Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

DOR/ISL clinical trials

Also listed in trial records as MK-8591A, Doravirine/islatravir
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 5 trials in our UK, USA, Japan, Australia, Switzerland, Canada, Israel, Germany, France, Spain, Netherlands, Turkey, Mexico, Taiwan, Italy and Poland registers that name DOR/ISL as an intervention. Synced 10 Nov 2026
5Current trials
0Recruiting now
1Lead sponsor
16Country registers
At a glance

DOR/ISL is named as an intervention in 5 current clinical trials in our UK, USA, Japan, Australia, Switzerland, Canada, Israel, Germany, France, Spain, Netherlands, Turkey, Mexico, Taiwan, Italy and Poland registers. None are recruiting at the moment. All registered phases are Phase 3. The lead sponsor is Merck Sharp & Dohme LLC. The most-studied condition is HIV-1 Infection.

Patient leaflets for DOR/ISL

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Trials by status

  • Active, closed5100%

Trials by phase

  • Phase 35100%
01

Clinical trials of DOR/ISL

5 trials
StudyPhaseStatusLead sponsorRegisters
Open-label, Follow-up of Doravirine/Islatravir (DOR/ISL 100 mg/0.75mg) for Participants With Human Immunodeficiency Virus-1 (HIV-1) Infection (MK-8591A-033)
NCT04776252 · HIV-1 Infection
Phase 3 Active, closed Merck Sharp & Dohme LLC UK, USA, Germany, France, Spain, Italy, Poland, Switzerland, Canada, Japan, Australia
A Switch to Doravirine/Islatravir (DOR/ISL) in Participants With Human Immunodeficiency Virus Type 1 (HIV-1) Who Are Virologically Suppressed on Bictegravir/Emtricitabine/Tenofovir Alafenamide (BIC/FTC/TAF) (MK-8591A-052)
NCT05630755 · HIV-1 Infection
Phase 3 Active, closed Merck Sharp & Dohme LLC UK, USA, Japan, Australia, Israel
A Switch to Doravirine/Islatravir (DOR/ISL) in Participants With Human Immunodeficiency Virus Type 1 (HIV-1) Who Are Virologically Suppressed on Antiretroviral Therapy (ART) (MK-8591A-051)
NCT05631093 · HIV-1 Infection
Phase 3 Active, closed Merck Sharp & Dohme LLC UK, USA, Switzerland, Canada, Japan, Australia
DOR/ISL in HIV-1 Antiretroviral Treatment-naïve Participants (MK-8591A-053)
NCT05705349 · HIV-1 Infection
Phase 3 Active, closed Merck Sharp & Dohme LLC UK, USA, Germany, France, Spain, Netherlands, Switzerland, Turkey, Canada, Mexico, Japan, Australia, Israel
A Study of Doravirine/Islatravir (DOR/ISL, MK-8591A) for the Treatment of Human Immunodeficiency Virus 1 (HIV-1) Infection in Participants Who Previously Received DOR/ISL (MK-8591A-054)
NCT05766501 · HIV Infection
Phase 3 Active, closed Merck Sharp & Dohme LLC UK, USA, Switzerland, Canada, Japan, Taiwan, Australia, Israel

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

Conditions studied with DOR/ISL

2 conditions
HIV-1 Infection4HIV Infection1
05

Related compounds

06

Questions about DOR/ISL trials

How many clinical trials are testing DOR/ISL?

5 current trials in our UK, USA, Japan, Australia, Switzerland, Canada, Israel, Germany, France, Spain, Netherlands, Turkey, Mexico, Taiwan, Italy and Poland registers name DOR/ISL (also registered as MK-8591A) as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are DOR/ISL trials recruiting patients?

Not at the moment. None of the 5 trials in our registers is recruiting; they are active but closed to enrolment, not yet open, or enrolling by invitation. Only the study team can confirm whether a patient is eligible.

Who sponsors DOR/ISL clinical trials?

The lead sponsor is Merck Sharp & Dohme LLC. The number in brackets is how many trials each organisation leads.

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 DOR/ISL works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how DOR/ISL 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 DOR/ISL (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 10 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

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 — 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 — we correct promptly and log it.