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To Evaluate the Safety, Tolerability, Pharmacokinetics and the Effect of Food on the Hemay5259 Sustained-release Tablets in Healthy Subjects.

9. juli 2026 opdateret af: Hemay Pharmaceutical PTY. LTD.

A Randomized, Double-blind, Placebo-controlled, Single and Multiple Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Food Effect of Hemay5259 Extended-Release Tablet in Healthy Participants

Evaluation of the pharmacokinetics of Hemay 5259 sustained-release tablets in healthy human subjects

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

32

Fase

  • Fase 1

Kontakter og lokationer

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

Studiekontakt

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

  • Voksen

Tager imod sunde frivillige

Ja

Beskrivelse

Inclusion Criteria:

  • Must have given written informed consent before any study-related activities are carried out and must be able to understand the full nature and purpose of the study, including possible risks and adverse effects.
  • Adult males and females between ≥ 18 and ≤ 55 years (inclusive) at Screening.
  • Body mass index (BMI) ≥ 18.0 and ≤ 30.0 kg/m2 with a body weight ≥ 50 kg (males) or ≥45 kg (females) at Screening.
  • Participants with normal results or non-clinically significant (NCS) abnormal results in the opinion of the PI or delegate for a comprehensive examination, including physical examination, vital signs examination, laboratory tests (hematology, biochemistry, coagulation and urinalysis).
  • a)Female participants are eligible to participate if they are not pregnant, not breastfeeding, and at least 1 of the following conditions applies:

    • Women of non-childbearing potential (WONCBP), defined as surgically sterile (hysterectomy, bilateral salpingectomy, or bilateral oophorectomy - verbal confirmation through medical history review acceptable) or postmenopausal (no menses for 12 months and confirmed by follicle stimulating hormone [FSH] level >40 mIU/mL);
    • Woman of childbearing potential (WOCBP) and agree to practice true abstinence or agrees to use an highly effective method of contraception (refer to Section 4.6.3) consistently from the signing of informed consent form (ICF) to 90 days after the last dose of IPs and refrain from donating eggs during this period. And WOCBP must have a negative serum pregnancy test at screening and a negative urine pregnancy test at Day -1.
    • Participant is in an exclusively same-sex relationship. b)Male participants must agree to practice true abstinence; be surgically sterilized (performed at least 6 months prior to screening and documented to no longer produce sperm - verbal confirmation through medical history review acceptable); or agree to use a condom plus effective contraception methods (refer to Section 4.6.3) for their female partner, if of childbearing potential, from the signing of ICF to 90 days after the last dose of IPs and refrain from donating sperm during this period. These contraception requirements do not apply if the male participant is in an exclusively same sex relationship.
  • Able and willing to attend the necessary visits to the study site. Exclusion Criteria:
  • Any history or presence of clinically relevant cardiovascular, pulmonary, gastrointestinal, hepatic, renal, metabolic, hematological, neurological, musculoskeletal, rheumatological, psychiatric , systemic, ocular, or infectious disease, or signs of acute illness.
  • Any history or presence of depression.
  • Any history or presence of gastrointestinal, hepatic, renal disease that affect drug absorption or metabolism.
  • Any surgery within 1 months prior to the first dose.
  • Any history or presence of chronic infectious diseases such as tuberculosis (judged by the Investigator according to QuantiFERON gold).
  • Participants with a clinically significant infection history within 4 weeks prior to first dose, or any serious infection requiring intravenous antimicrobial therapy within 6 months prior to Screening.
  • Alkaline phosphatase (ALP), aspartate aminotransferase (AST), and alanine aminotransferase (ALT) >1.5 × upper limit of normal (ULN) at Screening or Day -1.
  • Participants with clinically significant abnormal 12-lead electrocardiogram (ECG) results as judged by the PI or delegate or with a corrected QTc (formula: QTcF = QT/RR1/3) interval greater than 450 msec in males and 470 msec in females.
  • Participants with positive test results for hepatitis B surface antigen (HBsAg), hepatitis C virus antibody (HCV Ab), treponema pallidum antibody (Syphilis TP Ab) or human immunodeficiency virus antibody (HIV Ab) at Screening.
  • Participants with estimated glomerular filtration rate (eGFR) < 90 mL/min/1.73m2 (using the CKD-EPI equation).
  • Presence or history of drug/food hypersensitivity, or anaphylactic reaction, diagnosed and treated by a physician, or have special dietary requirements.
  • Known hypersensitivity to any component of the IP formulation.
  • Participants who regularly drink more than 14 standard units of alcohol per week for females and more than 21 standard units of alcohol per week for males; 1 standard unit contains 10 g of alcohol, such as 285 mL of beer, 30 mL of 40% spirits or 100 mL of wine within 6 months prior to Screening.
  • Participants with a history of drug abuse or a positive drug abuse screening test.
  • Regular smoking (defined as more than 5 cigarettes or equivalent per week) within one year prior to the first dose, or unable to stop smoking from 48 hours prior to the first drug administration to the last time point for collecting PK blood samples.
  • Positive alcohol test at screening and check-in on D-1.
  • Any consumption of xanthine bases and/or grapefruit or products containing xanthine bases and/or grapefruit within 2 weeks prior to the first dose; or unable to stop consumption of above ingredients from first drug administration to the last time point for collecting PK blood samples.
  • Any consumption of chocolate or caffeine or products containing caffeine within 48 h prior to the first dose; or unable to stop consumption of above ingredients from first drug administration to the last time point for collecting PK blood samples.
  • Any consumption of alcohol or products containing alcohol within 48 h prior to Day-1; or unable to stop consumption of alcohol first drug administration to the last time point for collecting PK blood samples.
  • Any drug that inhibits or induces liver drug metabolism (inducers include barbiturates, carbamazepine, rifampicin, phenytoin, glucocorticoids, omeprazole, etc.; inhibitors include selective serotonin reuptake inhibitor (SSRI) antidepressants, cimetidine, diltiazem, macrolides, nitroimidazoles, sedative-hypnotics, verapamil, fluoroquinolones, antihistamines, etc.) within 30 days prior to the first dose or during the study.
  • Any prescription medication, within 14 days prior to administration of the first dose or within 5 times the elimination t1/2 of the medication, with the exception of hormonal contraception, menopausal hormone replacement therapy or occasional analgesics such as Paracetamol, Ibuprofen and standard daily vitamins etc. in short term at the Investigator's direction.
  • Made a blood donation > 400 ml within 4 weeks prior to the first dose or during the study or planning to donate blood during the study and follow up period.
  • Any participant who enrolled in or participated in any other clinical study involving an IP, or in any other type of medical research within 1 month or within 5 times the elimination t1/2 prior to administration of the first dose.
  • Any vaccination in the 14 days prior to administration of the first dose.
  • Any participant in whom venous blood collection is difficult.
  • Any participant who, in the judgment of the Investigator, is likely to be non-compliant during the study, or to be unable to cooperate due to language problems or poor mental development.
  • Any participant who is the Investigator or any subinvestigator, research assistant, pharmacist, study coordinator, or other staff thereof directly involved in conducting the study or any person dependent on (employees or immediate family members) the study site, the Investigator or the Sponsor.

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: Parallel tildeling
  • Maskning: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Hemay5259 group 1
Part1: Food effect group Hemay005 extended-release will be taken orally in single dose with a high-fat, high-calorie meal or at overnight fasting. Part 2: Multiple doses group Hemay005 extended-release will be taken orally once daily in 120mg
Food influence test: single administration of the drug, multiple dosing trial: administration once daily
Placebo komparator: Placebo group 1
Part1: Food effect group Hemay005 extended-release will be taken orally in single dose with a high-fat, high-calorie meal or at overnight fasting. Part 2: Multiple doses group Hemay005 extended-release will be taken orally once daily.
Food effect trial: single administration of the drug, multiple dosing trial: administration once daily
Eksperimentel: Hemay5259 group 2
Part1: Food effect group Hemay005 extended-release will be taken orally in single dose with a high-fat, high-calorie meal or at overnight fasting. Part 2: Multiple doses group Hemay005 extended-release will be taken orally once daily in 150mg
Food influence test: single administration of the drug, multiple dosing test: administration once daily
Placebo komparator: Placebo group 2
Part1: Food effect group Hemay005 extended-release will be taken orally in single dose with a high-fat, high-calorie meal or at overnight fasting. Part 2: Multiple doses group Hemay005 extended-release will be taken orally once daily.
Food influence test: single administration of the drug, multiple dosing test: administration once daily

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Pharmacokinetics (PK) of Hemay5259: Maximum plasma concentration (Cmax)in Part 1 and Part 2
Tidsramme: Day1-Day4,Day10-Day22
Day1-Day4,Day10-Day22
Pharmacokinetics (PK) of Hemay5259: Area under the curve from time 0 to the last measurable concentration (AUC0-last) in single dose and Multiple dose
Tidsramme: Day1-Day4,Day10-Day22
Day1-Day4,Day10-Day22
Pharmacokinetics (PK) of Hemay5259: Area under the curve from time 0 extrapolated to infinite time (AUC0-inf)single dose and Multiple dose
Tidsramme: Day1-Day4,Day10-Day22
Day1-Day4,Day10-Day22
Pharmacokinetics (PK) of Hemay5259:time to Cmax (Tmax) in single dose and Multiple dose
Tidsramme: Day1-Day4,Day10-Day22
Day1-Day4,Day10-Day22
Pharmacokinetics (PK) of Hemay5259:time to half-life (t1/2)in single dose and Multiple dose
Tidsramme: Day1-Day4,Day10-Day22
Day1-Day4,Day10-Day22
PK of Hemay5259: Observed Apparent volume of distribution (Vz/F) in singel dose and multiple dose:
Tidsramme: Day1-Day4,Day10-Day22
Day1-Day4,Day10-Day22
PK of Hemay5259: Observed Accumulation ratio calculated from AUC (Rac(AUC)) in multiple dose
Tidsramme: D13-D22
D13-D22
PK of Hemay5259: Observed Accumulation ratio calculated from Cmax (Rac(Cmax)) in multiple dose
Tidsramme: Day13-Day22
Day13-Day22

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Adverse events assessments after single and multiple ascending dose administration at baseline and repeatedly until study completion
Tidsramme: through study completion, an average of 1 month
This safety outcome combines the measure of the number of subjects experiencing adverse events (AEs), the nature and severity of those AEs and their relationship to the study treatments.
through study completion, an average of 1 month

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 (Anslået)

1. juli 2026

Primær færdiggørelse (Anslået)

31. august 2026

Studieafslutning (Anslået)

31. oktober 2026

Datoer for studieregistrering

Først indsendt

18. juni 2026

Først indsendt, der opfyldte QC-kriterier

9. juli 2026

Først opslået (Faktiske)

15. juli 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

15. juli 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

9. juli 2026

Sidst verificeret

1. juli 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • HM5259HV1S01

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Studerer et amerikansk FDA-reguleret enhedsprodukt

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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 .

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