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.
Przegląd badań
Status
Status
Warunki
Warunki
Interwencja / Leczenie
Interwencja / Leczenie
Typ studiów
Typ studiów
Zapisy (Szacowany)
Zapisy
Faza
Faza
- Faza 1
Kontakty i lokalizacje
Kontakt w sprawie studiów
Kontakt w sprawie studiów
- Nazwa: US GSK Clinical Trials Call Center
- Numer telefonu: 877-379-3718
- E-mail: GSKClinicalSupportHD@gsk.com
Kopia zapasowa kontaktu do badania
- Nazwa: EU GSK Clinical Trials Call Center
- Numer telefonu: +44 (0) 20 89904466
- E-mail: GSKClinicalSupportHD@gsk.com
Kryteria uczestnictwa
Kryteria kwalifikacji
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
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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.
-
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).
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Podstawowa nauka
- Przydział: Nielosowe
- Model interwencyjny: Przydział równoległy
- Maskowanie: Brak (otwarta etykieta)
Liczba ramion
Broń i interwencje
Grupa uczestników / ArmGrupa uczestników / Arm |
Interwencja / LeczenieInterwencja / Leczenie |
|---|---|
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Eksperymentalny: 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. |
|
Eksperymentalny: VH4011499 Cohort 2
Participants will receive a single oral dose of [14C]-VH4011499. |
[14C]-VH4011499 will be administered orally. |
Co mierzy badanie?
Podstawowe miary wyniku
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Total Radioactivity (TRA) of the Cumulative Amount of Drug Excreted in Urine (Ae urine)
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
|
|
Time to Attain Cmax (tmax) of VH4011499
Ramy czasowe: 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
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
|
|
Area Under the Plasma Concentration-time Curve From Time 0 to Infinity (AUC0-inf) of VH4011499
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 1 Only: Cmax of [14C]-VH4011499
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 1 Only: Tmax of [14C]-VH4011499
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 1 Only: AUC0-t of [14C]-VH4011499
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 1 Only: AUC0-inf of [14C]-VH4011499
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
|
|
Cmax of TRA in Plasma
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
|
|
Tmax of TRA in Plasma
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
|
|
AUC0-t of TRA in Plasma
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
|
|
AUC0-inf of TRA in Plasma
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
|
|
Cmax of TRA in Whole Blood
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
|
|
Tmax of TRA in Whole Blood
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
|
|
AUC0-t of TRA in Whole Blood
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
|
|
AUC0-inf of TRA in Whole Blood
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
|
|
Whole Blood-to-plasma Ratio of TRA
Ramy czasowe: 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
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 2 Only: fe urine of VH4011499
Ramy czasowe: 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
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
Miary wyników drugorzędnych
Miary wyników drugorzędnych
Miara wyniku |
Ramy czasowe |
|---|---|
|
Number of Participants with Adverse Events (AEs) by Severity
Ramy czasowe: 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)
Ramy czasowe: Up to 77 days
|
Up to 77 days
|
|
Change From Baseline in Total Bilirubin, Direct Bilirubin, ALP, AST, and ALT
Ramy czasowe: Up to 77 days
|
Up to 77 days
|
|
Maximum Toxicity Grade Change From Baseline in Total Bilirubin, Direct Bilirubin, ALP, AST, and ALT
Ramy czasowe: Up to 77 days
|
Up to 77 days
|
|
Cohort 1 Only: Absolute Oral Bioavailability (F oral) of VH4011499
Ramy czasowe: Up to 70 days
|
Up to 70 days
|
Współpracownicy i badacze
Sponsor
Sponsor
Śledczy
Śledczy
- Dyrektor Studium: GSK Clinical Trials, GlaxoSmithKline
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Szacowany)
Rozpoczęcie studiów
Zakończenie podstawowe (Szacowany)
Zakończenie podstawowe
Ukończenie studiów (Szacowany)
Ukończenie studiów
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Pierwszy wysłany
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia wysłana aktualizacja
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
- Infekcje przenoszone przez krew
- Choroby układu moczowo-płciowego
- Choroby narządów płciowych
- Choroby układu odpornościowego
- Infekcje
- Zakażenia wirusem RNA
- Choroby wirusowe
- Choroby zakaźne
- Choroby przenoszone drogą płciową, wirusowe
- Choroby przenoszone drogą płciową
- Infekcje lentiwirusowe
- Zakażenia Retroviridae
- Zespoły niedoboru odporności
- Powolne choroby wirusowe
- Zakażenia wirusem HIV
- Zespół nabytego niedoboru odporności
Inne numery identyfikacyjne badania
Inne numery identyfikacyjne badania
- 223808
- 2026-527050-40 (Inny identyfikator: EU CT number)
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Opis planu 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
Ramy czasowe udostępniania 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.
Kryteria dostępu do udostępniania 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 informacji pomocniczych dotyczących udostępniania IPD
- PROTOKÓŁ BADANIA
- SOK ROŚLINNY
- ICF
- CSR
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
produkt wyprodukowany i wyeksportowany z USA
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