A Study to Investigate Safety, Tolerability, and Pharmacokinetics (PK) of VH4524184 and the Potential for Changes in Cytochrome P450 3A (CYP3A) Activity

Sponsor

ViiV Healthcare (Industry)

Overall Status

Recruiting

CT.gov ID

NCT05631704

Collaborator

(none)

105

Enrollment

Location

Arms

8.9

Anticipated Duration (Months)

11.7

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This study is designed to investigate the safety, tolerability and PK of VH4524184 (GSK4524184) and the potential of VH4524184 to inhibit or induce CYP3A activity in healthy participants.

Condition or Disease	Intervention/Treatment	Phase
HIV Infections	Drug: VH4524184 Drug: Midazolam Drug: Placebo	Phase 1

Study Design

Study Type:

Interventional

Anticipated Enrollment :

105 participants

Allocation:

Randomized

Intervention Model:

Sequential Assignment

Intervention Model Description:

Participants will receive escalating doses of VH4524184 or placebo in Part 1 and Part 2 of the study. In Part 3, participants will receive VH4524184 under fasted and fed conditions.Participants will receive escalating doses of VH4524184 or placebo in Part 1 and Part 2 of the study. In Part 3, participants will receive VH4524184 under fasted and fed conditions.

Masking:

Double (Participant, Investigator)

Masking Description:

This will be a double blind study.

Primary Purpose:

Treatment

Official Title:

A Phase 1 Double-Blind (Sponsor-unblinded), Placebo-Controlled Randomized, Single and Multiple Ascending Dose First-Time-in-Human Study to Investigate the Safety, Tolerability, and Pharmacokinetics of VH4524184 and the Potential for Changes in Cytochrome P450 3A (CYP3A) Activity

Actual Study Start Date :

Dec 2, 2022

Anticipated Primary Completion Date :

Aug 31, 2023

Anticipated Study Completion Date :

Aug 31, 2023

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Part 1: Cohort 1: Participants receiving VH4524184 DL1 Eligible participants will receive VH4524184 Dose Level 1 (DL1) during Cohort 1 of Part 1 of the study.	Drug: VH4524184 VH4524184 will be administered.
Placebo Comparator: Part 1: Cohort 1: Participants receiving Placebo Eligible participants will receive Placebo matching VH4524184 DL1 during Cohort 1 of Part 1 of the study.	Drug: Placebo Placebo will be administered.
Experimental: Part 1: Cohort 2: Participants receiving VH4524184 DL2 Eligible participants will receive VH4524184 DL2 during Cohort 2 of Part 1 of the study.	Drug: VH4524184 VH4524184 will be administered.
Placebo Comparator: Part 1: Cohort 2: Participants receiving Placebo Eligible participants will receive Placebo matching VH4524184 DL2 during Cohort 2 of Part 1 of the study.	Drug: Placebo Placebo will be administered.
Experimental: Part 1: Cohort 3: Participants receiving VH4524184 DL3 Eligible participants will receive VH4524184 DL3 during Cohort 3 of Part 1 of the study.	Drug: VH4524184 VH4524184 will be administered.
Placebo Comparator: Part 1: Cohort 3: Participants receiving Placebo Eligible participants will receive Placebo matching VH4524184 DL3 during Cohort 3 of Part 1 of the study.	Drug: Placebo Placebo will be administered.
Experimental: Part 1: Cohort 4: Participants receiving VH4524184 DL4 Eligible participants will receive VH4524184 DL4 during Cohort 4 of Part 1 of the study.	Drug: VH4524184 VH4524184 will be administered.
Placebo Comparator: Part 1: Cohort 4: Participants receiving Placebo Eligible participants will receive Placebo matching VH4524184 DL4 during Cohort 4 of Part 1 of the study.	Drug: Placebo Placebo will be administered.
Experimental: Part 1: Cohort 5: Participants receiving VH4524184 DL5 Eligible participants will receive VH4524184 DL5 during Cohort 5 (optional) of Part 1 of the study.	Drug: VH4524184 VH4524184 will be administered.
Placebo Comparator: Part 1: Cohort 5: Participants receiving Placebo Eligible participants will receive Placebo matching VH4524184 DL5 during Cohort 5 (optional) of Part 1 of the study.	Drug: Placebo Placebo will be administered.
Experimental: Part 1: Cohort 6: Participants receiving VH4524184 DL6 Eligible participants will receive VH4524184 DL6 during Cohort 6 (optional) of Part 1 of the study.	Drug: VH4524184 VH4524184 will be administered.
Placebo Comparator: Part 1: Cohort 6: Participants receiving Placebo Eligible participants will receive Placebo matching VH4524184 DL6 during Cohort 6 (optional) of Part 1 of the study.	Drug: Placebo Placebo will be administered.
Experimental: Part 2: Cohort 7: Participants receiving VH4524184 RL1 Eligible participants will receive VH4524184 Repeat dose Level 1 (RL1) during Cohort 7 (Part 2) of the study.	Drug: VH4524184 VH4524184 will be administered.
Placebo Comparator: Part 2: Cohort 7: Participants receiving Placebo Eligible participants will receive Placebo matching VH4524184 RL1 during Cohort 7 (Part 2) of the study.	Drug: Placebo Placebo will be administered.
Experimental: Part 2: Cohort 8: Participants receiving VH4524184 RL2 Eligible participants will receive VH4524184 RL2 during Cohort 8 (Part 2) of the study. If Cohort 8 is the highest Part 2 dose cohort, participants may also receive midazolam probe before and following repeat dose administration of VH4524184	Drug: VH4524184 VH4524184 will be administered. Drug: Midazolam Midazolam will be administered in the highest dose cohort in Part 2 (Cohorts 8 or 9).
Placebo Comparator: Part 2: Cohort 8: Participants receiving Placebo Eligible participants will receive Placebo matching VH4524184 RL2 during Cohort 8 (Part 2) of the study. If Cohort 8 is the highest Part 2 dose cohort, participants may also receive midazolam probe before and following repeat dose administration of Placebo matching VH4524184.	Drug: Midazolam Midazolam will be administered in the highest dose cohort in Part 2 (Cohorts 8 or 9). Drug: Placebo Placebo will be administered.
Experimental: Part 2: Cohort 9: Participants receiving VH4524184 RL3 Eligible participants will receive VH4524184 RL3 during Cohort 9 (Part 2) (optional) of the study. If Cohort 9 is the highest Part 2 dose cohort, participants may also receive midazolam probe before and following repeat dose administration of VH4524184.	Drug: VH4524184 VH4524184 will be administered. Drug: Midazolam Midazolam will be administered in the highest dose cohort in Part 2 (Cohorts 8 or 9).
Placebo Comparator: Part 2: Cohort 9: Participants receiving Placebo Eligible participants will receive Placebo matching VH4524184 RL3 during Cohort 9 (Part 2) (optional) of the study. If Cohort 9 is the highest Part 2 dose cohort, participants may also receive midazolam probe before and following repeat dose administration of Placebo matching VH4524184.	Drug: Midazolam Midazolam will be administered in the highest dose cohort in Part 2 (Cohorts 8 or 9). Drug: Placebo Placebo will be administered.
Experimental: Part 3: Cohort 10: VH4524184 Fasted/ VH4524184 Fed Eligible participants will receive VH4524184 under fasted condition in Treatment Period 1 followed by VH4524184 under fed condition in Treatment Period 2 during Cohort 10 (Part 3) of the study. Treatment Periods will be separated by a washout period.	Drug: VH4524184 VH4524184 will be administered.

Outcome Measures

Primary Outcome Measures

Part 1: Number of participants with serious adverse events (SAE) and non-serious adverse events (non-SAE) [Up to 4 weeks]
Part 2: Number of participants with SAE and non-SAE [Up to 6.5 weeks]
Part 3: Number of participants with SAE and non-SAE [Up to 6.5 weeks]
Part 1: Number of participants with adverse events based on severity [Up to 4 weeks]
Part 2: Number of participants with adverse events by severity [Up to 6.5 weeks]
Part 3: Number of participants with adverse events based on severity [Up to 6.5 weeks]
Part 1: Percentage of participants who discontinue treatment due to adverse events (AE) [Up to 4 weeks]
Part 2: Percentage of participants who discontinue treatment due to AE [Up to 6.5 weeks]
Part 3: Percentage of participants who discontinue treatment due to AE [Up to 6.5 weeks]
Part 1: Change from Baseline in Aspartate aminotransferase (AST), Alanine aminotransferase (ALT) and Alkaline phosphatase (ALP) (International units per liter) [Baseline (Day 1) and up to 4 weeks]
Part 2: Change from Baseline in AST, ALT and ALP (International units per liter) [Baseline (Day 1) and up to 6.5 weeks]
Part 3: Change from Baseline in AST, ALT and ALP (International units per liter) [Baseline (Day 1) and up to 6.5 weeks]
Part 1: Change from Baseline in Total bilirubin and Direct bilirubin (Micromoles per liter) [Baseline (Day 1) and up to 4 weeks]
Part 2: Change from Baseline in Total bilirubin and Direct bilirubin (Micromoles per liter) [Baseline (Day 1) and up to 6.5 weeks]
Part 3: Change from Baseline in Total bilirubin and Direct bilirubin (Micromoles per liter) [Baseline (Day 1) and up to 6.5 weeks]
Part 1: Change from Baseline in Prothrombin time and Partial Thromboplastin Time (Seconds) [Baseline (Day 1) and up to 4 weeks]
Part 2: Change from Baseline in Prothrombin time and Partial Thromboplastin Time (Seconds) [Baseline (Day 1) and up to 6.5 weeks]
Part 3: Change from Baseline in Prothrombin time and Partial Thromboplastin Time (Seconds) [Baseline (Day 1) and up to 6.5 weeks]
Part 1: Change from Baseline in International normalized ratio (INR) (Ratio) [Baseline (Day 1) and up to 4 weeks]
Part 2: Change from Baseline in INR (Ratio) [Baseline (Day 1) and up to 6.5 weeks]
Part 3: Change from Baseline in INR (Ratio) [Baseline (Day 1) and up to 6.5 weeks]
Part 1: Number of participants with maximum toxicity grade increase from Baseline in liver panel laboratory parameters; AST, ALT, ALP, Total bilirubin, Direct bilirubin, Prothrombin time, Partial Thromboplastin Time and INR [Baseline (Day 1) and up to 4 weeks]
Part 2: Number of participants with maximum toxicity grade increase from Baseline in liver panel laboratory parameters; AST, ALT, ALP, Total bilirubin, Direct bilirubin, Prothrombin time, Partial Thromboplastin Time and INR [Baseline (Day 1) and up to 6.5 weeks]
Part 3: Number of participant with maximum toxicity grade increase from Baseline in liver panel laboratory parameters; AST, ALT, ALP, Total bilirubin, Direct bilirubin, Prothrombin time, Partial Thromboplastin Time and INR [Baseline (Day 1) and up to 6.5 weeks]
Part 1: Area under the plasma-concentration time curve from zero (pre-dose) extrapolated to infinite time (AUC[0-infinity]) following dosing of VH4524184 [Up to 4 weeks]
Part 2: Area under the plasma concentration-time curve from zero (pre-dose) to the end of the dosing interval at steady state (AUC[0-tau]) following dosing of VH4524184 [Up to 6.5 weeks]
Part 1: Maximum observed plasma drug concentration (Cmax) following dosing of VH4524184 [Up to 4 weeks]
Part 2: Cmax following dosing of VH4524184 [Up to 6.5 weeks]
Part 1: Time to maximum observed plasma drug concentration (tmax) following dosing of VH4524184 [Up to 4 weeks]
Part 2: Tmax following dosing of VH4524184 [Up to 6.5 weeks]
Part 1: Apparent terminal half-life (t1/2) following dosing of VH4524184 [Up to 4 weeks]
Part 2: T1/2 following dosing of VH4524184 [Up to 6.5 weeks]

Secondary Outcome Measures

Part 1: Number of participants with treatment emergent Grade 3 or Grade 4 laboratory abnormalities [Up to 4 weeks]
Part 2: Number of participants with treatment emergent Grade 3 or Grade 4 laboratory abnormalities [Up to 6.5 weeks]
Part 3: Number of participants with treatment emergent Grade 3 or Grade 4 laboratory abnormalities [Up to 6.5 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 50 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Participant must be 18 to 50 years of age.
Participants who are overtly healthy.
Body weight >=50.0 kilograms (kg) (110 pounds [lbs]) for men and >=45.0 kg (99 lbs) for women and body mass index within the range 18.5 to 32.0 kilograms per meter square (kg/m^2) (inclusive).
Male or female. Male Participants: No contraceptive restrictions for male participants. Female Participants: A female participant (female sex assigned at birth) is eligible to participate if she is not pregnant, or breastfeeding and is not physically able to have a baby.

Exclusion Criteria:

History or presence of clinical condition that could significantly alter how medicines are absorbed, broken down or eliminated from the body; be risky to the participant, or make it difficult to interpret the data from the study.
Pre-existing clinically relevant gastro-intestinal disorders.
Abnormal blood pressure.
Certain blood or other cancers within the past 5 years.
Breast cancer within the past 10 years
Current or chronic history of liver disease or liver or bile tract abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).
QT interval corrected for heart rate according to Fridericia's formula (QTcF) >450 milliseconds (msec).
Medical history of cardiac arrhythmias or cardiac disease or a family and personal history of long QT syndrome.
History of seizure
Any known or suspected pre-existing psychiatric condition, including depression, anxiety and insomnia/sleep disturbances.
Any positive (abnormal) response to the Columbia Suicide Severity Rating Scale (CSSRS).
Past or intended use of over-the-counter or prescription medication within 7 days (or 14 days if the drug is a potential enzyme inducer) or 5 half-lives (whichever is longer) prior to dosing and for the duration of the study.
Receipt of any live vaccine(s) or vaccines against Coronavirus disease 2019 (Covid-19) within 28 days prior to screening or plans to receive such vaccines during the study.
Exposure to more than 4 new investigational products (including long-acting investigational products) within 12 months prior to the first dosing day.
Current enrollment or past participation in another investigational study in which an investigational intervention (e.g., drug, human blood product, monoclonal antibody, vaccine, invasive device) was administered within the last 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer) before signing of consent (OR screening) any other clinical study.
Participation in the study would result in loss of blood or blood products in excess of 500 milliliters (mL) over a 56-day period.
Current enrollment or past participation in this clinical study.
Estimated Glomerular Filtration Rate (eGFR) <90 milliliters per minute (mL/min) (calculated using Chronic Kidney Disease Epidemiology Collaboration equation) or serum creatinine >1.1 times Upper limit of normal (ULN).
Hemoglobin <12.5 grams per deciliter (g/dL) for men and <11 g/dL for women
ALT or AST >1.5 times ULN
Total bilirubin >1.5 times ULN (isolated bilirubin >1.5 times ULN is acceptable if bilirubin is fractionated and direct bilirubin <35 percent [%]).
Any significant arrhythmia or Electrocardiogram (ECG) finding
Exclusion criteria for Screening ECG (a single repeat is allowed for eligibility determination): Heart rate:<45 or >100 beats per minute (bpm) (Males), <50 or >100 bpm (Females); PR interval: <120 or >220 msec; QRS duration: <70 or >120 msec and QTcF interval: >450 msec.
Presence of hepatitis B surface antigen (HBsAg) at screening.
Positive Hepatitis C antibody test result at screening
Positive pre-study drug/alcohol screen.
Positive human immunodeficiency virus (HIV) antibody test.
Regular alcohol consumption within 6 months prior to the study
Regular use of known drugs of abuse
Urinary cotinine levels indicative of smoking or history or regular use of tobacco- or nicotine-containing products within 6 months prior to screening and at admission.
Sensitivity to the study drug, or components thereof, midazolam (For Part 2, midazolam probe cohort), excipients contained therein, benzodiazepines, or other drug or other allergy that, in the opinion of the investigator or Sponsor Medical Monitor, contraindicates participation in the study.