Dolutegravir Pediatric Liquid Formulation Study

HIV Infections Clinical Trial

Official title:

Non-randomized, Sequential, Fixed-sequence Evaluation of Prototype Dolutegravir Liquid Formulations Versus 5mg Dolutegravir Dispersible Tablets Following Single-dose Fasted-state Administrations to Normal Healthy Adult Participants

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03921723
• Other study ID #: 209354
• Status: Completed
• Phase: Phase 1
• Start date: May 7, 2019
• Est. completion date: July 25, 2019

Study information

• Verified date: July 2020
• Source: ViiV Healthcare
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is an open-label, single-center, single dose, non-randomized, sequential, fixed-sequence study, which will evaluate pharmacokinetics (PK) of dolutegravir (DTG) in healthy adult subjects. The study will contain 6 periods with five prototype liquid formulations for evaluation in fasted state. In period 1, 2 and 3 single reference dose of 2 dispersible tablets of 5 milligram DTG will be administered and at least 2 liquid prototype DTG formulations (containing a target total dose of 10mg DTG). There will be a wash-out period of 7 days between each period. In period 4 through 6, there would be options to evaluate additional prototype liquid formulations. The total duration of study will be up to 17 weeks. DTG has been found to be safe and effective in adults infected with human immunodeficiency virus (HIV). DTG dispersible tablets have been developed primarily for use in children from 4 weeks to 6 years of age, and a DTG liquid formulation are is being developed to study the appropriate dose needed for the HIV-exposed and infected neonatal population in the first four weeks of life. Approximately 18 subjects will be enrolled in this study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 22
• Est. completion date: July 25, 2019
• Est. primary completion date: July 25, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Subject must be 18 to 55 years of age inclusive, at the time of signing the informed consent.

• Subjects who are overtly healthy as determined by medical evaluation including medical history, physical examination, laboratory tests, and cardiac evaluation.

• Body weight >= 50 kg (110 pounds [lbs]) for men and >=45 kg (99 lbs) for women and body mass index (BMI) within the range 18.5-31.0 kilogram per meter square (kg/m^2) (inclusive).

• Male and female subjects will be part of study. A female subject is eligible to participate if she is not pregnant or breastfeeding, and is not a woman of childbearing potential (WOCBP).

• Additional requirements for pregnancy testing, if needed, during and after study intervention; The investigator is responsible for review of medical history, menstrual history, and recent sexual activity to decrease the risk for inclusion of a woman with an early undetected pregnancy.

• Subject should be capable of giving signed informed consent as which includes compliance with the requirements and restrictions listed in the informed consent form (ICF).

Exclusion Criteria:

• History or presence of cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, hematological, or neurological disorders capable of significantly altering the absorption, metabolism, or elimination of drugs; constituting a risk when taking the study intervention; or interfering with the interpretation of data.

• Abnormal blood pressure as determined by the investigator.

• Alanine transaminase (ALT) >1.5 times upper limit of normal (ULN).

• Bilirubin >1.5times ULN (isolated bilirubin >1.5 times ULN is acceptable if bilirubin is fractionated and direct bilirubin <35%).

• Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).

• QT correction using Fridericia Formula (QTcF) >450 millisecond (msec)

• Past or intended use of over-the-counter or prescription medication (including herbal medications) within 7 days prior to dosing. Paracetamol.

• History of allergy or sensitivity to DTG.

• Participation in the study would result in loss of blood or blood products in excess of 500 mL within 56 days.

• Exposure to more than 4 new chemical entities within 12 months prior to the first dosing day.

• Current enrollment or past participation within the last 30 days before signing of consent in this or any other clinical study involving an investigational study intervention or any other type of medical research.

• Presence of Hepatitis B surface antigen (HBsAg), or a positive hepatitis B core antibody with a negative hepatitis B surface antibody at screening.

• Positive Hepatitis C antibody test result at screening: Subjects with positive Hepatitis C antibody due to prior resolved disease can be enrolled, only if a confirmatory negative Hepatitis C ribonucleic acid (RNA) test is obtained.

• Positive Hepatitis C RNA test result at screening or within 3 months prior to first dose of study intervention.

• Positive pre-study drug/alcohol screen.

• Positive HIV antibody test.

• Regular use of known drugs of abuse.

• Regular alcohol consumption within one month prior to the study defined as: For the United Kingdom an average weekly intake of >14 units for males or females. One unit is equivalent to 8 gram (g) of alcohol: a half-pint (~240 mL) of beer, 1 glass (125 mL) of wine or 1 (25 mL) measure of spirits.

• Urinary cotinine levels indicative of smoking or history or regular use of tobacco- or nicotine-containing products (e.g. nicotine patches or vaporizing devices) within 6 months prior to screening.

Related Conditions & MeSH terms

• HIV Infections

Intervention

Drug:
• Dolutegravir dispersible tablet
DTG will be available as an oral tablet with dosing strength of 5 mg 2 tablet will be dispersed in water will be administered orally for prescribed regimen.
• Dolutegravir oral suspension
DTG will be available as an oral suspension with dosing strength of 5 mg per milliliter (ml) or 2 mg per ml with miglyol 812N or ethyl cellulose in miglyol 812N as vehicle for suspension administered orally for prescribed regimen.
• Dolutegravir oral solution
DTG will be available as an oral solution with dosing strength of 2 mg per ml will be administered orally for prescribed regimen.

Locations

Country	Name	City	State
United Kingdom	GSK Investigational Site	Nottingham

Sponsors (1)

Lead Sponsor	Collaborator
ViiV Healthcare

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Area Under the Plasma Concentration Time Curve From Time Zero to the Last Quantifiable Time Point (AUC[0-t]) for DTG	Blood samples were collected at indicated time points and pharmacokinetic (PK) analysis was performed. PK parameters were determined by non-compartmental methods.	Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3,3.5, 4, 5, 6, 8, 12, 16, 24, 48, and 72 hours post-dose
Primary	AUC From Time Zero to Infinity (AUC[0-inf]) for DTG	Blood samples were collected at indicated time points and PK analysis was performed. PK parameters were determined by non-compartmental methods.	Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3,3.5, 4, 5, 6, 8, 12, 16, 24, 48, and 72 hours post-dose
Primary	Maximum Observed Concentration (Cmax) for DTG	Blood samples were collected at indicated time points and PK analysis was performed. PK parameters were determined by non-compartmental methods.	Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3,3.5, 4, 5, 6, 8, 12, 16, 24, 48, and 72 hours post-dose
Secondary	Absorption Lag Time (Tlag) Following Administration of DTG	Blood samples were collected at indicated time points and PK analysis was performed. PK parameters were determined by non-compartmental methods.	Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3,3.5, 4, 5, 6, 8, 12, 16, 24, 48, and 72 hours post-dose
Secondary	Time of Maximum Observed Concentration (Tmax) Following Administration of DTG	Blood samples were collected at indicated time points and PK analysis was performed. PK parameters were determined by non-compartmental methods.	Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 16, 24, 48, and 72 hours post-dose
Secondary	Time of Last Quantifiable Concentration (Tlast) Following Administration of DTG	Blood samples were collected at indicated time points and PK analysis was performed. PK parameters were determined by non-compartmental methods.	Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 16, 24, 48, and 72 hours post-dose
Secondary	Elimination Half-life (t½) Following Administration of DTG	Blood samples were collected at indicated time points and PK analysis was performed. PK parameters were determined by non-compartmental methods.	Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3,3.5, 4, 5, 6, 8, 12, 16, 24, 48, and 72 hours post-dose
Secondary	Apparent Elimination Rate Constant (Lambda z) Following Administration of DTG	Blood samples were collected at indicated time points and PK analysis was performed. PK parameters were determined by non-compartmental methods.	Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 16, 24, 48, and 72 hours post-dose
Secondary	Percentage of AUC(0-inf) Extrapolated (%AUCex) Following Administration of DTG	Blood samples were collected at indicated time points and PK analysis was performed. PK parameters were determined by non-compartmental methods.	Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3,3.5, 4, 5, 6, 8, 12, 16, 24, 48, and 72 hours post-dose
Secondary	AUC From Time Zero to 24 Hours (AUC[0-24]) Following Administration of DTG	Blood samples were collected at indicated time points and PK analysis was performed. PK parameters were determined by non-compartmental methods.	Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3,3.5, 4, 5, 6, 8, 12, 16, and 24 hours post-dose
Secondary	AUC From Time Zero to 72 Hours (AUC[0-72]) Following Administration of DTG	Blood samples were collected at indicated time points and PK analysis was performed. PK parameters were determined by non-compartmental methods.	Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 16, 24, 48 and 72 hours post-dose
Secondary	Apparent Oral Clearance (CL/F) Following Administration of DTG	Blood samples were collected at indicated time points and PK analysis was performed. PK parameters were determined by non-compartmental methods.	Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3,3.5, 4, 5, 6, 8, 12, 16, 24, 48 and 72 hours post-dose
Secondary	Last Quantifiable Concentration (Ct) Following Administration of DTG	Blood samples were collected at indicated time points and PK analysis was performed. PK parameters were determined by non-compartmental methods.	Pre-dose and 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3,3.5, 4, 5, 6, 8, 12, 16, 24, 48 and 72 hours post-dose
Secondary	Apparent Oral Volume of Distribution (Vz/F) Following Administration of DTG	Blood samples were collected at indicated time points and PK analysis was performed. PK parameters were determined by non-compartmental methods.	Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3,3.5, 4, 5, 6, 8, 12, 16, 24, 48 and 72 hours post-dose
Secondary	Concentration at 24hours Post-dose (C24) Following Administration of DTG	Blood samples were collected at indicated time points and PK analysis was performed. PK parameters were determined by non-compartmental methods.	24 hours
Secondary	Change From Baseline in Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP)	SBP and DBP was measured in a supine position after at least 5 minutes of rest for the participant in a quiet setting without any distractions using a completely automated device. Day -1 was considered as Baseline. Change from Baseline was calculated by subtracting Baseline value from the specific time point value.	Baseline (Day -1) and Day 4
Secondary	Change From Baseline in Pulse Rate	Pulse rate was measured in a supine position after at least 5 minutes of rest for the participant in a quiet setting without any distractions using a completely automated device. Day -1 was considered as Baseline. Change from Baseline was calculated by subtracting Baseline value from the specific time point value.	Baseline (Day -1) and Day 4
Secondary	Number of Participants With Non-serious Adverse Events (AEs) and Serious Adverse Events (SAEs)	An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study intervention, whether or not considered related to the study intervention. A SAE is defined as any untoward medical occurrence that, at any dose results in death,is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent disability/incapacity, is a congenital anomaly/birth defect, any other situation according to medical or scientific judgement.	Up to Week 11
Secondary	Number of Participants With Clinically Significant Hematology Parameters	Blood samples were collected to analyze the following hematology parameters: Basophils, Eosinophils, Lymphocytes, Monocytes, Neutrophils, Platelets, hemoglobin, hematocrit, mean corpuscular hemoglobin (MCH), mean corpuscular volume (MCV), percentage reticulocytes and red blood cell count. Data for clinically significant abnormal hematology parameters have been presented. Clinically significant abnormal laboratory findings are those which are not associated with the underlying disease, unless judged by the investigator to be more severe than expected for the participant's condition.	Baseline (Day -1)
Secondary	Number of Participants With Clinically Significant Chemistry Parameters	Blood samples were collected to analyze the following clinical chemistry parameters: Potassium, calcium, sodium, creatinine, glucose, alkaline phosphatase, Aspartate Aminotransferase (AST), Alanine Aminotransferase (ALT), Blood urea nitrogen (BUN), total and direct bilirubin, total protein and creatine kinase. Data for clinically significant abnormal clinical chemistry parameters have been presented. Clinically significant abnormal laboratory findings are those which are not associated with the underlying disease, unless judged by the investigator to be more severe than expected for the participant's condition.	Baseline (Day -1)
Secondary	Number of Participants With Clinically Significant Urine Parameters	Urine samples were collected to analyze the following urinalysis parameters: specific gravity, potential of hydrogen (pH). Clinically significant abnormal laboratory findings are those which are not associated with the underlying disease, unless judged by the investigator to be more severe than expected for the participant's condition.	Baseline (Day -1)