A Study to Investigate Pharmacokinetics, Safety and Tolerability of Long-Acting Cabotegravir Plus Recombinant Human Hyaluronidase PH20 in Healthy Adult Participants

Sponsor

ViiV Healthcare (Industry)

Overall Status

Recruiting

CT.gov ID

NCT05418868

Collaborator

(none)

Enrollment

Location

Arms

23.1

Anticipated Duration (Months)

2.6

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This is an open-label, dose-escalation study to investigate the safety, tolerability, and pharmacokinetics (PK) of single subcutaneous (SC) administration of long acting (LA) CAB200 or CAB400 with Recombinant Human Hyaluronidase PH20 (rHuPH20) (Parts A or B respectively).

Condition or Disease	Intervention/Treatment	Phase
HIV Infections	Drug: Cabotegravir 200 mg/mL Drug: Cabotegravir 400 mg/mL Drug: Recombinant human hyaluronidase PH20 (rHuPH20)	Phase 1

Study Design

Study Type:

Interventional

Anticipated Enrollment :

60 participants

Allocation:

Non-Randomized

Intervention Model:

Sequential Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Phase I, Multi-centre, Open-label, Single Dose Escalation Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Long-acting Cabotegravir Co-administered With Recombinant Human Hyaluronidase PH20 (rHuPH20) in Healthy Adult Volunteers

Actual Study Start Date :

Jun 14, 2022

Anticipated Primary Completion Date :

Jan 2, 2024

Anticipated Study Completion Date :

May 17, 2024

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Part A: CAB 200 mg/mL with rHuPH20	Drug: Cabotegravir 200 mg/mL CAB 200 milligram per milliliter (mg/mL) will be administered. Drug: Recombinant human hyaluronidase PH20 (rHuPH20) rHuPH20 will be administered.
Experimental: Part B: CAB 400 mg/mL with rHuPH20	Drug: Cabotegravir 400 mg/mL CAB 400 mg/mL will be administered. Drug: Recombinant human hyaluronidase PH20 (rHuPH20) rHuPH20 will be administered.

Arm

Intervention/Treatment

Experimental: Part A: CAB 200 mg/mL with rHuPH20

Drug: Cabotegravir 200 mg/mL

CAB 200 milligram per milliliter (mg/mL) will be administered.

Drug: Recombinant human hyaluronidase PH20 (rHuPH20)

rHuPH20 will be administered.

Experimental: Part B: CAB 400 mg/mL with rHuPH20

Drug: Cabotegravir 400 mg/mL

CAB 400 mg/mL will be administered.

Drug: Recombinant human hyaluronidase PH20 (rHuPH20)

rHuPH20 will be administered.

Outcome Measures

Primary Outcome Measures

Maximum observed plasma concentration (Cmax) of Cabotegravir [Up to Week 52]
Time of maximum observed plasma concentration (tmax) of Cabotegravir [Up to Week 52]
Area under the concentration - time curve from time zero to infinity [AUC(0-inf)] of Cabotegravir [Up to Week 52]
Area under the concentration - time curve from time zero to time of last quantifiable concentration or 4 weeks following the injection whichever is earlier [AUC(0-t)] of Cabotegravir [Up to Week 52]
Plasma Concentration of Cabotegravir at Week 4 [Week 4]
Plasma Concentration of Cabotegravir at Week 8 [Week 8]
Plasma Concentration of Cabotegravir at Week 12 [Week 12]
Plasma Concentration of Cabotegravir at Week 24 [Week 24]
Apparent terminal phase half-life (t1/2) of Cabotegravir [Up to Week 52]
Apparent long-acting absorption rate constant (KA-LA) of Cabotegravir [Up to Week 52]
Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs) [Up to Week 52]
Number of Participants with AEs by Severity [Up to Week 52]
Absolute value of Haematology parameter: Platelet count (cells per microliter) [Up to Week 52]
Absolute values of Haematology parameters: Hematocrit and Reticulocytes (percentage) [Up to Week 52]
Absolute values of Haematology parameters: Haemoglobin (Hgb), albumin and total protein (grams per deciliter) [Up to Week 52]
Absolute value of Haematology parameter: Red Blood Cell Count (RBC) (million cells per microliter) [Up to Week 52]
Absolute value of Haematology parameter: Mean Corpuscle Volume (MCV) (cubic microns) [Up to Week 52]
Absolute value of Haematology parameter: Mean Corpuscle Hemoglobin (MCH) (picograms per cell) [Up to Week 52]
Absolute values of Haematology parameters: Differential count of Neutrophils, Lymphocytes, Monocytes, Eosinophils, Basophils (percentage) [Up to Week 52]
Absolute values of Clinical Chemistry parameters: Glucose (fasting), Blood Urea Nitrogen (BUN), Creatinine, Direct Bilirubin and Total Bilirubin (milligrams per deciliter) [Up to Week 52]
Absolute values of Clinical Chemistry parameters: Sodium, Potassium, and Calcium (milliequivalents per liter) [Up to Week 52]
Absolute values of Clinical Chemistry parameters: AST/SGOT, ALT/ SGPT, ALP and CPK (International Units per liter) [Up to Week 52]
Clinical chemistry parameters such as Aspartate Aminotransferase (AST) / Serum Glutamic-Oxaloacetic Transaminase (SGOT), Alanine Aminotransferase (ALT)/ Serum Glutamic-Pyruvic Transaminase and (SGPT), Alkaline phosphatase (ALP) and Creatinine Phosphokinase (CPK) will be analyzed.
Absolute values of Coagulation parameters: Prothrombin time (PT) and Partial thromboplastin time (PTT) [Up to Week 52]
Absolute value of Coagulation parameter: International normalized ratio (INR) [Up to Week 52]
Change from Baseline in Haematology parameter: Platelet count (cells per microliter) [Baseline (Day 1) and up to Week 52]
Change from Baseline in Haematology parameters: Hematocrit and Reticulocytes (percentage) [Baseline (Day 1) and up to Week 52]
Change from Baseline in Haematology parameters: Hgb, albumin and total protein (grams per deciliter) [Baseline (Day 1) and up to Week 52]
Change from Baseline in Haematology parameter: RBC Count (million cells per microliter) [Baseline (Day 1) and up to Week 52]
Change from Baseline in Haematology parameter: MCV (cubic microns) [Baseline (Day 1) and up to Week 52]
Change from Baseline in Haematology parameter: MCH (picograms per cell) [Baseline (Day 1) and up to Week 52]
Change from Baseline in Haematology parameters: Differential count of Neutrophils, Lymphocytes, Monocytes, Eosinophils, Basophils (percentage) [Baseline (Day 1) and up to Week 52]
Change from Baseline in Clinical Chemistry parameters: Glucose (fasting), BUN, Creatinine, Direct Bilirubin and Total Bilirubin (milligrams per deciliter) [Baseline (Day 1) and up to Week 52]
Change from Baseline in Clinical Chemistry parameters: Sodium, Potassium, and Calcium (milliequivalents per liter) [Baseline (Day 1) and up to Week 52]
Change from Baseline in Clinical Chemistry parameters: AST/SGOT, ALT/ SGPT, ALP and CPK (International Units per liter) [Baseline (Day 1) and up to Week 52]
Change from Baseline in Coagulation parameters: PT and PTT [Baseline (Day 1) and up to Week 52]
Change from Baseline in Coagulation parameters: INR [Baseline (Day 1) and up to Week 52]
Number of participants with maximum toxicity grades increase from Baseline in haematology, clinical chemistry and coagulation parameters [Up to Week 52]

Secondary Outcome Measures

Dose proportionality of Cabotegravir based on AUC(0-inf) [Up to Week 52]
Dose proportionality of Cabotegravir based on AUC(0-t) [Up to Week 52]
Dose proportionality of Cabotegravir based on Cmax [Up to Week 52]
Dose proportionality of Cabotegravir based on plasma concentration [Week 4, 8, 12 and 24]
Number of participants with maximum post-baseline QTc values compared to baseline by category (to <=450 milliseconds (msec) or no change, to >450 msec to <=480 msec, to >480 msec to <=500 msec, and to >500 msec) [Up to Week 52]
Number of participants with maximum post-baseline increase in QTc values compared to baseline based on category (increase <=30 msec, increase of 31-60 msec, and increase of >60 msec) [Up to Week 52]
Number of participants with worst case post-baseline values relative to potential clinical importance criteria compared to baseline for diastolic blood pressure (DBP), systolic blood pressure (SBP) and pulse rate [Up to Week 52]
Number of participants with worst case post-baseline values relative to potential clinical importance criteria compared to baseline will be categorized into change to low, change to within range or no change, and change to high.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 55 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

At the time of obtaining informed consent, participants age should be equal to or greater than (=>)18 years and equal to or less than (=<) 55 years.
Participants who are overtly healthy as determined by medical evaluation including medical history, physical examination, laboratory tests, and cardiac monitoring.
Body weight =>40 kilogram (kg) and body mass index (BMI) within the range =>18 to =<32 kilogram per meter square (kg/m^2).
Participants who are negative on two (2) consecutive tests for SARS-CoV-2, one performed prior to admission to the Phase 1 unit (up to Day 7 prior to admission) and one prior to dosing, i.e., on Day -1 or Day 1.
Contraceptive use by men and women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.
Capable of giving written informed consent.

Exclusion Criteria:

Current presence or history of cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, haematological, or neurological disorders.
Current or chronic history of liver disease or known hepatic or biliary abnormalities.
History of ongoing or clinically relevant seizure disorder within the previous 2 years, including participants who have required treatment for seizures within this time period.
Signs and symptoms which, in the opinion of the investigator, are suggestive of COVID-19 (e.g., fever, cough) within 14 days prior to screening; and/or contact with known COVID-19 positive person(s) in the 14 days prior to screening.
Human immunodeficiency virus (HIV-1 or HIV-2) infection as indicated by positive antibody/antigen test.
History of or on-going high-risk behaviours that, in the opinion of the investigator, may put the participant at increased risk for HIV infection including, but not limited to, participants in HIV discordant relationships, or men who report current or prior unprotected anal sex with other men and those reporting prior or current injecting drug use.
Presence of hepatitis B surface antigen (HBsAg), or positive hepatitis C antibody test result at screening or within 3 months prior to first dose of study treatment.
Abnormal blood pressure.
Evidence of previous myocardial infarction.
Any conduction abnormality (including but not specific to left or right complete bundle branch block, atrioventricular [AV] block [2nd degree or higher], Wolff- Parkinson-White [WPW] syndrome).
Any significant arrhythmia which, in the opinion of the investigator or the medical monitor, will interfere with the safety for the individual participant.
One or more exclusionary values for a screening Electrocardiogram (ECG).
Alanine transaminase (ALT) >1.5x upper limit of normal (ULN).
Bilirubin >1.5xULN (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35%).
Estimated Glomerular Filtration Rate (eGFR) <60 milliliter per minute (mL/min) using the CKD-EPI Creatinine Equation (2021).
Haemoglobin <12.5 gram per deciliter (g/dL) for men and <11 g/dL for women.
Positive pre-study drug/alcohol screen.
Regular use of tobacco- or nicotine-containing products within 3 months prior to screening; or urinary cotinine levels indicative of smoking or history or regular use of tobacco- or nicotine-containing products (e.g., nicotine patches or vaporizing devices).
Regular alcohol consumption within 6 months prior to the study defined as an average weekly intake of >14 units for males or >7 units for females.
Regular use of known drugs of abuse.
Concurrent participation in another clinical trial (except imaging trials); or has participated in a clinical trial and received an investigational product within the following time period prior to the first dosing day in this study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer).
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 four (4) new chemical entities within 12 months prior to the first dosing day.
History of sensitivity to any of the study interventions (or components thereof), a history of drug allergy or other allergy that, in the opinion of the investigator or medical monitor, contraindicates their participation, including a known hypersensitivity to hyaluronidases.
Current or anticipated need for chronic anti-coagulation therapy.
Hereditary coagulation and platelet disorders (e.g., haemophilia or Von Willebrand disease [VWD]).
Participant has a tattoo overlying the location of injection or an underlying skin disease or condition (e.g., infection, inflammation, dermatitis, eczema, drug rash, drug allergy, psoriasis, food allergy, urticaria) that, in the opinion of the investigator, may interfere with interpretation of injection site reactions or administration of study intervention.
Any other clinical condition, behavior or prior therapy that, in the opinion of the investigator, would make the participant unsuitable for the study; unable to comply with dosing requirements; or unable to comply with study visits.