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.
Visão geral do estudo
Status
Status
Condições
Condições
Intervenção / Tratamento
Intervenção / Tratamento
Tipo de estudo
Tipo de estudo
Inscrição (Estimado)
Inscrição
Estágio
Estágio
- Fase 1
Contactos e Locais
Contato de estudo
Contato de estudo
- Nome: US GSK Clinical Trials Call Center
- Número de telefone: 877-379-3718
- E-mail: GSKClinicalSupportHD@gsk.com
Estude backup de contato
- Nome: EU GSK Clinical Trials Call Center
- Número de telefone: +44 (0) 20 89904466
- E-mail: GSKClinicalSupportHD@gsk.com
Critérios de participação
Critérios de elegibilidade
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
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).
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Ciência básica
- Alocação: Não randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Nenhum (rótulo aberto)
Número de braços
Armas e Intervenções
Grupo de Participantes / BraçoGrupo de Participantes / Braço |
Intervenção / TratamentoIntervenção / Tratamento |
|---|---|
|
Experimental: 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. |
|
Experimental: VH4011499 Cohort 2
Participants will receive a single oral dose of [14C]-VH4011499. |
[14C]-VH4011499 will be administered orally. |
O que o estudo está medindo?
Medidas de resultados primários
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Total Radioactivity (TRA) of the Cumulative Amount of Drug Excreted in Urine (Ae urine)
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: Up to 70 days
|
Up to 70 days
|
|
|
Time to Attain Cmax (tmax) of VH4011499
Prazo: 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
Prazo: Up to 70 days
|
Up to 70 days
|
|
|
Area Under the Plasma Concentration-time Curve From Time 0 to Infinity (AUC0-inf) of VH4011499
Prazo: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 1 Only: Cmax of [14C]-VH4011499
Prazo: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 1 Only: Tmax of [14C]-VH4011499
Prazo: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 1 Only: AUC0-t of [14C]-VH4011499
Prazo: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 1 Only: AUC0-inf of [14C]-VH4011499
Prazo: Up to 70 days
|
Up to 70 days
|
|
|
Cmax of TRA in Plasma
Prazo: Up to 70 days
|
Up to 70 days
|
|
|
Tmax of TRA in Plasma
Prazo: Up to 70 days
|
Up to 70 days
|
|
|
AUC0-t of TRA in Plasma
Prazo: Up to 70 days
|
Up to 70 days
|
|
|
AUC0-inf of TRA in Plasma
Prazo: Up to 70 days
|
Up to 70 days
|
|
|
Cmax of TRA in Whole Blood
Prazo: Up to 70 days
|
Up to 70 days
|
|
|
Tmax of TRA in Whole Blood
Prazo: Up to 70 days
|
Up to 70 days
|
|
|
AUC0-t of TRA in Whole Blood
Prazo: Up to 70 days
|
Up to 70 days
|
|
|
AUC0-inf of TRA in Whole Blood
Prazo: Up to 70 days
|
Up to 70 days
|
|
|
Whole Blood-to-plasma Ratio of TRA
Prazo: 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
Prazo: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 2 Only: fe urine of VH4011499
Prazo: 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
Prazo: Up to 70 days
|
Up to 70 days
|
Medidas de resultados secundários
Medidas de resultados secundários
Medida de resultado |
Prazo |
|---|---|
|
Number of Participants with Adverse Events (AEs) by Severity
Prazo: 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)
Prazo: Up to 77 days
|
Up to 77 days
|
|
Change From Baseline in Total Bilirubin, Direct Bilirubin, ALP, AST, and ALT
Prazo: Up to 77 days
|
Up to 77 days
|
|
Maximum Toxicity Grade Change From Baseline in Total Bilirubin, Direct Bilirubin, ALP, AST, and ALT
Prazo: Up to 77 days
|
Up to 77 days
|
|
Cohort 1 Only: Absolute Oral Bioavailability (F oral) of VH4011499
Prazo: Up to 70 days
|
Up to 70 days
|
Colaboradores e Investigadores
Patrocinador
Patrocinador
Investigadores
Investigadores
- Diretor de estudo: GSK Clinical Trials, GlaxoSmithKline
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Início do estudo
Conclusão Primária (Estimado)
Conclusão Primária
Conclusão do estudo (Estimado)
Conclusão do estudo
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Primeira postagem
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última Atualização Postada
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
- Infecções transmitidas pelo sangue
- Doenças urogenitais
- Doenças Genitais
- Doenças do sistema imunológico
- Infecções
- Infecções por vírus de RNA
- Doenças Virais
- Doenças Transmissíveis
- Doenças Sexualmente Transmissíveis, Virais
- Doenças Sexualmente Transmissíveis
- Infecções por Lentivírus
- Infecções por Retroviridae
- Síndromes de Deficiência Imunológica
- Doenças de Vírus Lento
- Infecções por HIV
- Síndrome da Imunodeficiência Adquirida
Outros números de identificação do estudo
Outros números de identificação do estudo
- 223808
- 2026-527050-40 (Outro identificador: EU CT number)
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Descrição do plano 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
Prazo de Compartilhamento de 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.
Critérios de acesso de compartilhamento 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.
Tipo de informação de suporte de compartilhamento de IPD
- PROTOCOLO DE ESTUDO
- SEIVA
- CIF
- CSR
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
produto fabricado e exportado dos EUA
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .