• 06 May 2024
• Admin
• News Article

MHRA Grants Marketing Approval For ViiV Healthcare’s Cabotegravir Formulations

UK MHRA grants marketing approval for ViiV Healthcare’s cabotegravir formulations to help prevent HIV-1 infection in adults and adolescents

Overview

The UK Medicines and Healthcare products Regulatory Agency (MHRA) has on 3rd May, 2024 approved two new formulations of the medicine cabotegravir (Apretude 30 mg film-coated tablets and Apretude 600 mg prolonged-release suspension for injection) to help prevent sexually transmitted HIV-1 infection (pre-exposure prophylaxis or PrEP) in adults and adolescents weighing at least 35kg who are at an increased risk of infection. Cabotegravir has been authorised as tablets and as a long-acting injection administered every two months.

New marketing authorization: - The new marketing authorisation was granted on 3rd May, 2024 to ViiV Healthcare UK Limited.

Tablet-based PrEP

• Tablet-based PrEP is already available for those at risk. 
• Cabotegravir would provide an alternative HIV prevention treatment option for eligible individuals should it be recommended by NICE. 
• Cabotegravir 600 mg long-acting injection is the first injectable treatment approved to help prevent HIV-1 infection in the UK.

HIV

• HIV (human immunodeficiency virus) is a virus that damages the cells in the immune system and weakens its ability to fight everyday infections and diseases. 
• There are two primary strains, HIV-1 and HIV-2, with HIV-1 being more common. 
• When a person contracts HIV-1, the virus begins to infect a specific type of immune cell called CD4, essential for the body’s immune response.

Both formulations of cabotegravir (tablets and long-acting injection) have been authorised by the MHRA for Great Britain under a national application procedure.

Words from MHRA

• Julian Beach, MHRA Interim executive director, healthcare quality and access, said: Keeping patients safe and enabling their access to high quality, safe and effective medical products are key priorities for us.
• We’re assured that the appropriate regulatory standards for the approval of this medicine have been met.
• As with all products, we will keep its safety under close review.

Cabotegravir Dosage Forms

• Patients must have a HIV-negative test before taking cabotegravir. 
• Cabotegravir 600 mg long-acting injection is administered by a nurse or doctor into the buttock muscle six times a year. 
• Initially, patients receive one injection each month for two months, followed by one every two months. 
• Before starting the injections, patients can take cabotegravir 30 mg tablets daily for a month in consultation with their doctor to assess whether it’s appropriate to proceed with injections (oral lead-in). 
• Cabotegravir should be used in combination with safer sex practices, such as use of condoms.

Integrase Inhibitors (INIs)

• Cabotegravir belongs to a group of anti-retroviral medicines called integrase inhibitors (INIs). 
• In case of exposure to the virus, it works by blocking an enzyme called integrase that the HIV-1 virus needs to replicate itself in the body, reducing the risk of the virus multiplying and spreading from the site of infection.

Study Behind Approval

• This approval is supported by evidence from two main studies that compared cabotegravir to standard PrEP (tenofovir disoproxil fumarate/emtricitabine) for preventing HIV over a period of approximately 3 years (153 weeks). 
• In one study involving around 4,500 HIV-negative cisgender men and transgender women who have sex with men, there was a 66% reduction in HIV-1 incidence among those who received cabotegravir compared to the standard treatment. 
• In the second study, involving over 3,200 HIV-negative cisgender women, there was an 88% reduction in HIV-1 incidence among those taking cabotegravir compared to standard PrEP.

Side Effects of the Cabotegravir

• The most common side effects of the cabotegravir (which may affect more than 1 in 10 people) include headache, diarrhoea feeling hot (pyrexia) and changes in liver function (increased transaminases) as measured in blood tests. 
• Additionally, for the injection presentation, common side effects at the injection site include pain and discomfort, and the development of a hardened mass (induration) or lump (nodule).  
• Reporting system
• As with any medicine, the MHRA will keep the safety and effectiveness of cabotegravir under close review. 
• Anyone who suspects they are having a side effect from this medicine are encouraged to talk to their doctor, pharmacist or nurse and report it directly to the Yellow Card scheme, either through the website (https://yellowcard.mhra.gov.uk/) or by searching the Google Play or Apple App stores for MHRA Yellow Card.

About MHRA

• The Medicines and Healthcare products Regulatory Agency (MHRA) is responsible for regulating all medicines and medical devices in the UK by ensuring they work and are acceptably safe.
• All our work is underpinned by robust and fact-based judgements to ensure that the benefits justify any risks.