Status:
COMPLETED
A Study to Investigate the Relative Bioavailability and Food Effect of an Oral Capsid Inhibitor Tablet Formulation Compared With Other Oral Tablet Formulations in Male and Female Healthy Participants
Lead Sponsor:
ViiV Healthcare
Conditions:
HIV Infections
Eligibility:
All Genders
18-55 years
Phase:
PHASE1
Brief Summary
This is a 3 part study of an investigational capsid inhibitor, VH4004280, in healthy adult participants. The purpose is to evaluate the effect of tablet formulation as well as food on bioavailability....
Eligibility Criteria
Inclusion
- Participants must be 18 to 55years of age.
- Participants who are overtly healthy.
- Negative (Severe Acute Respiratory Syndrome Coronavirus 2) SARs-CoV-2 test prior to dosing.
- Has body mass index (BMI) within the range 19-32 (kg/m2).
- Participants male at birth must use male condoms, and participants female at birth who are of childbearing potential must be using acceptable forms of birth control.
- Capable of giving signed informed consent.
Exclusion
- History or presence of disorders capable of significantly altering the absorption, metabolism, or elimination of drugs.
- Abnormal blood pressure.
- Any malignancy within the past 5 years except certain localized malignancies, or breast cancer within the past 10 years.
- Has exclusionary psychiatric, hepatic, cardiovascular, gastrointestinal, respiratory, endocrine, neurological, hematological, or renal condition.
- Current or chronic history of liver disease or known hepatic or biliary abnormalities.
- Participants with exclusionary electrocardiogram findings.
- Past or intended use of exclusionary medications or vaccines.
- Exposure \> 4 new investigational products within 12 months, previous participation in this study, or current enrolment or participation in another investigational study.
- ALT \>1.5x upper limit of normal (ULN), total bilirubin \>1.5x ULN, and/or estimated serum creatinine clearance \<60 mL/min.
- History of or current infection with hepatitis B or hepatitis C.
- Positive SARS-CoV-2 test, having signs and symptoms suggestive of COVID-19, or contact with known COVID-19 positive person.
- Positive HIV antibody test.
- Participants with positive results for illicit drug use, regular use of drugs of abuse, tobacco or nicotine-containing product use, and/or excessive alcohol use.
Key Trial Info
Start Date :
December 18 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 3 2024
Estimated Enrollment :
46 Patients enrolled
Trial Details
Trial ID
NCT06168318
Start Date
December 18 2023
End Date
June 3 2024
Last Update
August 2 2024
Active Locations (1)
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1
GSK Investigational Site
Nottingham, United Kingdom, NG11 6JS