- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT07934719
Mass Balance and Absolute Bioavailability of [14C]-VH4011499
A Phase 1, Open-label, Single-dose Study to Assess the Absolute Bioavailability, Mass Balance, Pharmacokinetics, Metabolism, and Excretion of [14C]-VH4011499 in Healthy Participants
The purpose of the trial is to characterize the absorption, metabolism, and excretion of [14C]-VH4011499, and to evaluate the absolute bioavailability of VH4011499.
Přehled studie
Postavení
Podmínky
Intervence / Léčba
Typ studie
Zápis (Odhadovaný)
Fáze
- Fáze 1
Kontakty a umístění
Studijní kontakt
- Jméno: US GSK Clinical Trials Call Center
- Telefonní číslo: 877-379-3718
- E-mail: GSKClinicalSupportHD@gsk.com
Studijní záloha kontaktů
- Jméno: EU GSK Clinical Trials Call Center
- Telefonní číslo: +44 (0) 20 89904466
- E-mail: GSKClinicalSupportHD@gsk.com
Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
Přijímá zdravé dobrovolníky
Pohlaví způsobilá ke studiu
Popis
Inclusion Criteria:
-
Willing and able to sign the informed consent form.
-
Sex at birth: male or female; female participants must be of non-childbearing potential, or postmenopausal.
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Age: 18 to 55 years, inclusive, at screening.
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Female participants are eligible to participate if they are of non-childbearing potential and are not breastfeeding or planning to breastfeed for at least 12 months following the last dose.
- Female participants of non-childbearing potential must have unequivocal documentation (either by medical records and/or from the clinical interview) that they are not of childbearing potential (postmenopausal, medically sterile, or surgically sterile). Postmenopausal female participants must have a serum follicle-stimulating hormone (FSH) concentration >33.4 milli-international units per milliliter (mIU/mL) at screening to confirm menopause.
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Male participants, if not surgically sterilized, must agree to use a condom when having sexual intercourse with a female partner of childbearing potential from admission to the clinical site on Day -1 until the completion of the follow up visit.
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Male participants must agree not to donate sperm from admission to the clinical site on Day -1 until the completion of the follow-up visit.
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All prescribed medication must have been stopped at least 30 days or >5 half-lives (whichever is longer) prior to admission to the clinical site on Day -1 until completion of the follow-up visit.
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All over-the-counter medication, vitamin preparations and other food supplements, or herbal medications must have been stopped at least 14 days prior to admission to the clinical site until completion of the follow-up visit. An exception is made for paracetamol (≤ 2 g per day), which is allowed up to admission to the clinical site.
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Good physical and mental health based on medical history, physical examination, clinical laboratory test results, electrocardiogram (ECG), and vital signs, as judged by the Investigator.
Exclusion Criteria:
- History of relevant drug and/or food allergies. - History of drug hypersensitivity, delayed-type hypersensitivity, or severe hypersensitivity reactions, as well as history of sensitivity to the trial drug.
- Using tobacco/nicotine products within 30 days prior to the first trial drug administration. - Positive screen for hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibodies, or HIV 1 or 2 antibodies at screening.
- Unstable liver disease (as defined by any of the following: presence of ascites, encephalopathy, coagulopathy, hypoalbuminemia, esophageal or gastric varices, or persistent jaundice or cirrhosis), known biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones or otherwise stable chronic liver disease per investigator assessment).
- Known history of cirrhosis with or without viral hepatitis co-infection.
- History of clinically relevant hepatitis within the last 6 months.
- Any verified Grade 4 laboratory abnormality. - ALT >1.5x (upper limit of normal [ULN]).
- Total bilirubin >1.5x ULN.
- Estimated glomerular filtration rate (GFR) of <60 mL/min/1.73 m^2.
- QT interval corrected for heart rate according to Fridericia's formula (QTcF) >450 msec.
- Clinically significant cardiovascular disease, as defined by history/evidence of congestive heart failure, symptomatic arrhythmia, angina/ischemia, coronary artery bypass grafting surgery or percutaneous transluminal coronary angioplasty or any clinically significant cardiac disease.
- Unsuitable veins for infusion or blood sampling. - Participation in a trial with a [14C] dose of ≥0.1 MBq in the period of 1 year prior to screening.
- TRA in plasma must not exceed a [14C] / [12C] ratio of 1.31x10^-12. - Exposure to significant radiation (e.g., serial x-ray or CT scans, barium meal, etc.) in the 3 years prior to screening.
- Irregular defecation pattern (less than once per 2 days).
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Základní věda
- Přidělení: Nerandomizované
- Intervenční model: Paralelní přiřazení
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
|
Experimentální: VH4011499 Cohort 1
Participants will receive a single oral dose of VH4011499, followed by a single intravenous (iv) microtracer dose of [14C]-VH4011499. |
VH4011499 will be administered orally. [14C]-VH4011499 will be administered as an iv infusion. |
|
Experimentální: VH4011499 Cohort 2
Participants will receive a single oral dose of [14C]-VH4011499. |
[14C]-VH4011499 will be administered orally. |
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Total Radioactivity (TRA) of the Cumulative Amount of Drug Excreted in Urine (Ae urine)
Časové okno: Up to 70 days
|
Urine is collected until the cumulative amount of radioactivity recovered in excreta (urine and feces) is at least 90% of the administered radioactivity and less than 1% of the administered radioactive dose is recovered during a 24-hour collection period on 2 consecutive collection days. |
Up to 70 days
|
|
TRA of the Cumulative Amount of Drug Excreted in Feces (Ae feces)
Časové okno: Up to 70 days
|
Feces are collected until the cumulative amount of radioactivity recovered in excreta (urine and feces) is at least 90% of the administered radioactivity and less than 1% of the administered radioactive dose is recovered during a 24-hour collection period on 2 consecutive collection days. |
Up to 70 days
|
|
Cohort 2 Only: TRA of the Cumulative Amount of Drug Excreted in Vomitus (Ae vomit)
Časové okno: Up to 70 days
|
Vomitus (if applicable) will be collected and included in the assessment until the cumulative amount of radioactivity recovered in excreta is at least 90% of the administered radioactivity and less than 1% of the administered radioactive dose is recovered. |
Up to 70 days
|
|
TRA of the Total Amount of Drug Excreted (Ae total)
Časové okno: Up to 70 days
|
Total amount of TRA excreted in excreta, calculated as the sum of the cumulative amount of radioactivity recovered in urine, feces, and vomit (if collected). Urine, feces, and vomitus (if applicable) will be collected until the cumulative amount of radioactivity recovered in excreta is at least 90% of the administered radioactive dose and less than 1% of the administered radioactive dose is recovered during a 24-hour collection period on 2 consecutive collection days. |
Up to 70 days
|
|
Fraction of the Administered Radiolabeled Dose Excreted in Urine (fe urine) as Total Drug Related Material
Časové okno: Up to 70 days
|
Fraction of the dose administered excreted (unchanged) in urine percentage. Urine is collected until the cumulative amount of radioactivity recovered in excreta (urine and feces) is at least 90% of the administered radioactivity and less than 1% of the administered radioactive dose is recovered during a 24-hour collection period on 2 consecutive collection days. |
Up to 70 days
|
|
Cohort 2 Only: Fraction of the Administered Radiolabeled Dose Excreted in Feces (fe feces) as Total Drug Related Material
Časové okno: Up to 70 days
|
Fraction of the dose administered excreted in feces percentage. Feces are collected until the cumulative amount of radioactivity recovered in excreta (urine and feces) is at least 90% of the administered radioactivity and less than 1% of the administered radioactive dose is recovered during a 24-hour collection period on 2 consecutive collection days. |
Up to 70 days
|
|
Cohort 2 Only: Fraction of the Administered Radiolabeled Dose Excreted in Vomitus (fe vomit) as Total Drug Related Material
Časové okno: Up to 70 days
|
Fraction of the dose administered excreted in vomitus percentage. Vomitus (if applicable) will be collected and included in the assessment until the cumulative amount of radioactivity recovered in excreta is at least 90% of the administered radioactivity and less than 1% of the administered radioactive dose is recovered. |
Up to 70 days
|
|
Fraction of the Administered Radiolabeled Dose Excreted in Urine, Feces, and Vomitus (fe total) as Total Drug Related Material
Časové okno: Up to 70 days
|
Fraction of the dose administered excreted in urine, feces, and vomitus if applicable percentage. Urine, feces, and vomitus (if applicable) will be collected until the cumulative amount of radioactivity recovered in excreta is at least 90% of the administered radioactive dose and less than 1% of the administered radioactive dose is recovered during a 24-hour collection period on 2 consecutive collection days. |
Up to 70 days
|
|
Maximum Observed Plasma Concentration (Cmax) of VH4011499
Časové okno: Up to 70 days
|
Up to 70 days
|
|
|
Time to Attain Cmax (tmax) of VH4011499
Časové okno: Up to 70 days
|
Up to 70 days
|
|
|
Area Under the Plasma Concentration-time Curve From Time Zero to the Last Quantifiable Concentration (AUC0-t) of VH4011499
Časové okno: Up to 70 days
|
Up to 70 days
|
|
|
Area Under the Plasma Concentration-time Curve From Time 0 to Infinity (AUC0-inf) of VH4011499
Časové okno: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 1 Only: Cmax of [14C]-VH4011499
Časové okno: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 1 Only: Tmax of [14C]-VH4011499
Časové okno: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 1 Only: AUC0-t of [14C]-VH4011499
Časové okno: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 1 Only: AUC0-inf of [14C]-VH4011499
Časové okno: Up to 70 days
|
Up to 70 days
|
|
|
Cmax of TRA in Plasma
Časové okno: Up to 70 days
|
Up to 70 days
|
|
|
Tmax of TRA in Plasma
Časové okno: Up to 70 days
|
Up to 70 days
|
|
|
AUC0-t of TRA in Plasma
Časové okno: Up to 70 days
|
Up to 70 days
|
|
|
AUC0-inf of TRA in Plasma
Časové okno: Up to 70 days
|
Up to 70 days
|
|
|
Cmax of TRA in Whole Blood
Časové okno: Up to 70 days
|
Up to 70 days
|
|
|
Tmax of TRA in Whole Blood
Časové okno: Up to 70 days
|
Up to 70 days
|
|
|
AUC0-t of TRA in Whole Blood
Časové okno: Up to 70 days
|
Up to 70 days
|
|
|
AUC0-inf of TRA in Whole Blood
Časové okno: Up to 70 days
|
Up to 70 days
|
|
|
Whole Blood-to-plasma Ratio of TRA
Časové okno: Up to 70 days
|
Cmax, AUC(0-t) and AUC(0-inf) TRA measured in whole blood compared to Cmax, AUC(0-t) and AUC(0-inf) TRA measured in plasma. |
Up to 70 days
|
|
Cohort 2 Only: Ae urine of VH4011499
Časové okno: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 2 Only: fe urine of VH4011499
Časové okno: Up to 70 days
|
Fraction of the dose administered excreted (unchanged) in urine percentage. |
Up to 70 days
|
|
Cohort 2 Only: Renal clearance (CLR) of VH4011499
Časové okno: Up to 70 days
|
Up to 70 days
|
Sekundární výstupní opatření
Měření výsledku |
Časové okno |
|---|---|
|
Number of Participants with Adverse Events (AEs) by Severity
Časové okno: Up to 77 days
|
Up to 77 days
|
|
Absolute Values of Total Bilirubin, Direct bilirubin, Alkaline Phosphatase (ALP), Aspartate Aminotransferase (AST), and Alanine Aminotransferase (ALT)
Časové okno: Up to 77 days
|
Up to 77 days
|
|
Change From Baseline in Total Bilirubin, Direct Bilirubin, ALP, AST, and ALT
Časové okno: Up to 77 days
|
Up to 77 days
|
|
Maximum Toxicity Grade Change From Baseline in Total Bilirubin, Direct Bilirubin, ALP, AST, and ALT
Časové okno: Up to 77 days
|
Up to 77 days
|
|
Cohort 1 Only: Absolute Oral Bioavailability (F oral) of VH4011499
Časové okno: Up to 70 days
|
Up to 70 days
|
Spolupracovníci a vyšetřovatelé
Sponzor
Vyšetřovatelé
- Ředitel studie: GSK Clinical Trials, GlaxoSmithKline
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Odhadovaný)
Primární dokončení (Odhadovaný)
Dokončení studie (Odhadovaný)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
- Infekce přenášené krví
- Urogenitální onemocnění
- Onemocnění genitálií
- Onemocnění imunitního systému
- Infekce
- RNA virové infekce
- Virová onemocnění
- Přenosné nemoci
- Pohlavně přenosné choroby, virové
- Pohlavně přenosné nemoci
- Lentivirové infekce
- Retroviridae infekce
- Syndromy imunologické nedostatečnosti
- Pomalá virová onemocnění
- HIV infekce
- Syndrom získané immunití nedostatečnisti
Další identifikační čísla studie
- 223808
- 2026-527050-40 (Jiný identifikátor: EU CT number)
Plán pro data jednotlivých účastníků (IPD)
Plánujete sdílet data jednotlivých účastníků (IPD)?
Popis plánu IPD
Study Sponsor will assess requests from qualified researchers for anonymized individual patient-level data and related study documents. Data sharing is subject to certain criteria, conditions, and exceptions. For further information, refer to https://www.viiv-studyregister.com/documents/About_ViiV_Patient_Level_Data_Sharing_Final_28May2026.pdf
Časový rámec sdílení IPD
Anonymized IPD will be made available within 6 months of publication of primary, key secondary and safety results for studies in product with approved indication(s) or asset(s) with development terminated across all indications.
Kritéria přístupu pro sdílení IPD
Anonymized IPD is shared with researchers whose proposals are approved by an Independent Review Panel and after a Data Sharing Agreement is in place. Access is provided for an initial period of 12 months, but an extension may be granted, when justified, for up to 6 months.
Typ podpůrných informací pro sdílení IPD
- PROTOKOL STUDY
- MÍZA
- ICF
- CSR
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
produkt vyrobený a vyvážený z USA
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