ViiV Healthcare is 100% focused on the needs of people living with and those at risk of acquiring HIV. We seek to make our medicines widely available to those in need - regardless of income or where they live, driven by public health needs - through innovative access mechanisms and partnerships, including voluntary licensing.

We are actively engaging with partners about cabotegravir LA for PrEP to find the best approach to ensure this important medicine reaches those who could benefit from it as quickly as possible.

We are proud that through our voluntary licences for dolutegravir, both directly with generic manufacturers and via the UN-backed Medicines Patent Pool, we have successfully broadened access to this WHO-recommended 1st and 2nd line treatment, with at least 21.3 million people living with HIV taking a generic dolutegravir-based regimen in low- and middle-income countries by the end of September 2021.1

We are equally committed to supporting access to cabotegravir LA for HIV Pre-Exposure Prophylaxis (PrEP), for populations with highest unmet needs. We are excited about the potential impact that cabotegravir LA for PrEP can have on the HIV epidemic, especially for women of reproductive age who are disproportionately impacted by HIV in Sub-Saharan Africa. We are clear that this must be achieved in a sustainable way, centred on partnership and integration into existing healthcare services and HIV prevention programmes.

Voluntary licenses have helped enable access for some oral ARVs through partnerships with generic manufacturers. We are committed to working with partners to find solutions which enable broader access to cabotegravir LA for PrEP with the goal of being able to enable lower prices and/or increased capacity. However, there are some very real complexities that need to be considered and addressed when introducing a very innovative medicine such as cabotegravir LA for PrEP in resource limited settings.

To better understand the considerations involved and evaluate the feasibility of voluntary licenses, ViiV Healthcare has conducted a rigorous assessment, with inputs from several generic manufacturers and contract manufacturing organisations. The assessment concluded that securing a generic partner for cabotegravir LA for PrEP will be challenging, due to the complexities of manufacturing, regulatory requirements, capital investment needs and unpredictable demand.

We are continuing to work with the Medicines Patent Pool and other partners and remain open to the potential for voluntary licenses for cabotegravir LA for PrEP in the future.

Unless and until we have a generic partner, we anticipate that we will be the sole supplier of cabotegravir LA for PrEP globally, including in resource-limited settings at least during the initial years of introduction of the medicine.

We will focus on collaborations to enable implementation science projects that will provide critical information on the feasibility, acceptability, and future adoption of cabotegravir LA for PrEP into national programmes, in line with WHO recommendations and the recent summary from the WHO-led Conference on Antiretroviral Drug Optimization (CADO).

We will continue to work with partners and consortia to ensure clinical-need driven access to cabotegravir LA for PrEP is possible outside of voluntary licenses in developing countries and that sufficient supply is available to meet these important goals.

NP-GBL-HVX-COCO-220038 - March 2022

Media contacts

For our corporate press office, email: Rachel Jaikaran

OR call +44 7823 523 755

For US-specific media enquiries, email: Audrey Abernathy

OR call +1 919 605 4521

Reporting of side effects

If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in the package leaflet. You can also report side effects directly via the Yellow Card Scheme at or search for MHRA Yellowcard in the Google Play or Apple App store. By reporting side effects, you can help provide more information on the safety of this medicine.

If you are from outside the UK, you can report adverse events to GSK/ViiV by selecting your region and market, here.