Safety and Acceptability of Cabotegravir in HIV Uninfected Women in KwaZulu-Natal, South Africa (CAPRISA014)

Phase II Trial to Assess the Safety and Acceptability of the Long-acting Injectable HIV Integrase Inhibitor, Cabotegravir (GSK1265744), in HIV Uninfected Women in KwaZulu-Natal, South Africa

The CAPRISA 014 trial aims to assess the safety and acceptability of the long-acting (LA) injectable antiretroviral agent, cabotegravir LA (GSK1265744), in HIV uninfected women in KwaZulu-Natal, South Africa.

Study Overview

• Status: Withdrawn
• Conditions: Human Immunodeficiency Virus
• Intervention / Treatment: Drug: cabotegravir; Drug: Placebo

Detailed Description

The CAPRISA 014 trial is designed to establish the safety and acceptability of cabotegravir LA in sexually active, at-risk HIV-uninfected women. A total of 632 HIV uninfected women (18 to 30 years) from two sites in KwaZulu-Natal, South Africa will be enrolled. The trial will be approximately 24 months, with an additional 12 months post-trial safety observation. The study is divided into three periods:

Period 1 - Clinical trial oral lead-in (up to 34 days) - Consenting participants will be randomized to receive daily oral cabotegravir (30mg tablets) or daily oral placebo for approximately 30 days, to assess safety and tolerability prior to exposure to the LA injectable formulation.

Period 2 - Clinical trial follow-up with injectable (approximately 48-96 weeks) - Participants who have successfully completed Period 1 will receive intra-muscular (IM) gluteal injections of cabotegravir LA (800 mg, administered as two 400 mg injections) or placebo every 12 weeks. The end of Period 2 marks the completion of clinical trial follow-up.

Period 3 - Post-trial safety follow-up off-product (approximately 12 months) - During this post-trial safety observation period, participants will be followed up (off product) for approximately 12 months after completion of period 2.

• Study Type: Interventional
• Phase: Phase 2

Contacts and Locations

Study Locations

• South Africa
  • KwaZulu-Natal
    • Durban, KwaZulu-Natal, South Africa, 4001
      • CAPRISA eThekwini Research Clinic
    • Mafakatini, KwaZulu-Natal, South Africa, 3290
      • CAPRISA Vulindlela Research Clinic

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 30 years (Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: Female

Description

Inclusion Criteria:

• Able and willing to provide written informed consent to be screened for, and to enrol in, the study.
• Able and willing to provide adequate locator information for study retention purposes.
• Sexually active, defined as having had vaginal intercourse at least once in the past 30 days prior to screening.
• HIV negative on testing performed by study staff
• Have a negative pregnancy test performed by study staff
• Agree to use a non-barrier form of contraceptive
• Agree to adhere to study visits and procedures.
• Haemoglobin > 11 g/dL,
• ALT < ULN
• AST < ULN
• Total bilirubin < Grade 1
• Direct bilirubin < ULN
• Creatinine clearance ≥60 mL/min
• Hepatitis B surface antigen (HBsAg) negative
• Hepatitis C Ab negative
• In general good health, as assessed clinically

Exclusion Criteria:

• Past or current participation in any other HIV interventional research study or other concurrent studies which may interfere with this study.
• Clinically significant cardiovascular disease, including:
• ECG with:
• heart rate <50 or >100 beats per minute (one repeat ECG is allowed during screening; can be performed on the same day)
• QRS duration >120 msec
• QTc interval (B or F) > 450 msec
• evidence of previous myocardial infarction (pathologic Q waves, S-T segment changes (except early repolarization)
• any conduction abnormality (including but not specific to left or right complete bundle branch block, Atrioventricular block [2nd degree (type II) or higher], Wolf Parkinson White syndrome)
• sinus pauses > 3 seconds
• any significant arrhythmia which, in the opinion of the Principal Investigator or designee, will interfere with the safety for the individual participant
• history of non-sustained (3 consecutive ventricular ectopic beats on ECG at screening or entry) or sustained ventricular tachycardia
• History/evidence of symptomatic arrhythmia, angina/ischemia, coronary artery bypass grafting surgery or percutaneous transluminal coronary angioplasty or any clinically significant cardiac disease
• Underlying skin disease or currently active skin disorder (e.g., infection, inflammation, dermatitis, eczema, psoriasis, urticaria). Mild cases of localized disease or other mild skin condition may not be exclusionary at the discretion of the Principal Investigator or designee.
• Has a tattoo or other dermatological condition overlying the buttock region which in the opinion of the Principal Investigator or designee, may interfere with interpretation of injection site reactions.
• History of acute or chronic liver disease (e.g., non-alcoholic or alcoholic steatohepatitis) or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome, asymptomatic gallstones, or cholecystectomy).
• Coagulopathy (primary or iatrogenic) which would contraindicate IM injection.
• Active or planned use of prohibited medications as described in the SSP manual (updated regularly from the Investigator's Brochure).
• Pregnant or currently breastfeeding, or intends to become pregnant and/or breastfeed during the study.
• Known Hypersensitivity to egg, soya or peanut protein.
• Has any other condition that, based on the opinion of the Principal Investigator or designee, would preclude provision of informed consent, make participation in the study unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Prevention
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Cabotegravir; Women randomised to the cabotegravir arm will receive daily oral cabotegravir (30 mg tablets) for approximately 30 days and thereafter will receive intra-muscular gluteal injections of cabotegravir LA (800 mg, administered as two 400 mg injections) every 12 weeks	Drug: cabotegravir; Cabotegravir 30 mg tablets are formulated as white to almost white oval-shaped coated tablets for oral administration. The cabotegravir LA is formulated as a sterile white to slightly coloured suspension containing 400mg/2mL of cabotegravir LA for administration by IM injection.; Other Names: GSK1265744
Placebo Comparator: Placebo; Women randomised to the placebo arm will receive daily oral tablets (30 mg tablets) for approximately 30 days and thereafter will receive intra-muscular gluteal injections of Intralipid® 20% every 12 weeks	Drug: Placebo; Placebo tablets for cabotegravir are formulated as white to almost white oval-shaped coated tablets to visually match the active cabotegravir tablets. Placebo for cabotegravir injectable suspension is Intralipid® 20%. Intralipid® is a fat emulsion with no pharmacological action. It is a white, milky emulsion, consisting of purified soyabean oil, purified egg phospholipids and anhydrous glycerol. Intralipid® 20% is supplied in infusion bags.; Other Names: Intralipid® 20%

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of participants with adverse events	The incidence of increase in graded AEs and in particular liver enzymes (AST/ALT) at the level of Grade 3 or higher.	36 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Acceptability of study injections and oral tablets	Participant's opinions on the injections and tablets will be obtained through structured interviews.	24 months
Incidence of sexually transmitted infections	Incidence of HIV, HSV-2, HPV, gonorrhoea, chlamydia and trichomonas infections in women	36 months
Area under the plasma concentration versus time curve (AUC) of cabotegravir	Cabotegravir concentrations will be measured throughout the study	36 months
Impact on pregnancy	The incidence of pregnancy and pregnancy outcomes in women assigned to cabotegravir and placebo will be compared	36 months
Resistance to antiretroviral drugs	Viruses from HIV seroconverters will be sequenced and assessed for resistance mutations	36 months
HIV viral load in women who acquire HIV	HIV viral load (copies/ml) will be measured and compared between the cabotegravir and placebo arms	36 months

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Pharmacogenomics of cabotegravir	The impact of genetic polymorphisms on response to cabotagravir LA will be assessed	36 months
Impact of contraception on area under the plasma concentration versus time curve (AUC) of cabotegravir	Cabotegravir concentrations in women on DMPA will be compared to women on other forms of contraception	36 months

Collaborators and Investigators

• Sponsor: Centre for the AIDS Programme of Research in South Africa
• Collaborators: ViiV Healthcare
• Investigators: Principal Investigator: Salim S Abdool Karim, MBCHB, PhD, Centre for the AIDS Programme of Research in South Africa; Principal Investigator: Quarraisha Abdool Karim, PhD, Centre for the AIDS Programme of Research in South Africa; Principal Investigator: Leila E Mansoor, PhD, Centre for the AIDS Programme of Research in South Africa

Publications and helpful links

General Publications

• Radzio J, Spreen W, Yueh YL, Mitchell J, Jenkins L, Garcia-Lerma JG, Heneine W. The long-acting integrase inhibitor GSK744 protects macaques from repeated intravaginal SHIV challenge. Sci Transl Med. 2015 Jan 14;7(270):270ra5. doi: 10.1126/scitranslmed.3010297.
• Spreen WR, Margolis DA, Pottage JC Jr. Long-acting injectable antiretrovirals for HIV treatment and prevention. Curr Opin HIV AIDS. 2013 Nov;8(6):565-71. doi: 10.1097/COH.0000000000000002.

Study record dates

Study Major Dates

• Study Start: October 1, 2015
• Primary Completion (Anticipated): September 1, 2018
• Study Completion (Anticipated): September 1, 2018

Study Registration Dates

• First Submitted: May 27, 2015
• First Submitted That Met QC Criteria: June 3, 2015
• First Posted (Estimate): June 4, 2015

Study Record Updates

• Last Update Posted (Estimate): November 5, 2015
• Last Update Submitted That Met QC Criteria: November 4, 2015
• Last Verified: November 1, 2015

More Information

Terms related to this study

• Keywords: safety; HIV prevention; long-acting injectable; Cabotegravir; acceptability
• Additional Relevant MeSH Terms: RNA Virus Infections; Virus Diseases; Infections; Blood-Borne Infections; Communicable Diseases; Sexually Transmitted Diseases, Viral; Sexually Transmitted Diseases; Lentivirus Infections; Retroviridae Infections; Immunologic Deficiency Syndromes; Immune System Diseases; Slow Virus Diseases; HIV Infections; Acquired Immunodeficiency Syndrome; Molecular Mechanisms of Pharmacological Action; Anti-Infective Agents; Antiviral Agents; Enzyme Inhibitors; Anti-HIV Agents; Anti-Retroviral Agents; HIV Integrase Inhibitors; Integrase Inhibitors; Pharmaceutical Solutions; Parenteral Nutrition Solutions; Fat Emulsions, Intravenous; Soybean oil, phospholipid emulsion; Cabotegravir
• Other Study ID Numbers: CAPRISA 014