- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07636928
Mass Balance and Absolute Oral Bioavailability of [14C]VH4524184
29 juin 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]VH4524184 in Healthy Participants
The purpose of the study is to assess the bioavailability, mass balance, pharmacokinetics, metabolism and excretion of radiolabeled (14C) VH4524184.
Aperçu de l'étude
Statut
Recrutement
Les conditions
Intervention / Traitement
Type d'étude
Interventionnel
Inscription (Estimé)
9
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
- Nom: US GSK Clinical Trials Call Center
- Numéro de téléphone: 877-379-3718
- E-mail: GSKClinicalSupportHD@gsk.com
Sauvegarde des contacts de l'étude
- Nom: EU GSK Clinical Trials Call Center
- Numéro de téléphone: +44 (0) 20 89904466
- E-mail: GSKClinicalSupportHD@gsk.com
Lieux d'étude
-
-
-
Groningen, Pays-Bas, 9728 NZ
- Recrutement
- GSK Investigational Site
-
Contact:
- US GSK Clinical Trials Call Center
- Numéro de téléphone: 877-379-3718
- E-mail: GSKClinicalSupportHD@gsk.com
-
Contact:
- EU GSK Clinical Trials Call Centre
- Numéro de téléphone: +44 (0) 20 8990 4466
- E-mail: GSKClinicalSupportHD@gsk.com
-
Chercheur principal:
- Renger Tiessen
-
-
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
- Adulte
Accepte les volontaires sains
Oui
La description
Inclusion Criteria:
- Willing and able to sign the Informed Consent Form (ICF).
- Sex at birth: male or female; female participants must be of non-childbearing potential, or postmenopausal.
- Age: 18 to 55 years, inclusive, at screening.
- BMI: 18.0 to 32.0 kg/m^2, inclusive, at screening.
- Female participants of non-childbearing potential must have unequivocal documentation that they are not of childbearing potential 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 and who have a female partner of childbearing potential, must agree to use a condom during any sexual intercourse until the completion of the follow-up visit.
- Male participants must agree not to donate sperm from admission on Day -1 until the completion of the follow-up visit.
- All prescribed medication must have been stopped at least 30 days and >5 half-lives prior to admission to the clinical site on Day -1.
- 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 on Day -1. An exception is made for paracetamol that is allowed up to admission to the clinical site on Day -1.
- Ability and willingness to abstain from alcohol from 48 hours prior to screening and admission to the clinical site on Day -1 until the last PK sample.
- Ability and willingness to abstain from methylxanthine-containing beverages or food (coffee, black tea, green tea, white tea, cola, chocolate, energy drinks), and grapefruit (juice) from 48 hours prior to admission to the clinical site.
- Good physical and mental health based on medical history, physical examination, clinical laboratory, electrocardiogram (ECG), and vital signs, as judged by the Investigator.
Exclusion Criteria:
- Employee of ICON, the Sponsor, GSK or associated vendors.
- 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 study drug.
- Using tobacco/nicotine products within 60 days prior to the first study drug administration.
- History of alcohol abuse or drug addiction within 5 years prior to screening.
- Positive drug and/or alcohol screen at screening or admission to the clinical site.
- Average intake of more than 24 units of alcohol per week.
- Positive screen for hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibodies, or human immunodeficiency virus (HIV) 1 and 2 antibodies at screening.
- Participation in a drug study with a small molecule drug within 30 days or 5 half-lives if known (whichever is longer) prior to the first study drug administration in the current study. Participation in a clinical study with a biological within 90 days or 5 half-lives if known (whichever is longer) prior to the first study drug administration in the current study. Participation in 4 or more other drug studies in the 12 months prior to the first study drug administration in the current study.
- Donation or loss of more than 450 mL of blood within 60 days prior to the first study drug administration. Donation or loss of more than 1.5 L of blood (for male participants)/more than 1.0 L of blood (for female participants) in the 10 months prior to the first study drug administration in the current study.
- Significant and/or acute illness within 14 days prior to the first study drug administration that may impact safety assessments, in the opinion of the Investigator.
- Any significant current/ongoing known or suspected pre-existing psychiatric condition, including depression, anxiety, and/or insomnia/sleep disturbances and/or suicidal ideation, in the opinion of the Investigator.
- Unsuitable veins for infusion or blood sampling.
- Participation in a study with a 14C dose of ≥0.1 megabecquerel (MBq) in the period of 1 year prior to screening.
- Irregular defecation pattern.
- Pre-existing clinically relevant, in the opinion of the Investigator in discussion with the Sponsor medical monitor, gastro-intestinal pathology or diagnosis, eg, irritable bowel syndrome, inflammatory bowel disease, and/or significant baseline signs and symptoms.
- History or presence of clinical condition or disorder that could be capable of significantly altering the absorption, metabolism, or elimination of drugs; constituting a risk when taking the study drugs, interfering with the interpretation of data or would make the participant unsuitable for the study; unable to comply with dosing requirements; or unable to comply with study visits, in the opinion of the Investigator. The Investigator may contact the Sponsor medical monitor to discuss the inclusion of participants who have a history of specific conditions that are not expected to interfere with their participation in the study.
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: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: VH4524184 Group
Participants will receive a dose of VH4524184 under fasting conditions, followed by a microdose of radiolabelled [14C]VH4524184 administered 2.5 hours after first dose administration at time zero on Day 1 (Period1).
After a 14 days wash-out period participants will receive a radiolabelled dose of [14C]VH4524184 on Day 15 under fasting conditions.
|
One dose of VH4524184 is administered to participants at time zero on Day 1 (Period 1).
A radiolabelled microdose of [14C]VH4524184 is administered 2.5 hours after VH4524184 dose administration on Day 1 (Period1).
One dose of radiolabelled [14C]VH4524184 is administered to participants at Day 15 (Period 2).
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Absolute bioavailability (F oral) of VH4524184 (Period 1)
Délai: Day 1 up to Day 14
|
Day 1 up to Day 14
|
|
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Amount of total radioactivity (TRA) excreted in urine (Ae urine) (Period 1)
Délai: Day 1 up to Day 14
|
Urine is collected until amount of radioactivity recovered in excreta (urine and feces) is at least 90% of administered radioactivity and <1% has been recovered from excreta from 2 consecutive days (ie, the total for urine and feces is <1% on 2 consecutive days).
|
Day 1 up to Day 14
|
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Amount of TRA excreted in urine (Ae urine) (Period 2)
Délai: Day 15 up to Day 43
|
Urine is collected until amount of radioactivity recovered in excreta (urine and feces) is at least 90% of administered radioactivity and <1% has been recovered from excreta from 2 consecutive days (ie, the total for urine and feces is <1% on 2 consecutive days).
|
Day 15 up to Day 43
|
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Amount of TRA excreted in feces (Ae feces) (Period 1)
Délai: Day 1 up to Day 14
|
Feces are collected until amount of radioactivity recovered in excreta (urine and feces) is at least 90% of administered radioactivity and <1% has been recovered from excreta from 2 consecutive days (ie, the total for urine and feces is <1% on 2 consecutive days).
|
Day 1 up to Day 14
|
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Amount of TRA excreted in feces (Ae feces) (Period 2)
Délai: Day 15 up to Day 43
|
Feces are collected until amount of radioactivity recovered in excreta (urine and feces) is at least 90% of administered radioactivity and <1% has been recovered from excreta from 2 consecutive days (ie, the total for urine and feces is <1% on 2 consecutive days).
|
Day 15 up to Day 43
|
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Amount of TRA excreted in vomitus (Ae vomit) (Period 1)
Délai: At Day 1
|
At Day 1
|
|
|
Amount of TRA excreted in vomitus (Ae vomit) (Period 2)
Délai: At Day 15
|
At Day 15
|
|
|
Total amount of TRA excreted (Ae total) (Period 1)
Délai: From Day 1 up to Day 14
|
The Ae of TRA measured in urine, feces and vomitus (if applicable on Day 1 only).
Urine and feces are collected until amount of radioactivity recovered in excreta (urine and feces) is at least 90% of administered radioactivity and <1% has been recovered from excreta from 2 consecutive days (ie, the total for urine and feces is <1% on 2 consecutive days).
|
From Day 1 up to Day 14
|
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Total amount of TRA excreted (Ae total) (Period 2)
Délai: Day 15 up to Day 43
|
The Ae of TRA measured in urine, feces and vomitus (if applicable on Day 15 only).
Urine and feces are collected until amount of radioactivity recovered in excreta (urine and feces) is at least 90% of administered radioactivity and <1% has been recovered from excreta from 2 consecutive days (ie, the total for urine and feces is <1% on 2 consecutive days).
|
Day 15 up to Day 43
|
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Fraction of TRA excreted in urine (fe urine) (Period 1)
Délai: Day 1 up to Day 14
|
Urine is collected until the amount of radioactivity recovered in excreta (urine and feces) is at least 90% of administered radioactivity and <1% has been recovered from excreta from 2 consecutive days (ie, the total for urine and feces is <1% on 2 consecutive days).
|
Day 1 up to Day 14
|
|
Fraction of TRA excreted in urine (fe urine) (Period 2)
Délai: Day 15 up to Day 43
|
Urine is collected until amount of radioactivity recovered in excreta (urine and feces) is at least 90% of administered radioactivity and <1% has been recovered from excreta from 2 consecutive days (ie, the total for urine and feces is <1% on 2 consecutive days).
|
Day 15 up to Day 43
|
|
Fraction of TRA excreted in feces (fe feces) (Period 1)
Délai: Day 1 up to Day 14
|
Feces is collected until amount of radioactivity recovered in excreta (urine and feces) is at least 90% of administered radioactivity and <1% has been recovered from excreta from 2 consecutive days (ie, the total for urine and feces is <1% on 2 consecutive days).
|
Day 1 up to Day 14
|
|
Fraction of TRA excreted in feces (fe feces) (Period 2)
Délai: Day 15 up to Day 43
|
Feces is collected until amount of radioactivity recovered in excreta (urine and feces) is at least 90% of administered radioactivity and <1% has been recovered from excreta from 2 consecutive days (ie, the total for urine and feces is <1% on 2 consecutive days).
|
Day 15 up to Day 43
|
|
Fraction of TRA excreted in vomitus (fe vomit) (Period 1)
Délai: At Day 1
|
At Day 1
|
|
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Fraction of TRA excreted in vomitus (fe vomit) (Period 2)
Délai: At Day 15
|
At Day 15
|
|
|
Total fraction of TRA excreted (fe total) (Period 1)
Délai: Day 1 up to Day 14
|
The fe of TRA measured in urine, feces and vomitus (if applicable on Day 1 only).
Urine and feces are collected until amount of radioactivity recovered in excreta (urine and feces) is at least 90% of administered radioactivity and <1% has been recovered from excreta from 2 consecutive days (ie, the total for urine and feces is <1% on 2 consecutive days).
|
Day 1 up to Day 14
|
|
Total fraction of TRA excreted (fe total) (Period 2)
Délai: Day 15 up to Day 43
|
The fe of TRA measured in urine, feces and vomitus (if applicable on Day 15 only).
Urine and feces are collected until amount of radioactivity recovered in excreta (urine and feces) is at least 90% of administered radioactivity and <1% has been recovered from excreta from 2 consecutive days (ie, the total for urine and feces is <1% on 2 consecutive days).
|
Day 15 up to Day 43
|
|
Maximum concentration (Cmax) of VH4524184 in plasma (Period 1)
Délai: Day 1 to Day 14
|
Day 1 to Day 14
|
|
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Maximum concentration (Cmax) of VH4524184 in plasma (Period 2)
Délai: Day 15 to Day 43
|
Day 15 to Day 43
|
|
|
Maximum concentration (Cmax) of [14C]VH4524184 in plasma (Period 1)
Délai: Day 1 to Day 14
|
Day 1 to Day 14
|
|
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Maximum concentration (Cmax) of TRA in plasma (Period 1)
Délai: Day 1 to Day 14
|
Day 1 to Day 14
|
|
|
Maximum concentration (Cmax) of TRA in plasma (Period 2)
Délai: Day 15 to Day 43
|
Day 15 to Day 43
|
|
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Cmax of TRA in whole blood (Period 1)
Délai: Day 1 to Day 14
|
Day 1 to Day 14
|
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Cmax of TRA in whole blood (Period 2)
Délai: Day 15 to Day 43
|
Day 15 to Day 43
|
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Time to maximum concentration (tmax) of VH4524184 in plasma (Period 1)
Délai: Day 1 to Day 14
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Day 1 to Day 14
|
|
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Time to maximum concentration (tmax) of VH4524184 in plasma (Period 2)
Délai: Day 15 to Day 43
|
Day 15 to Day 43
|
|
|
Time to maximum concentration (tmax) of [14C]VH4524184 in plasma (Period 1)
Délai: Day 1 to Day 14
|
Day 1 to Day 14
|
|
|
Time to maximum concentration (tmax) of TRA in plasma (Period 1)
Délai: Day 1 to Day 14
|
Day 1 to Day 14
|
|
|
Time to maximum concentration (tmax) of TRA in plasma (Period 2)
Délai: Day 15 to Day 43
|
Day 15 to Day 43
|
|
|
Time to maximum concentration (tmax) of TRA in whole blood (Period 1)
Délai: Day 1 to Day 14
|
Day 1 to Day 14
|
|
|
Time to maximum concentration (tmax) of TRA in whole blood (Period 2)
Délai: Day 15 to Day 43
|
Day 15 to Day 43
|
|
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Area under the concentration-time curve from time zero to the last measured timepoint (AUC 0-t) of VH4524184 in plasma (Period 1)
Délai: Day 1 to Day 14
|
Day 1 to Day 14
|
|
|
Area under the concentration-time curve from time zero to the last measured timepoint (AUC 0-t) of VH4524184 in plasma (Period 2)
Délai: Day 15 to Day 43
|
Day 15 to Day 43
|
|
|
Area under the concentration-time curve from time zero to the last measured timepoint (AUC 0-t) of [14C]VH4524184 in plasma (Period 1)
Délai: Day 1 to Day 14
|
Day 1 to Day 14
|
|
|
Area under the concentration-time curve from time zero to the last measured timepoint (AUC 0-t) of TRA in plasma (Period 1)
Délai: Day 1 to Day 14
|
Day 1 to Day 14
|
|
|
Area under the concentration-time curve from time zero to the last measured timepoint (AUC 0-t) of TRA in plasma (Period 2)
Délai: Day 15 to Day 43
|
Day 15 to Day 43
|
|
|
Area under the concentration-time curve from time zero to the last measured timepoint (AUC 0-t) of TRA in whole blood (Period 1)
Délai: Day 1 to Day 14
|
Day 1 to Day 14
|
|
|
Area under the concentration-time curve from time zero to the last measured timepoint (AUC 0-t) of TRA in whole blood (Period 2)
Délai: Day 15 to Day 43
|
Day 15 to Day 43
|
|
|
Area under the concentration-time curve from time zero to infinity (AUC 0-inf) of VH4524184 in plasma (Period 1)
Délai: Day 1 to Day 14
|
Day 1 to Day 14
|
|
|
Area under the concentration-time curve from time zero to infinity (AUC 0-inf) of VH4524184 in plasma (Period 2)
Délai: Day 15 up to Day 43
|
Day 15 up to Day 43
|
|
|
Area under the concentration-time curve from time zero to infinity (AUC 0-inf) of [14C]VH4524184 in plasma (Period 1)
Délai: Day 1 to Day 14
|
Day 1 to Day 14
|
|
|
Area under the concentration-time curve from time zero to infinity (AUC 0-inf) of TRA in plasma (Period 1)
Délai: Day 1 to Day 14
|
Day 1 to Day 14
|
|
|
Area under the concentration-time curve from time zero to infinity (AUC 0-inf) of TRA in plasma (Period 2)
Délai: Day 15 to 43
|
Day 15 to 43
|
|
|
Area under the concentration-time curve from time zero to infinity (AUC 0-inf) of TRA in whole blood (Period 1)
Délai: Day 1 to Day 14
|
Day 1 to Day 14
|
|
|
Area under the concentration-time curve from time zero to infinity (AUC 0-inf) of TRA in whole blood (Period 2)
Délai: Day 15 to Day 43
|
Day 15 to Day 43
|
|
|
Amount of VH4524184 excreted in urine (Ae urine) (Period 2)
Délai: Day 15 to Day 43
|
Day 15 to Day 43
|
|
|
Fraction of VH4524184 excreted in urine (fe urine) (Period 2)
Délai: Day 15 to Day 43
|
Day 15 to Day 43
|
|
|
Renal clearance of VH4524184 (CL R) (Period 2)
Délai: Day 15 to Day 43
|
Day 15 to Day 43
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Number of participants with adverse events (AE), overall and by severity (Periods 1 and 2)
Délai: Day 1 to Day 50
|
Day 1 to Day 50
|
|
|
Number of participants who discontinue treatment due to AEs (Periods 1 and 2)
Délai: Day 1 to Day 50
|
Day 1 to Day 50
|
|
|
Change from baseline for aspartate aminotransferase (AST), alanine aminotransferase (ALT), total bilirubin, and alkaline phosphatase (Periods 1 and 2)
Délai: On Days 2, 14, 16, 28 and 42
|
On Days 2, 14, 16, 28 and 42
|
|
|
Maximum toxicity grade increase from baseline for AST, ALT, total bilirubin, and alkaline phosphatase (Periods 1 and 2)
Délai: On Days 2, 14, 16, 28 and 42
|
On Days 2, 14, 16, 28 and 42
|
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|
Blood to plasma ratio of TRA (Periods 1 and 2)
Délai: Day 1 to Day 14 (Period 1) and Day 15 to Day 28 (Period 2)
|
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 in Period 1 and Period 2.
|
Day 1 to Day 14 (Period 1) and Day 15 to Day 28 (Period 2)
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Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
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 (Réel)
4 juin 2026
Achèvement primaire (Estimé)
20 août 2026
Achèvement de l'étude (Estimé)
20 août 2026
Dates d'inscription aux études
Première soumission
29 mai 2026
Première soumission répondant aux critères de contrôle qualité
3 juin 2026
Première publication (Réel)
9 juin 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
2 juillet 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
29 juin 2026
Dernière vérification
1 juin 2026
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Infections transmissibles par le sang
- Maladies urogénitales
- Maladies génitales
- Maladies du système immunitaire
- Infections
- Infections par virus à ARN
- Maladies virales
- Maladies transmissibles
- Maladies sexuellement transmissibles, virales
- Maladies sexuellement transmissibles
- Infections à lentivirus
- Infections à rétroviridae
- Syndromes d'immunodéficience
- Maladies à virus lents
- Infections à VIH
- Syndrome immunodéficitaire acquis
Autres numéros d'identification d'étude
- 223803
- 2026-525590-40 (Autre identifiant: EU CT Number)
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_25Sep2023.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 .