๐Ÿ‡ฎ๐Ÿ‡ชIreland
16ยฐC Partly Cloudy ยท Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Priya Life Science Compound trial record
Trackers Drugs Trial finder
Compound · clinical trials

Cabotegravir clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 7 trials in our USA and UK registers that name Cabotegravir as an intervention. Synced 26 Sep 2026
7Current trials
3Recruiting now
2Lead sponsors
2Country registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards
At a glance

Cabotegravir is named as an intervention in 7 current clinical trials in our USA and UK registers. 3 are recruiting patients now. The most common phase is Phase 3. The sponsor with the most trials is ViiV Healthcare (5). The most-studied condition is HIV Infections. The EU clinical trials register (CTIS) separately lists 1 authorised or ongoing trial.

Trials by status

  • Recruiting343%
  • Active, closed457%

Trials by phase

  • Phase 3457%
  • Phase 2114%
  • Observational114%
  • Phase 1114%
01

Clinical trials of Cabotegravir

7 trials
StudyPhaseStatusLead sponsorRegisters
Study of Lenacapavir, Teropavimab, and Zinlirvimab Versus Cabotegravir and Rilpivirine in Virologically Suppressed Adults With HIV-1 on Oral Daily Antiretroviral Therapy
NCT07682961 · HIV Infections
Phase 3 Recruiting Gilead Sciences USA
A Study to Investigate Pharmacokinetics, Safety and Tolerability of Long-Acting Cabotegravir Plus Recombinant Human Hyaluronidase PH20 in Healthy Adult Participants
NCT05418868 · ClinicalTrials.gov ↗ · HIV Infections
Phase 1 Recruiting ViiV Healthcare USA
Implementation Study of Lenacapavir Pre-exposure Prophylaxis for HIV Prevention
NCT07473778 · ClinicalTrials.gov ↗ · HIV Infections
Observational Recruiting Gilead Sciences USA
Study to Evaluate the Efficacy, Safety, and Tolerability of Long-acting Intramuscular Cabotegravir and Rilpivirine for Maintenance of Virologic Suppression Following Switch From an Integrase Inhibitor in HIV-1 Infected Therapy Naive Participants
NCT02938520 · HIV Infections
Phase 3 Active, closed ViiV Healthcare UK, USA
Study Evaluating the Efficacy, Safety, and Tolerability of Switching to Long-acting Cabotegravir Plus Long-acting Rilpivirine From Current Antiretroviral Regimen in Virologically Suppressed HIV-1-infected Adults
NCT02951052 · ClinicalTrials.gov ↗ · Infection, Human Immunodeficiency Virus, HIV Infections
Phase 3 Active, closed ViiV Healthcare USA
Efficacy, Safety and Tolerability Study of Long-acting Cabotegravir Plus Long-acting Rilpivirine (CAB LA + RPV LA) in Human-immunodeficiency Virus-1 (HIV-1) Infected Adults
NCT03299049 · ClinicalTrials.gov ↗ · HIV Infections
Phase 3 Active, closed ViiV Healthcare USA
A Study to Investigate the Virologic Efficacy and Safety of VH3810109 + Cabotegravir Compared to Standard of Care (SOC) in Male and Female Adults Living With Human Immunodeficiency Virus (HIV)
NCT05996471 · HIV Infections
Phase 2 Active, closed ViiV Healthcare USA

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Cabotegravir in the EU trials register (CTIS)

1 trial

Authorised or ongoing trials in the EU Clinical Trials Information System that list a product containing Cabotegravir. Many trials are registered in both CTIS and ClinicalTrials.gov, so these are shown separately rather than added to the count above. Trials with a site in Ireland are listed first.

StudyPhaseStatusSponsorCountries
A Phase 3, Randomized, Open-label Study to Evaluate the Efficacy and Safety of Switching to Long-acting Antiretroviral Therapy of Broadly Neutralizing Antibodies Teropavimab and Zinlirvimab in Combination With the Capsid Inhibitor Lenacapavir Twice-Yearly Versus Cabotegravir and Rilpivirine Every 8 Weeks in Virologically Suppressed Adults With HIV-1 on Oral Daily Antiretroviral Therapy
2025-524335-39-00 · Virus Diseases
Phase 3 Ongoing Gilead Sciences Inc Netherlands, Poland, Germany + 3 more
03

Cabotegravir across our data

Ireland · EU · US

The same active substance in our other registers, matched by its exact name. Each entry links to the register record it comes from.

Licensed in Ireland (HPRA)

3 single-substance products containing Cabotegravir on the HPRA medicines list.

  • Vocabria 30 mg film-coated tabletsViiV Healthcare BV · EU/1/20/1481/001
  • Vocabria 400 mg prolonged-release suspension for injectionViiV Healthcare BV · EU/1/20/1481/002
  • Vocabria 600 mg prolonged-release suspension for injectionViiV Healthcare BV · EU/1/20/1481/003
All 3 Irish products →

Supply shortages

No entry for Cabotegravir in the EMA, FDA or German BfArM shortage lists we track.

04

Conditions studied with Cabotegravir

2 conditions
HIV Infections7Infection, Human Immunodeficiency Virus1
05

Sponsors

lead sponsor per trial
Lead sponsorTrials
ViiV Healthcare5
Gilead Sciences2
06

By country register

RegisterTrialsRecruiting
Clinical trials in USA73
Clinical trials in UK10
EU register (CTIS)1—

A trial with sites in more than one country appears in each of those registers. CTIS does not publish a recruiting flag; its trials may also appear in the registers above.

07

Related compounds

08

Questions about Cabotegravir trials

How many clinical trials are testing Cabotegravir?

7 current trials in our USA and UK registers name Cabotegravir as a drug or biological intervention, as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are Cabotegravir trials recruiting patients?

Yes. 3 of the 7 trials are recruiting: 3 with sites in USA. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Cabotegravir clinical trials?

ViiV Healthcare (5) and Gilead Sciences (2). The number in brackets is how many trials each organisation leads.

Is Cabotegravir licensed in Ireland?

Yes. The HPRA medicines list includes 3 single-substance products containing Cabotegravir, for example Vocabria 30 mg film-coated tablets (ViiV Healthcare BV). A licence does not mean a product is currently marketed or reimbursed; see each product's record.

Is there a Cabotegravir shortage?

Not in the lists we track: Cabotegravir has no entry in the EMA, FDA or German BfArM shortage registers as of their latest sync.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Cabotegravir works or whether it is effective, and it is not medical advice.

Approvals, shortages and trials, every Friday

One email a week with new EMA and FDA approvals, EU and US medicine shortages, how many trials are recruiting in Ireland, and the week's Irish pharma news.

Free. Unsubscribe from any email with one click. See our privacy policy.

How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records โ€” it is not written from memory, and nothing here describes how Cabotegravir works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Cabotegravir (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 26 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician โ€” our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us โ€” we correct promptly and log it.