within the 6 months prior to the first dose of IP.
  3. Subjects who donated whole blood within 8 weeks, or blood components within 2 weeks prior to the first dose of IP.
  4. Subjects who have a history of gastrointestinal resection that may affect the absorption of drugs.
  5. Subjects with a history of regular alcohol consumption meeting any of the following criteria within 1 month prior to the first dose of IP.

    • Man: average alcohol consumption > 21 cups/weeks
    • Woman: average alcohol consumption > 14 cups/weeks
  6. Patients with the following conditions

    • Patients who have a history of hypersensitivity to main or component of clinical trial drugs and other dihydropyridine drugs
    • Patients on angiotensin converting enzyme (ACE) inhibitor or not more than 36 hours after discontinuation of administration
    • Patients with a history of angiotensin converting enzyme (ACE) inhibitors or angiotensin receptor antagonists (ARB) administration
    • Patients with hereditary or idiopathic angioedema
    • Patients with severe liver failure, cirrhosis or biliary obstruction, bile congestion
    • Patients with diabetes or moderate to severe renal impairment (eGFR < 60mL/min/1.73m2) who have been co-administered with alliskyrene
    • Patients with primary aldosteronism
    • Shock patients (including cardiac shock)
    • Patients with severe aortic valve stenosis
    • Patients with unstable angina
    • Patients within one month of the onset of myocardial infarction
  7. Subjects with a history of psychiatric disorders.
  8. Subjects who are considered unsuitable for participation in this bioequivalence study by the Investigator (or delegated Sub-investigator) for reasons other than the inclusion and exclusion criteria listed above.
  9. Female subjects who are pregnant, suspected of being pregnant, or breastfeeding.

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: Sequence A(Reference-Test)
Period 1: A single oral dose of 2 tablets under fasting condition(D311, D107), Period 2: A single oral dose of 1 tablet under fasting condition(CKD-339)
QD, PO
Andre navn:
  • Test
QD, PO
Andre navn:
  • Henvisning
Eksperimentell: Sequence B(Test-Reference)
Period 1: A single oral dose of 1 tablet under fasting condition(CKD-339), Period 2: A single oral dose of 2 tablets under fasting condition(D311, D107)
QD, PO
Andre navn:
  • Test
QD, PO
Andre navn:
  • Henvisning

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
AUCt of CKD-339
Tidsramme: From 0 to 72 hours postdose
Area under the plasma CKD-339 concentration-time curve from 0 to t
From 0 to 72 hours postdose
Cmax of CKD-339
Tidsramme: From 0 to 72 hours postdose
The maximum concentration of CKD-339 in plasma
From 0 to 72 hours postdose

Samarbeidspartnere og etterforskere

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

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 (Antatt)

20. august 2026

Primær fullføring (Antatt)

6. oktober 2026

Studiet fullført (Antatt)

12. oktober 2026

Datoer for studieregistrering

Først innsendt

28. juli 2026

Først innsendt som oppfylte QC-kriteriene

31. juli 2026

Først lagt ut (Faktiske)

6. august 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

6. august 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

31. juli 2026

Sist bekreftet

1. juli 2026

Mer informasjon

Begreper knyttet til denne studien

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • A164_01BE2511

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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