Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

Study of Single and Multiple Oral Doses of SCB0020160 in Healthy Adult Male Subjects

26. juni 2026 oppdatert av: SCBIO Inc.

A First-in-Human, Double-blind, Placebo-controlled, Single and Multiple Ascending Dose, Phase 1 Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Food Effect of SCB0020160 After Oral Administration in Healthy Adult Male Subjects

This study aims to evaluate the safety, tolerability, pharmacokinetics, and food effect of a new investigational medicine called SCB0020160 in healthy adult men. This is the first time SCB0020160 will be administered to humans.

Healthy adult men aged 18 to 65 years who meet the study eligibility criteria.

Study details

Participants will be randomly assigned to receive either SCB0020160 or placebo. The study includes single-dose and multiple-dose treatment periods, as well as an assessment of the effect of food on the absorption of SCB0020160.

Participants will undergo safety assessments including physical examinations, vital signs, ECGs, blood and urine tests, and monitoring of adverse events. The study will also assess how SCB0020160 is processed by the body.

There is no direct health benefit expected from participation. The results may help determine safe dose levels and support future clinical development of SCB0020160.

Studieoversikt

Status

Har ikke rekruttert ennå

Detaljert beskrivelse

This study evaluates the safety, tolerability, and pharmacokinetics of SCB0020160 or placebo following single and multiple oral doses in healthy adult male subjects. A total of 74 subjects were planned, including 64 target subjects (8 per dose group) and 10 substitute subjects. The study may be completed without enrolling substitute subjects if all 64 target subjects complete the study.

Studietype

Intervensjonell

Registrering (Antatt)

74

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

    • South Australia
      • Adelaide, South Australia, Australia, 5000
        • CMAX Clinical Research Pty Ltd Ground Floor, 21-24 North Terrace

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
  • Eldre voksen

Tar imot friske frivillige

Ja

Beskrivelse

Inclusion Criteria:

  • Healthy adult male volunteers in the opinion of the principal investigator or delegate, aged 18 to 65 years at screening
  • Body weight more Than or equals to 45.0 kilograms per square meter at screening, with a body mass index (BMI) of more than or equals to18.0-kilogram Meter square and less than or equals to 32.0 Kilograms per meter square

    • Body Mass Index (BMI, kilograms per square meter.) = Weight (kilogram)/[Height square meter]
  • Eligible to participate in the study based on the results of physical examination, clinical laboratory tests, history taking, and other examinations performed at screening, as determined by the principal investigator or delegate
  • Has voluntarily decided to participate and provided written or electronic consent to comply with the precautions after receiving a full explanation of the study and fully understanding it

Exclusion Criteria:

  • Has a history of or currently has any disease, including clinically significant hepatobiliary (severe liver impairment, viral hepatitis, etc.), renal (severe renal impairment, etc.), neurological, immunological, respiratory, digestive, endocrine, hematologic and oncologic, cardiovascular (Torsades de pointes, etc.), urological, psychiatric (mood disorders, obsessive compulsive disorder, etc.), and sexual function disorders
  • Has a history of or currently has a gastrointestinal disease (Crohn's disease, ulcerative colitis, etc.) that may affect the safety and pharmacokinetic evaluation of the investigational product, or has a history of gastrointestinal surgery (except for simple appendectomy or hernia surgery)
  • Has a history of hypersensitivity to the active pharmaceutical ingredient and components of the investigational product, drugs in the same class as the active pharmaceutical ingredient, or other drugs (aspirin, antibiotics, etc.)
  • Has genetic problems such as galactose intolerance, Lapp lactase deficiency, or glucose galactose malabsorption
  • Has any of the following results in vital signs measured in a sitting position after resting for at least 5 minutes at screening
  • Systolic blood pressure more than 80 millimeters of mercury or greater than or equal to140 mmHg
  • Diastolic blood pressure less than 45 millimeters of mercury or greater than or equal to140 mmHg 90 millimeters of mercury
  • Pulse rate less than 45 beats/min or > 105 beats/min
  • Has any of the following results in the 12-lead electrocardiogram measured in a semi-supine position after resting for at least 5 minutes at screening, or has clinically significant rhythm findings
  • QTcF less than 450 msec
  • Has any of the following results in the screening clinical laboratory tests
  • Estimated Glomerular Filtration Rate (eGFR) (CKD-EPI equation) < 90 mL/min/1.73 m²
  • Fasting serum glucose more than 5.4 millimoles per liter. or less than 3.0 millimoles per liter.
  • AST or ALT 1.5 X the upper limit of normal (ULN)
  • Total cholesterol less than 5.5 millimoles per liter
  • Triglyceride less than 2.0 millimoles per liter.
  • Drinks alcohol persistently (less than 21 units/week, 1 unit = 10 gram = 12.5 milli liter of pure alcohol) or is unable to refrain from alcohol consumption from 3 days prior to the expected first dose of the investigational product until the end of the study
  • Tested positive for the breath alcohol test at screening or at check-in on D-1 10) Smokers (However, those who quit smoking 3 months prior to the expected first dose of the investigational product may be eligible as subjects)
  • Tested positive for the urine cotinine test at screening or at check-in on D-1, even if they do not smoke
  • Has taken any prescribed drugs or herbal medicines within 2 weeks prior to the expected first dose, or has taken any over-the-counter (OTC) drugs, health functional foods including liver supplements, or vitamins within 1 week (However, they may participate in the study if the investigator deems their other conditions appropriate), or is expected to take any of the said agents
  • Has taken drugs that induce drug-metabolizing enzymes, such as barbiturates, or drugs that inhibit drug metabolism, such as clarithromycin, within 1 month prior to the expected first dose
  • Has a history of alcohol or drug abuse, or has shown a positive result for abused drugs in a urine drug test at screening or at check-in on D-1
  • Has participated in another study (including bioequivalence studies) and received an investigational product within 3 months prior to the first dose
  • Has donated whole blood within 2 months, donated blood components within 1 month, or received a blood transfusion within 1 month prior to the expected first dose
  • Has persistently consumed excessive amounts of caffeine (> 5 units/day, 1 unit = 80 mg of caffeine), or is unable to refrain from consuming caffeine-containing foods (coffee, tea (black tea, green tea, etc.), carbonated beverages, coffee-flavored milk, health tonics, energy drinks, etc.) from 3 days prior to the expected first dose of the investigational product until the end of the study
  • Has consumed grapefruit, grapefruit juice, or grapefruit-containing foods from 3 days prior to the expected first dose of the investigational product until the end of the study, or is unable to refrain from consuming grapefruit-containing foods during this period
  • Has unusual eating habits (e.g., consuming more than 1L of grapefruit juice per day) or is unable to consume the standard diet provided by the study site during the inpatient period
  • Tested positive for serological tests (hepatitis B test, hepatitis C test, human immunodeficiency virus (HIV) test, syphilis test)
  • Subjects who, or whose spouse (or partner) is a woman of childbearing potential, are unable or unwilling to use methods of contraception considered highly effective for the entire period of the study and for at least 90 days after the last dose of the investigational product, and who do not agree to avoid donating sperm/eggs during this period.

[Methods of contraception considered highly effective]

  • Intrauterine devices and intrauterine hormone-releasing systems with a proven contraception failure rate (< 1%/year) plus the use of a male condom
  • Bilateral tubal occlusion or bilateral tubal ligation plus the use of a male condom
  • Azoospermia is confirmed by sperm test after vasectomy
  • Hormonal contraception (e.g., combined oral contraceptive, progestogen-only oral contraceptive), contraceptive patch, vaginal ring, injection, subdermal contraceptive implant); however, hormonal contraception is limited to cases where it is being used for 28 days or longer prior to the administration of the investigational product and can be continuously used during the study period and up to 90 days after the last dose plus the use of a male condom.
  • Sexual abstinence, if it is the usual and preferred method of contraception.
  • Those judged by the principal investigator or delegate to be ineligible for participation in the study for reasons other than the above-mentioned criteria (non-compliance with instructions, etc.)

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: Parallell tildeling
  • Masking: Trippel

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: SCB0020160
Single and multiple oral doses of SCB0020160
Single and multiple oral doses of SCB0020160 administered under fasting conditions. A food-effect evaluation following a single oral dose will be conducted in Part A Cohort 4.
Placebo komparator: Placebo
Matching placebo administered under the same dosing conditions
Matching placebo administered orally under the same dosing conditions as SCB0020160, including participation in the food-effect evaluation in Part A Cohort 4

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Incidence and frequency of adverse events, adverse drug reactions, serious adverse events, and serious adverse drug reactions
Tidsramme: From first dose through Post-Study Visit (up to Day 33)
Adverse event analysis will be conducted on Treatment Emergent Adverse Events (TEAEs)
From first dose through Post-Study Visit (up to Day 33)
For Physical examination to evaluate General Appearance
Tidsramme: From first dose through Post-Study Visit (up to Day 33)

For General Appearance assessments are:

Level of consciousness (alert, oriented) Nutritional status (well/poorly nourished) Build and posture Signs of distress (pain, dyspnea, fatigue) Hygiene and grooming

From first dose through Post-Study Visit (up to Day 33)
For Physical examination to evaluate HEENT
Tidsramme: From first dose through Post-Study Visit (up to Day 33)

For HEENT assessments are:

Head: shape, scalp lesions Eyes: pupil size/reactivity (PERRLA), vision, conjunctiva (pallor/icterus) Ears: hearing, discharge Nose: obstruction, discharge Throat: oral mucosa, tonsils, pharynx

From first dose through Post-Study Visit (up to Day 33)
For Physical examination to evaluate Neck (incl Thyroid & Nodes)
Tidsramme: From first dose through Post-Study Visit (up to Day 33)
for Neck (incl Thyroid & Nodes) assessment are: Thyroid size, nodules, tenderness Cervical lymphadenopathy Neck mobility Jugular venous pressure (if relevant
From first dose through Post-Study Visit (up to Day 33)
For Physical examination to evaluate Cardiovascular
Tidsramme: From first dose through Post-Study Visit (up to Day 33)

For Cardiovascular assessment are:

Heart rate and rhythm Heart sounds (S1, S2, murmurs) Peripheral pulses Edema (peripheral) Blood pressure

From first dose through Post-Study Visit (up to Day 33)
For Physical examination to evaluate Respiratory
Tidsramme: From first dose through Post-Study Visit (up to Day 33)

For Respiratory assessment are:

Respiratory rate and effort Chest expansion symmetry Breath sounds (normal, wheeze, crackles) Use of accessory muscles

From first dose through Post-Study Visit (up to Day 33)
For Physical examination to evaluate Gastrointestinal
Tidsramme: From first dose through Post-Study Visit (up to Day 33)

For Gastrointestinal assessment are:

Abdominal inspection (distension, scars) Palpation (tenderness, masses, organomegaly) Percussion (fluid, liver span) Bowel sounds

From first dose through Post-Study Visit (up to Day 33)
For Physical examination to evaluate Renal
Tidsramme: From first dose through Post-Study Visit (up to Day 33)

For Renal assessment are:

Flank tenderness (costovertebral angle) Bladder distension Urinary symptoms

From first dose through Post-Study Visit (up to Day 33)
For Physical examination to evaluate Neurological
Tidsramme: From first dose through Post-Study Visit (up to Day 33)

For Neurological assessment are:

Mental status (orientation, cognition) Cranial nerves (if detailed exam required) Motor function (strength, tone) Sensory function Reflexes Coordination and gait

From first dose through Post-Study Visit (up to Day 33)
For Physical examination to evaluate Musculoskeletal
Tidsramme: From first dose through Post-Study Visit (up to Day 33)

For Musculoskeletal assessment are:

Joint range of motion Swelling or deformities Muscle strength Tenderness

From first dose through Post-Study Visit (up to Day 33)
For Physical examination to evaluate Skin
Tidsramme: From first dose through Post-Study Visit (up to Day 33)

For Skin assessment are:

Color (pallor, cyanosis, jaundice) Rashes or lesions Texture and turgor Ulcers or scars

From first dose through Post-Study Visit (up to Day 33)
For Vital signs (body temperature (tympanic)
Tidsramme: From first dose through Post-Study Visit (up to Day 33)
For body temperature (tympanic) the measurement of unit is degree Celsius
From first dose through Post-Study Visit (up to Day 33)
For Vital signs (Pulse Rate)
Tidsramme: From first dose through Post-Study Visit (up to Day 33)
For Pulse Rate the measurement of unit is - beats/min
From first dose through Post-Study Visit (up to Day 33)
For Vital signs (Systolic/Diastolic blood pressure)
Tidsramme: From first dose through Post-Study Visit (up to Day 33)
For Systolic/Diastolic blood pressure the measurement of unit is - mmHg
From first dose through Post-Study Visit (up to Day 33)
For 12-lead ECG (electrocardiogram)
Tidsramme: From first dose through Post-Study Visit (up to Day 33)
The investigator evaluates heart rate (rate and regularity), waveform shape, and overall rhythm; QTcF (msec) is used in the screening criteria will be collectively assessed
From first dose through Post-Study Visit (up to Day 33)
For Clinical Laboratory Test which includes Urinalysis
Tidsramme: From first dose through Post-Study Visit (up to Day 33)
For Urinalysis - Dipstick + microscopy
From first dose through Post-Study Visit (up to Day 33)
For Clinical Laboratory Test which includes the Coagulation
Tidsramme: From first dose through Post-Study Visit (up to Day 33)
For Coagulation - Prothrombin Time (PT) (INR), Activated Partial Thromboplastin Time (aPTT)
From first dose through Post-Study Visit (up to Day 33)
For Clinical Laboratory Test which includes the Blood chemistry
Tidsramme: From first dose through Post-Study Visit (up to Day 33)
For Blood chemistry the test performed will be Calcium, phosphate, glucose, urate, cholesterol, total protein, albumin, total bilirubin, Alkaline Phosphatase (ALP), Aspartate Aminotransferase (AST), Alanine Aminotransferase (ALT), Gamma-Glutamyl Transferase (γ-GT), Creatine Phosphokinase (CPK), Urea, Lactate Dehydrogenase (LDH), creatinine, Estimated Glomerular Filtration Rate (eGFR) (CKD-EPI), sodium, potassium, chloride, triglyceride, Low-Density Lipoprotein Cholesterol (LDL) & High-Density Lipoprotein Cholesterol (HDL)
From first dose through Post-Study Visit (up to Day 33)
For Clinical Laboratory Test which includes the Hematology
Tidsramme: From first dose through Post-Study Visit (up to Day 33)
For Hematology the test performed will be white blood cells with differential, Red blood cells, hemoglobin, hematocrit & platelet
From first dose through Post-Study Visit (up to Day 33)
Pharmacokinetic Parameters of SCB0020160 for Cmax
Tidsramme: Up to Day 8 (Part A), Up to Day 21 (Part B), and Up to Day 29 for the Food Effect Cohort
The results of the outcome are collectively measured
Up to Day 8 (Part A), Up to Day 21 (Part B), and Up to Day 29 for the Food Effect Cohort
Pharmacokinetic Parameters of SCB0020160 for Tmax
Tidsramme: Up to Day 8 (Part A), Up to Day 21 (Part B), and Up to Day 29 for the Food Effect Cohort
The results of the outcome are collectively measured
Up to Day 8 (Part A), Up to Day 21 (Part B), and Up to Day 29 for the Food Effect Cohort
Pharmacokinetic Parameters of SCB0020160 for AUClast
Tidsramme: Up to Day 8 (Part A), Up to Day 21 (Part B), and Up to Day 29 for the Food Effect Cohort
The results of the outcome are collectively measured
Up to Day 8 (Part A), Up to Day 21 (Part B), and Up to Day 29 for the Food Effect Cohort
Pharmacokinetic Parameters of SCB0020160 for AUCinf
Tidsramme: Up to Day 8 (Part A), Up to Day 21 (Part B), and Up to Day 29 for the Food Effect Cohort
The results of the outcome are collectively measured
Up to Day 8 (Part A), Up to Day 21 (Part B), and Up to Day 29 for the Food Effect Cohort
Pharmacokinetic Parameters of SCB0020160 for t½
Tidsramme: Up to Day 8 (Part A), Up to Day 21 (Part B), and Up to Day 29 for the Food Effect Cohort
The results of the outcome are collectively measured
Up to Day 8 (Part A), Up to Day 21 (Part B), and Up to Day 29 for the Food Effect Cohort
Pharmacokinetic Parameters of SCB0020160 for CL/F
Tidsramme: Up to Day 8 (Part A), Up to Day 21 (Part B), and Up to Day 29 for the Food Effect Cohort
The results of the outcome are collectively measured
Up to Day 8 (Part A), Up to Day 21 (Part B), and Up to Day 29 for the Food Effect Cohort
Pharmacokinetic Parameters of SCB0020160 for Vz/F
Tidsramme: Up to Day 8 (Part A), Up to Day 21 (Part B), and Up to Day 29 for the Food Effect Cohort
The results of the outcome are collectively measured
Up to Day 8 (Part A), Up to Day 21 (Part B), and Up to Day 29 for the Food Effect Cohort
Pharmacokinetic Parameters of SCB0020160 for MRT
Tidsramme: Up to Day 8 (Part A), Up to Day 21 (Part B), and Up to Day 29 for the Food Effect Cohort
The results of the outcome are collectively measured
Up to Day 8 (Part A), Up to Day 21 (Part B), and Up to Day 29 for the Food Effect Cohort

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Comparison of pharmacokinetic parameters for Cmax of SCB0020160 under fasting and fed conditions following a single oral dose.
Tidsramme: Up to Day 29.
The results of the outcome are collectively measured
Up to Day 29.
Comparison of pharmacokinetic parameters for Tmax of SCB0020160 under fasting and fed conditions following a single oral dose.
Tidsramme: Up to Day 29.
The results of the outcome are collectively measured
Up to Day 29.
Comparison of pharmacokinetic parameters for Tlag of SCB0020160 under fasting and fed conditions following a single oral dose.
Tidsramme: Up to Day 29.
The results of the outcome are collectively measured
Up to Day 29.
Comparison of pharmacokinetic parameters for AUClast of SCB0020160 under fasting and fed conditions following a single oral dose.
Tidsramme: Up to Day 29.
The results of the outcome are collectively measured
Up to Day 29.
Comparison of pharmacokinetic parameters for AUCinf of SCB0020160 under fasting and fed conditions following a single oral dose.
Tidsramme: Up to Day 29.
The results of the outcome are collectively measured
Up to Day 29.
Comparison of pharmacokinetic parameters for MRT of SCB0020160 under fasting and fed conditions following a single oral dose.
Tidsramme: Up to Day 29.
The results of the outcome are collectively measured
Up to Day 29.

Samarbeidspartnere og etterforskere

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

Sponsor

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)

29. juni 2026

Primær fullføring (Antatt)

1. juni 2027

Studiet fullført (Antatt)

1. juli 2027

Datoer for studieregistrering

Først innsendt

10. juni 2026

Først innsendt som oppfylte QC-kriteriene

26. juni 2026

Først lagt ut (Faktiske)

2. juli 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

2. juli 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

26. juni 2026

Sist bekreftet

1. juni 2026

Mer informasjon

Begreper knyttet til denne studien

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

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Abonnere