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HivPhase 3LATANCT05154747

Long-Acting Treatment in Adolescents (LATA)

A Phase 3 study testing Cabotegravir, Rilpivirine Drug Combination and TLD in people with Hiv and HIV Infections, run by University College, London at 5 sites in 4 countries.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The LATA trial will find out if taking a long-acting injectable form of HIV medicines, called cabotegravir and rilpivirine, every 2 month works as well as taking tablet HIV medicines every day in young people aged 12-19 years of age. Read more about this study

Who is it for?
Ages 12 to 19 years
Conditions the study is for
Hiv, HIV Infections, HIV-1-infection
What is being tested?
Cabotegravir, Rilpivirine Drug Combination and TLD
Could I receive a placebo?
No, everyone receives an active treatment
How many people
476 participants
Where
5 sitesin 4 countries
Study dates
22 Jun 2023to Mar 2026
Phase
Phase 3
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 12 to 19 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Who may be able to join

  • HIV-1-infected
  • Aged 12-19 years
  • Aware of HIV status
  • Body weight ≥35Kg
  • On ART consisting of 2NRTI and a third agent
  • On ART for ≥1 year with no previous regimen change for treatment failure*
Show all 13Show fewer
  • Virologically suppressed with all HIV-1 RNA viral loads <50copies/mL¥ in the last 12 months up to and including screening. Additionally, there must be one result <50copies/mL at least 12 months prior to screening and the viral load at trial screening must be <50 copies/mL
  • Written informed consent provided by participant (if aged 18 to 19 years) and/or carer/legal guardian (if participant aged 12 to 17 years) as appropriate
  • Written informed assent in participants aged 12 to 17 years
  • Females who are sexually active must be willing to adhere to highly effective methods of contraception⌂
  • Treatment failure includes virological, immunological or clinical failure where regimen has been changed for lack of response to treatment
  • The screening sample VL must be <50 copies/mL. For samples prior to screening, a diluted sample may be used; if the viral load in the diluted sample is below lower limit of quantification (LLQ), a calculated VL<100 copies/mL is allowed; if the viral load in the diluted sample is equal or above LLQ the calculated VL should be below 50 copies/mL.
  • Highly effective contraception are injectable, implantable, oral and intrauterine contraceptives which have an expected failure rate <1% per year; in the LA group, must avoid pregnancy for 12 months after the last dose of the CAB and RPV LA

Who cannot join

  • Known HIV-2 infection
  • Females who are pregnant or breastfeeding
  • Females who plan to become pregnant during the trial follow-up or are sexually active and are unwilling to avoid pregnancy for the duration of the trial
  • Moderate or high-risk score on the Columbia-Suicide Severity Rating Scale
  • Hepatitis B SAg positive
  • ALT ≥3 x upper limit of normal
Show all 15Show fewer
  • On treatment for active TB
  • Known contraindication to receipt of dolutegravir, cabotegravir, rilpivirine, emtricitabine/ lamivudine and any formulation of tenofovir
  • Participants determined by the investigator to have a high risk of seizure, including those with unstable or poorly controlled seizure disorder
  • Unwilling or contraindication to receiving injections
  • Contraindication to receiving injectable agents in the buttock area
  • Underlying medical condition (e.g. bleeding disorder; use of warfarin) that in the opinion of the investigator precludes participation
  • Previous randomisation in the BREATHER Plus trial
  • Known major^ resistance to non-nucleoside reverse transcriptase inhibitors or integrase inhibitors
  • Major NNRTI and INSTI mutations are those listed in the IAS report (www.iasusa.org/resources/hiv-drug-resistance-mutations/ - which is likely to change over time

Trial locations and contacts

5 sites in 4 countries.

5 sites in 4 countries

Uganda2 sites
  • Baylor College of Medicine Childrens Foundation Uganda

    Kampala

  • Joint Clinical Research Centre

    Kampala

Other trials in Uganda

Kenya1 site
  • Moi University

    Eldoret

Other trials in Kenya

South Africa1 site
  • Enhancing Care Foundation King Edward VIII Hospital

    Durban

Other trials in South Africa

Zimbabwe1 site
  • University of Zimbabwe Clinical Research Centre

    Harare

Other trials in Zimbabwe

About this study

Official title: Long-Acting Treatment in Adolescents (LATA): A Randomised Open-label 2-arm 96 Week Trial in Virologically Suppressed HIV-1-positive Adolescents Aged 12-19 Years of Age in Sub-Saharan Africa

The LATA trial will find out if taking a long-acting injectable form of HIV medicines, called cabotegravir and rilpivirine, every 2 month works as well as taking tablet HIV medicines every day in young people aged 12-19 years of age.

The trial is organised by an international group of researchers from Europe and Africa, and will include 460 young people, from Kenya, South Africa, Uganda and Zimbabwe.

Read the detailed description

The goal of HIV treatment is to make sure the HIV virus in the blood remains very low; this is called having an undetectable viral load (virological suppression). If this goal is achieved and sustained life-long, then people with HIV infection can live a healthy life, with a normal life expectancy. However, it is challenging to take medication every single day for life. This may be an even bigger challenge for teenagers living with HIV.

There is now a new way of taking HIV treatment. This is through an injection form of the HIV medicines. Two injections, one of cabotegravir and one of rilpivirine, have to be given in the clinic every 8 weeks. One injection will be given in the left cheek of the buttock and the other in the right cheek of the buttock at the same visit. This is called an intramuscular (IM) injection.

In LATA, two different ways of taking HIV medicines will be compared. Participants will be randomised, with an equal chance that they will either go into the long-acting injectable group or get a daily tablet by mouth. This is what happens depending on which group they are randomised to:

  • Long-Acting Injectable Group: In this group, there are 2 options. The first is to stay on current HIV medicines by mouth and then to start the injections around 4 weeks after randomisation. If this is the choice, then at week 4, the first 2 injections will be given, the second two will be given 4 weeks later, and then it's every 8 weeks from then on. The second option is to switch to taking one tablet of cabotegravir and one tablet of rilpivirine for approximately 4-5 weeks before starting the injections. The reason that some people might choose to have the tablet forms first, is to make sure they tolerate them. This is called an oral lead-in (OLI). For the OLI group, and as long as liver test results at 4 weeks are within normal levels, the first two injections will be given at around 5 weeks (about a week after the week 4 visit), the second two are given 4 weeks later, and then it's every 8 weeks from then on.
  • Continuous Oral Treatment Group: this group will continue to take HIV medicines every day by mouth. However, to join the trial, some participants will have to change some of their oral medications as the combination being used is dolutegravir with tenofovir plus either lamivudine or emtricitabine as a single tablet taken once a day, called TLD.

The LATA trial will enrol 460 young people living with HIV-1 from Kenya, South Africa, Uganda and Zimbabwe. People taking part need to be 12 to 19 years old, HIV-1-positive, have undetectable HIV-1 viral load (HIV-1 RNA < 50 c/mL) for at least the last year, on combination ART, and never have switched HIV medication in the past because of treatment failure. In order to join, adolescents who are at least 18 years old will need to sign the consent form for themselves. The consent form describes what the trial is about and what is required of participants. Adolescents aged 12 to 17 years of age will have to sign an assent form - this assent form describes what the trial is about and what is required of participants. The assent form can be signed without a parent or guardian in the same room. The assent form has the same information in it as the consent form that their parent or guardian will also need to sign as well, to agree to them taking part in LATA. Each person taking part will stay in the trial for at least 96 weeks (about 2 years) although it may be longer, between 3-4 years. Young women enrolled in LATA must not be pregnant or breastfeeding when they join and must avoid getting pregnant during their time in the trial. For young women in the long-acting injectables group, they must also avoid getting pregnant for at least 12 months after the last injection is given; this is because not much is known about the safety of these injections in pregnancy. If, however, a young woman does get pregnant while they are on the long-acting injectables, they should immediately contact their clinic for advice and support. More details will be provided in a separate information sheet and consent form about options for HIV treatment during pregnancy, including staying on the long-acting injectables with additional monitoring.

At the beginning of the trial everyone will be screened to make sure they meet the criteria to participate, then they will be randomised - by a computer- to one of the groups in the study. For the long-acting injectable group, there are the 2 options as described above and one or two additional visits around 4-5 weeks after being randomised into the trial. People taking part in the trial will be asked to visit the clinic every 8 weeks until the last participant who joined the trial has been in the trial for 96 weeks. The trial research team will ask questions about health, wellbeing and mood at some of the visits. For girls who have started their periods, a pregnancy test will be done at each visit. Everyone will have their viral load measured approximately every 6 months and they and their doctors will receive the results, which show how much HIV virus is in the blood. At some visits a blood sample will be stored, which may be looked at later for HIV viral load or for changes to the virus that may stop some treatment working as well. An additional blood sample will also be taken at the beginning and then once a year, and urine samples at the beginning and at week 96; these stored samples will be used to look at the health of people's kidneys, bone, heart and other organ systems; they are optional. In addition, to the main trial, there are sub-studies (smaller studies within the main trial), which people taking part may be invited to take part in. Some participants in LATA will be invited to take part in a social science sub-study where there are interviews to find out how people feel about HIV and their medication. In another sub-study, the mood (neuropsychiatric) sub-study, there are additional surveys to find out if young people are having problems with feeling down or worried about HIV, their medication and other things going on in their lives. A small number of participants may be asked to take part in a study that measures the amount of HIV medicine in the blood. These sub-studies require additional consent, so people can decide if they do or don't want to take part in these sub-studies, and it won't affect being in the LATA trial. At selected sites, a further sub-study is about checking the amount of muscle and fat in the body, using a monitor placed on the arm, which doesn't hurt at all. The information for this sub-study is in the main LATA information sheet.

The trial will be able to show whether the injection forms of HIV medicine work as well as taking the daily tablets of HIV medicines in adolescents living with HIV. If the long-acting injectables given every 8 weeks work as well as the daily oral tablet, it is hoped the HIV guidelines will change to recommend this as an option for how adolescents and young people take their HIV medicines.

Being tested
Cabotegravir, Rilpivirine Drug Combination, TLD
Medical subject headings
Acquired Immunodeficiency Syndrome, HIV Infections

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Cabotegravir, Rilpivirine Drug CombinationDrug

    Also called CAB, RPV

    Cabotegravir LA 600mg as a 3mL IM injection. The product is packaged in a 3mL USP Type I glass vial. Each vial is for single-dose use. CAB LA injectable suspension is to be stored according to the product label at room temperature (<30oC). CAB LA is composed of cabotegravir free acid, polysorbate 20, polyethylene glycol3350, mannitol, and water for injection.

    Rilpivirine LA 900mg as a 3mL IM injection. Each single-dose vial contains 900mg/3mL rilpivirine. RPV LA injectable suspension should be stored according to the product label refrigerated at 2-8oC and should be protected from light. RPV LA is composed of RPV free base, poloxamer 338, sodium dihydrogen phosphate monohydrate, citric acid monohydrate, glucose monohydrate, sodium hydroxide, and water for injection.

    Cabotegravir Long-Acting (CAB LA) will be given IM into one buttock, and Rilpivirine Long-Acting (RPV LA) will be given IM into the opposite buttock.

  • TLDDrug

    Dolutegravir 50mg oral with tenofovir disoproxil fumarate (245mg) and lamivudine (300mg) in a fixed dose combination or Dolutegravir 50mg oral with tenofovir alafenamide fumarate (25mg) and lamivudine (300mg) (l/TAF) oral in a fixed dose combination

Study groups in NCT05154747
Study groupRoleWhat they receive
Continuous Therapy (CT) Control GroupActive comparatorThe control group is a continuous daily oral combination ART consisting of dolutegravir (DTG), with a tenofovir (TFV) and lamivudine(3TC)/emtricitabine(FTC) backbone
Receives: Drug: TLD
Long Acting (LA) Injectable GroupExperimentalThe intervention group is a long-acting injectable, cabotegravir (CAB) LA and rilpivirine (RPV) LA given every 8-weeks after an optional 4-week oral lead-in period with oral cabotegravir and rilpivirine, and two loading doses separated by 4 weeks.
Receives: Drug: Cabotegravir, Rilpivirine Drug Combination

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Confirmed virological rebound

    The proportion of participants with confirmed virological rebound, defined as 2 consecutive plasma HIV-RNA ≥50 copies/mL at any time up to the 96 week assessment

    Measured: Up to 96 week assessment

Secondary outcomes (20)
  1. Efficacy Outcome: Proportions of participants with HIV-RNA ≥50 copies/mL

    Proportions of participants with HIV-RNA ≥50 copies/mL at 48 and 96 weeks using a modified FDA snapshot algorithm

    Measured: At week 48 and week 96 visits

  2. Efficacy Outcome: The proportion of participants with confirmed HIV-RNA ≥1000 copies/mL

    The proportion of participants with HIV-RNA ≥1000 copies/mL (confirmed) by week 96

    Measured: Up to week 96 assessment

  3. Efficacy Outcome: The proportion of participants with confirmed HIV-RNA ≥200 copies/mL

    The proportion of participants with HIV-RNA ≥200 copies/mL (confirmed) by week 96

    Measured: Up to week 96 assessment

  4. Efficacy Outcome: The number of HIV reverse transcriptase mutations

    The number of HIV reverse transcriptase mutations in participants with confirmed virological rebound

    Measured: Up to week 96 assessment

  5. Efficacy Outcome: The number of HIV integrase mutations

    The number of HIV integrase mutations in participants with confirmed virological rebound

    Measured: Up to week 96 assessment

  6. Efficacy Outcome: HIV-RNA <50 copies/mL

    HIV-RNA <50 copies/mL at 24, 48 and 96 weeks

    Measured: At 24, 48 and 96 week assessments

  7. Safety Outcome: Change in lipids

    Changes in lipids from baseline to 96 weeks

    Measured: From baseline 96 weeks

  8. Safety Outcome: Change in HbA1c

    Changes in HbA1c from baseline to 96 weeks

    Measured: From baseline to 96 weeks

  9. Safety Outcome: Change in Phosphate

    Changes in phosphate from baseline to 96 weeks

    Measured: From baseline to 96 weeks

  10. Safety Outcome: Change in liver function: measurement of alanine aminotransferase (ALT)

    Changes in ALT from baseline to 96 weeks

    Measured: From baseline to 96 weeks

  11. Safety Outcome: Change in renal function: measurement of eGFR

    Changes in eGFR from baseline to 96 weeks

    Measured: From baseline to 96 weeks

  12. Safety Outcome: Weight changes

    Changes in weight from baseline to 48 and 96 weeks

    Measured: From baseline to 48 and 96 weeks

  13. Safety Outcome: Height changes

    Changes in height from baseline to 48 and 96 weeks

    Measured: From baseline to 48 and 96 weeks

  14. Safety Outcome: Change in resting pulse

    Changes in resting pulse from baseline to 48 and 96 weeks

    Measured: From baseline to 48 and 96 weeks

  15. Safety Outcome: Change in blood pressure

    Changes in blood pressure from baseline to 48 and 96 weeks

    Measured: From baseline to 48 and 96 weeks

  16. Safety Outcome: Time to new or recurrent WHO grade 3 or WHO grade 4 event or death

    Time to any new or recurrent WHO grade 3 or WHO grade 4 event or death

    Measured: From baseline to 96 weeks

  17. Safety Outcome: Incidence of serious, grade 3, 4 and 5, and any treatment-modifying adverse events

    Incidence of serious, grade 3, 4 and 5, and treatment-modifying (of any grade) adverse events

    Measured: From baseline to 96 weeks

  18. Safety Outcome: The proportion of participants with any change from baseline ART regimen

    The proportion of participants with any change from baseline ART regimen

    Measured: From baseline to 96 weeks

  19. Safety Outcome: Change in CD4+ and CD8+ T-cell count

    Change in CD4+ and CD8+ T-cell count from baseline to 48 and 96 weeks

    Measured: From baseline to 48 and 96 weeks

  20. Safety Outcome: incidence of injection-site reactions of any grade

    LA group only: incidence of injection-site reactions of any grade

    Measured: From baseline to 96 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Dec 2021
  2. Study start22 Jun 2023
  3. Primary completionMar 2025 (estimated)
  4. Study completionMar 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
476 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05154747
Sponsor's protocol ID
129628
Acronym
LATA
Status last verified
Apr 2024
First submitted
12 Nov 2021
Last updated
29 Apr 2024
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Data collected in the study will be available for additional research with justified scientific objectives. LATA will follow a controlled access approach to making data available outside of the trial whereby researchers make formal applications for data sharing. Where a proposal has been approved, the required Individual Participant Data (IPD) will be shared with the researchers on the Data Sharing Agreement to meet the requirements of the proposal. Proposals should be sent to mrcctu.lata@ucl.ac.uk. Further information on criteria and application can be found on the MRC CTU webpage on data sharing at the following link https://www.mrcctu.ucl.ac.uk/our-research/other-research-policy/data-sharing/.

Publications

  • Bwakura-Dangarembizi M, Chappell E, Kityo C, Anena DL, Kiilu C, Archary M, Jafta L, Mujuru HA, Nakabuye S, Akabwai GP, Siika A, Mngqibisa R, Mugerwa H, Walker S, Seeley J, Burger D, Omar A, South A, Nguyen H, Giaquinto C, Spittle B, Bamford A, Kekitiinwa AR, Ford D, Pett S; LATA trial team. Switch to injectable cabotegravir-rilpivirine given every 8 weeks in adolescents living with HIV with virological suppression in sub-Saharan Africa (LATA): a randomised, open-label, multicentre, 96-week non-inferiority trial. Lancet. 2026 Sep 17:S0140-6736(26)01537-0. doi: 10.1016/S0140-6736(26)01537-0. Online ahead of print.

    PubMed 42753775
  • Anena D, Chappell E, Nazzinda R, Kiilu C, Chitsamatanga M, Arumugam T, Green A, Kityo Mutuluuza C, Bwakura-Dangarembizi M, Siika A, Archary M, Jafta L, Namukwaya S, Seeley J, Akabwai G, Mugerwa H, Bevers L, Burger D, Walker S, Bamford A, South A, Apoto N, Bush M, Thomason MJ, Spittle B, Ford D, Kekitiinwa AR, Pett SL; LATA Trial Team. Trial design and enrolment characteristics of LATA (Long-Acting Treatment in Adolescents): A randomised, open-label, non-inferiority, 96-week trial evaluating the virological efficacy, safety, acceptability and quality-of-life of the dual long-acting injectable regimen cabotegravir/ rilpivirine compared to daily oral therapy in virologically suppressed adolescents with HIV-1 infection, aged 12 to <20 years, in Sub-Saharan Africa. Contemp Clin Trials. 2026 Mar;162:108213. doi: 10.1016/j.cct.2025.108213. Epub 2026 Jan 7.

    PubMed 41512916

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Cabotegravir, Rilpivirine Drug Combination and TLD in people with Hiv and HIV Infections, run by University College, London at 5 sites in 4 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 13 inclusion and 15 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 29 Apr 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 5 sites in Uganda, Kenya, South Africa, Zimbabwe. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Confirmed virological rebound (time frame: Up to 96 week assessment). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05154747, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Apr 2024.

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