- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT05019755
A Study to Investigate the Effect of Food on the Pharmacokinetics of IN-A002 Capsule in Healthy Male Subjects
A Randomized, Open-label, Single-dose, 2-way Crossover Clinical Trial to Investigate the Effect of Food on the Pharmacokinetics of IN-A002 Capsule in Healthy Male Subjects
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
Studietyp
Inskrivning (Förväntat)
Fas
- Fas 1
Kontakter och platser
Studiekontakt
- Namn: Sohyun Kim, BS
- Telefonnummer: +82-2-6477-0225
- E-post: sohyun.kim21@inno-n.com
Studieorter
-
-
-
Seoul, Korea, Republiken av
- Rekrytering
- Seoul National University Hospital, Dept. of Clinical Pharmacology
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
- Healthy male adults aged 19 to 55 years (inclusive) at the time of signing the informed consent form.
- Body mass index (BMI) ≥ 18.0 and ≤ 30.0 kg/m^2 with a body weight ≥ 50.0 kg and ≤ 90.0 kg at screening. BMI (kg/m^2) = Weight(kg) / {Height(m)}^2
- Decides to participate voluntarily in the study after being fully informed of and understanding the study completely, and provides his written informed consent prior to screening procedure.
- Determined eligible for this study in the opinion of the investigator based on the results of vital signs, physical examination, 12-lead electrocardiogram, clinical laboratory tests, and medical interview.
Exclusion Criteria:
- Has a history or current evidence of clinically significant disorder of hepatic, renal, nervous, respiratory, endocrine, hemato-oncologic, cardiovascular, urinary, and/or psychiatric system.
- Has a history or current evidence of gastrointestinal disease that may affect the safety and Pharmacokinetics assessment of investigational product(IP) or a history of gastrointestinal surgery (except for simple appendectomy or herniotomy).
- Has rheumatoid arthritis or has a history.
- Has symptomatic herpes simplex or herpes zoster or has a history within 3 months prior to the scheduled first dose.
- Has live vaccine dose within 3 months prior to the scheduled first dose or expects to receive live vaccine during the clinical trial period.
- Has a history or current evidence of clinically significant hypersensitivity to drugs containing any ingredient of Janus kinase inhibitor and other drugs.
- Has a positive result on serology tests (for hepatitis B, hepatitis C and human immunodeficiency virus [HIV], syphilis) during screening test.
- Has abnormalities one or more of the following during screening test: AST [GOT] or ALT [GPT] > 1.5 X upper limit of normal (ULN), Creatinine > upper limit of normal (ULN), ANC < 2,000/uL, Hb < 12.5 g/dL, Platelet < 150,000/uL, QTc interval at 12-lead electrocardiogram > 450 msec
- Systolic blood pressure (SBP) < 90 mmHg or > 140 mmHg, diastolic blood pressure (DBP) < 50 mmHg or > 95 mm Hg, or pulse rate (PR) < 45 beats/ min or > 100 beats/min on vital signs measured in sitting position after taking a rest for at least 5 minutes during screening test.
- Has a history of drug abuse or has a positive response to drug abuse on urine drug screening test.
- Has taken any prescription drugs or herbal medicine within 2 weeks prior to the expected date of first dose, or any over-the-counter (OTC) drug, health functional food or vitamin preparation within 1 week prior to the scheduled first dose (However, can participate in the study if otherwise eligible in the judgment of the investigator) or is expected to take such medication during the study.
- Has participated in any other clinical study, etc. and received IPs within 6 months prior to the scheduled first dose.
- 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.
- Has a history of excessive smoking (> 10 cigarettes/day) within 3 months prior to the scheduled first dose or confirmed as positive for cotinine on urine drug screening test.
- Excessive caffeine intake (> 5 units/day) or continued use of alcohol (> 21 units/week, 1 unit = 10 g of pure alcohol).
- Unable to stop drinking within 24 hrs prior to the scheduled first dose to post study visit.
- Unable to avoid caffeine-containing foods (e.g., coffee, tea [black tea, green tea, etc.], soda, coffee-flavored milk, and nutritive tonic drink, etc.) and foods containing grapefruit during each period from 24 hrs before hospitalization to discharge.
Unable to use a medically acceptable contraceptive method stated below and does not agree not to donate sperm from the scheduled first dose to 90 days after the last dose.
- Use of intrauterine device with a proven birth control failure rate by the spouse (or partner)
- Simultaneous use of (male or female) barrier method and spermicide
- Surgical sterilization of the subject or his partner (e.g., vasectomy, salpingectomy, tubal ligation, or hysterectomy)
- Determined ineligible for study participation by the investigator for other reasons.
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Crossover tilldelning
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
---|---|
Experimentell: A(First period) to B(Second period) order
A: Oral Administration of IN-A002(IN-115314) in fasting status B: Oral Administration of IN-A002(IN-115314), 30 minutes after high-fat diet There will be a wash out period of 7days between period |
Oral Administration of IN-A002(IN-115314), single dose
|
Experimentell: B(First period) to A(Second period) order
B: Oral Administration of IN-A002(IN-115314), 30 minutes after high-fat diet A: Oral Administration of IN-A002(IN-115314) in fasting status There will be a wash out period of 7days between period |
Oral Administration of IN-A002(IN-115314), single dose
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
---|---|
Cmax of IN-A002(IN-115314)
Tidsram: up to 72 hours
|
up to 72 hours
|
AUClast of IN-A002(IN-115314)
Tidsram: up to 72 hours
|
up to 72 hours
|
Sekundära resultatmått
Resultatmått |
Tidsram |
---|---|
AUCinf of IN-A002(IN-115314)
Tidsram: up to 72 hours
|
up to 72 hours
|
Tmax of IN-A002(IN-115314)
Tidsram: up to 72 hours
|
up to 72 hours
|
t1/2 of IN-A002(IN-115314)
Tidsram: up to 72 hours
|
up to 72 hours
|
λz of IN-A002(IN-115314)
Tidsram: up to 72 hours
|
up to 72 hours
|
CL/F of IN-A002(IN-115314)
Tidsram: up to 72 hours
|
up to 72 hours
|
Vd/F of IN-A002(IN-115314)
Tidsram: up to 72 hours
|
up to 72 hours
|
Cmax of IN-116118(primary metabolite of IN-A002(IN-115314))
Tidsram: up to 72 hours
|
up to 72 hours
|
AUClast of IN-116118(primary metabolite of IN-A002(IN-115314))
Tidsram: up to 72 hours
|
up to 72 hours
|
AUCinf of IN-116118(primary metabolite of IN-A002(IN-115314))
Tidsram: up to 72 hours
|
up to 72 hours
|
Tmax of IN-116118(primary metabolite of IN-A002(IN-115314))
Tidsram: up to 72 hours
|
up to 72 hours
|
t1/2 of IN-116118(primary metabolite of IN-A002(IN-115314))
Tidsram: up to 72 hours
|
up to 72 hours
|
λz of IN-116118(primary metabolite of IN-A002(IN-115314))
Tidsram: up to 72 hours
|
up to 72 hours
|
Metabolite ratio of IN-116118(primary metabolite of IN-A002(IN-115314))
Tidsram: up to 72 hours
|
up to 72 hours
|
Samarbetspartners och utredare
Sponsor
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Förväntat)
Avslutad studie (Förväntat)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- IN_JSI_103
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Studerar en amerikansk FDA-reglerad produktprodukt
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .
Kliniska prövningar på Friska
-
University of MiamiJames and Esther King Biomedical Research ProgramAvslutadHealthy Lifetime Icke-rökareFörenta staterna
-
University of LeicesterNational Institute for Health Research, United KingdomAvslutadPatienter med hjärtsvikt och konserverad ejektionsfraktion - HFpEF | Patienter med hjärtsvikt med reducerad ejektionsfraktion - HFrEF | Healthy Controls Group - ålders- och könsmatchad
-
University Hospital, GrenobleUniversity Hospital, Clermont-Ferrand; Grenoble Institut des NeurosciencesAvslutadParkinsons sjukdom | Healthy Controls Group - ålders- och könsmatchadFrankrike
Kliniska prövningar på IN-A002(IN-115314) capsule
-
HK inno.N CorporationHar inte rekryterat ännu
-
HK inno.N CorporationOkänd
-
HK inno.N CorporationAvslutadParenteral näringKorea, Republiken av
-
Duke UniversityEunice Kennedy Shriver National Institute of Child Health and Human Development... och andra samarbetspartnersRekrytering
-
IVI VigoInstituto Valenciano de Infertilidad, IVI VALENCIAAvslutad
-
BlueWillow BiologicsPorton Biopharma Ltd.Avslutad
-
Starkey Laboratories, IncAvslutadHörselnedsättning | Hörselnedsättning, sensorineuralFörenta staterna
-
HK inno.N CorporationAvslutadFriskaKorea, Republiken av
-
Abbott Point of CareAvslutadAnalytisk prestanda för natrium-, glukos- och hematokritanalyser av i-STAT 500 (Alinity) analysatorFörenta staterna