- ICH GCP
- USA klinikai vizsgálatok nyilvántartása
- Klinikai vizsgálat 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.
A tanulmány áttekintése
Állapot
Körülmények
Beavatkozás / kezelés
Tanulmány típusa
Beiratkozás (Becsült)
Fázis
- 1. fázis
Kapcsolatok és helyek
Tanulmányi kapcsolat
- Név: US GSK Clinical Trials Call Center
- Telefonszám: 877-379-3718
- E-mail: GSKClinicalSupportHD@gsk.com
Tanulmányozza a kapcsolattartók biztonsági mentését
- Név: EU GSK Clinical Trials Call Center
- Telefonszám: +44 (0) 20 89904466
- E-mail: GSKClinicalSupportHD@gsk.com
Részvételi kritériumok
Jogosultsági kritériumok
Tanulmányozható életkorok
Egészséges önkénteseket fogad
Tanulmányozható nemek
Leírás
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.
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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).
Tanulási terv
Hogyan készül a tanulmány?
Tervezési részletek
- Elsődleges cél: Alapvető tudomány
- Kiosztás: Nem véletlenszerű
- Beavatkozó modell: Párhuzamos hozzárendelés
- Maszkolás: Nincs (Open Label)
Fegyverek és beavatkozások
Résztvevő csoport / kar |
Beavatkozás / kezelés |
|---|---|
|
Kísérleti: 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. |
|
Kísérleti: VH4011499 Cohort 2
Participants will receive a single oral dose of [14C]-VH4011499. |
[14C]-VH4011499 will be administered orally. |
Mit mér a tanulmány?
Elsődleges eredményintézkedések
Eredménymérő |
Intézkedés leírása |
Időkeret |
|---|---|---|
|
Total Radioactivity (TRA) of the Cumulative Amount of Drug Excreted in Urine (Ae urine)
Időkeret: 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)
Időkeret: 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)
Időkeret: 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)
Időkeret: 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
Időkeret: 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
Időkeret: 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
Időkeret: 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
Időkeret: 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
Időkeret: Up to 70 days
|
Up to 70 days
|
|
|
Time to Attain Cmax (tmax) of VH4011499
Időkeret: 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
Időkeret: Up to 70 days
|
Up to 70 days
|
|
|
Area Under the Plasma Concentration-time Curve From Time 0 to Infinity (AUC0-inf) of VH4011499
Időkeret: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 1 Only: Cmax of [14C]-VH4011499
Időkeret: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 1 Only: Tmax of [14C]-VH4011499
Időkeret: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 1 Only: AUC0-t of [14C]-VH4011499
Időkeret: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 1 Only: AUC0-inf of [14C]-VH4011499
Időkeret: Up to 70 days
|
Up to 70 days
|
|
|
Cmax of TRA in Plasma
Időkeret: Up to 70 days
|
Up to 70 days
|
|
|
Tmax of TRA in Plasma
Időkeret: Up to 70 days
|
Up to 70 days
|
|
|
AUC0-t of TRA in Plasma
Időkeret: Up to 70 days
|
Up to 70 days
|
|
|
AUC0-inf of TRA in Plasma
Időkeret: Up to 70 days
|
Up to 70 days
|
|
|
Cmax of TRA in Whole Blood
Időkeret: Up to 70 days
|
Up to 70 days
|
|
|
Tmax of TRA in Whole Blood
Időkeret: Up to 70 days
|
Up to 70 days
|
|
|
AUC0-t of TRA in Whole Blood
Időkeret: Up to 70 days
|
Up to 70 days
|
|
|
AUC0-inf of TRA in Whole Blood
Időkeret: Up to 70 days
|
Up to 70 days
|
|
|
Whole Blood-to-plasma Ratio of TRA
Időkeret: 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
Időkeret: Up to 70 days
|
Up to 70 days
|
|
|
Cohort 2 Only: fe urine of VH4011499
Időkeret: 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
Időkeret: Up to 70 days
|
Up to 70 days
|
Másodlagos eredményintézkedések
Eredménymérő |
Időkeret |
|---|---|
|
Number of Participants with Adverse Events (AEs) by Severity
Időkeret: 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)
Időkeret: Up to 77 days
|
Up to 77 days
|
|
Change From Baseline in Total Bilirubin, Direct Bilirubin, ALP, AST, and ALT
Időkeret: Up to 77 days
|
Up to 77 days
|
|
Maximum Toxicity Grade Change From Baseline in Total Bilirubin, Direct Bilirubin, ALP, AST, and ALT
Időkeret: Up to 77 days
|
Up to 77 days
|
|
Cohort 1 Only: Absolute Oral Bioavailability (F oral) of VH4011499
Időkeret: Up to 70 days
|
Up to 70 days
|
Együttműködők és nyomozók
Szponzor
Nyomozók
- Tanulmányi igazgató: GSK Clinical Trials, GlaxoSmithKline
Tanulmányi rekorddátumok
Tanulmány főbb dátumok
Tanulmány kezdete (Becsült)
Elsődleges befejezés (Becsült)
A tanulmány befejezése (Becsült)
Tanulmányi regisztráció dátumai
Először benyújtva
Először nyújtották be, amely megfelel a minőségbiztosítási kritériumoknak
Első közzététel (Tényleges)
Tanulmányi rekordok frissítései
Utolsó frissítés közzétéve (Tényleges)
Az utolsó frissítés elküldve, amely megfelel a minőségbiztosítási kritériumoknak
Utolsó ellenőrzés
Több információ
A tanulmányhoz kapcsolódó kifejezések
Kulcsszavak
További vonatkozó MeSH feltételek
- Vérrel terjedő fertőzések
- Urogenitális betegségek
- Nemi szervek betegségei
- Immunrendszeri betegségek
- Fertőzések
- RNS vírusfertőzések
- Vírusos betegségek
- Fertőző betegségek
- Szexuális úton terjedő betegségek, vírusos
- Szexuális úton terjedő betegségek
- Lentivírus fertőzések
- Retroviridae fertőzések
- Immunhiányos szindrómák
- Lassú vírusos betegségek
- HIV fertőzések
- Szerzett immunhiányos szindróma
Egyéb vizsgálati azonosító számok
- 223808
- 2026-527050-40 (Egyéb azonosító: EU CT number)
Terv az egyéni résztvevői adatokhoz (IPD)
Tervezi megosztani az egyéni résztvevői adatokat (IPD)?
IPD terv leírása
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
IPD megosztási időkeret
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.
IPD-megosztási hozzáférési feltételek
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.
Az IPD megosztását támogató információ típusa
- STUDY_PROTOCOL
- NEDV
- ICF
- CSR
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az Egyesült Államokban gyártott és onnan exportált termék
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