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Mass Balance and Absolute Bioavailability of [14C]-VH4011499

6 novembre 2026 mis à jour par: ViiV Healthcare

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.

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Estimé)

18

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Sauvegarde des contacts de l'étude

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 55 ans (Adulte)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

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.

  • Age: 18 to 55 years, inclusive, at screening.

  • 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.
  • 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.

  • 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.

  • 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.

  • 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.

  • 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).

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Science basique
  • Répartition: Non randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 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.

Expérimental: VH4011499 Cohort 2

Participants will receive a single oral dose of [14C]-VH4011499.

[14C]-VH4011499 will be administered orally.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Total Radioactivity (TRA) of the Cumulative Amount of Drug Excreted in Urine (Ae urine)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: Up to 70 days
Up to 70 days
Time to Attain Cmax (tmax) of VH4011499
Délai: 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
Délai: Up to 70 days
Up to 70 days
Area Under the Plasma Concentration-time Curve From Time 0 to Infinity (AUC0-inf) of VH4011499
Délai: Up to 70 days
Up to 70 days
Cohort 1 Only: Cmax of [14C]-VH4011499
Délai: Up to 70 days
Up to 70 days
Cohort 1 Only: Tmax of [14C]-VH4011499
Délai: Up to 70 days
Up to 70 days
Cohort 1 Only: AUC0-t of [14C]-VH4011499
Délai: Up to 70 days
Up to 70 days
Cohort 1 Only: AUC0-inf of [14C]-VH4011499
Délai: Up to 70 days
Up to 70 days
Cmax of TRA in Plasma
Délai: Up to 70 days
Up to 70 days
Tmax of TRA in Plasma
Délai: Up to 70 days
Up to 70 days
AUC0-t of TRA in Plasma
Délai: Up to 70 days
Up to 70 days
AUC0-inf of TRA in Plasma
Délai: Up to 70 days
Up to 70 days
Cmax of TRA in Whole Blood
Délai: Up to 70 days
Up to 70 days
Tmax of TRA in Whole Blood
Délai: Up to 70 days
Up to 70 days
AUC0-t of TRA in Whole Blood
Délai: Up to 70 days
Up to 70 days
AUC0-inf of TRA in Whole Blood
Délai: Up to 70 days
Up to 70 days
Whole Blood-to-plasma Ratio of TRA
Délai: 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
Délai: Up to 70 days
Up to 70 days
Cohort 2 Only: fe urine of VH4011499
Délai: 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
Délai: Up to 70 days
Up to 70 days

Mesures de résultats secondaires

Mesure des résultats
Délai
Number of Participants with Adverse Events (AEs) by Severity
Délai: 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)
Délai: Up to 77 days
Up to 77 days
Change From Baseline in Total Bilirubin, Direct Bilirubin, ALP, AST, and ALT
Délai: Up to 77 days
Up to 77 days
Maximum Toxicity Grade Change From Baseline in Total Bilirubin, Direct Bilirubin, ALP, AST, and ALT
Délai: Up to 77 days
Up to 77 days
Cohort 1 Only: Absolute Oral Bioavailability (F oral) of VH4011499
Délai: Up to 70 days
Up to 70 days

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Les enquêteurs

  • Directeur d'études: GSK Clinical Trials, GlaxoSmithKline

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

9 novembre 2026

Achèvement primaire (Estimé)

18 février 2027

Achèvement de l'étude (Estimé)

18 février 2027

Dates d'inscription aux études

Première soumission

6 novembre 2026

Première soumission répondant aux critères de contrôle qualité

6 novembre 2026

Première publication (Réel)

13 novembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

13 novembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

6 novembre 2026

Dernière vérification

1 novembre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

OUI

Description du régime 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

Délai de partage 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.

Critères d'accès au partage 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.

Type d'informations de prise en charge du partage d'IPD

  • PROTOCOLE D'ÉTUDE
  • SÈVE
  • CIF
  • RSE

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Oui

Étudie un produit d'appareil réglementé par la FDA américaine

Non

produit fabriqué et exporté des États-Unis.

Oui

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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