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Priya Life Science Compound trial record
Compound · clinical trials

Osavampator clinical trials

Also listed in trial records as NBI-1065845, TAK-653
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 5 trials in our USA, Canada, UK, Spain, Italy, Belgium, Poland, Taiwan, Netherlands, Sweden, Czechia, South Korea and Australia registers that name Osavampator as an intervention. Synced 28 Oct 2026
5Current trials
5Recruiting now
1Lead sponsor
13Country registers
At a glance

Osavampator is named as an intervention in 5 current clinical trials in our USA, Canada, UK, Spain, Italy, Belgium, Poland, Taiwan, Netherlands, Sweden, Czechia, South Korea and Australia registers. 5 are recruiting patients now. All registered phases are Phase 3. The lead sponsor is Neurocrine Biosciences. The most-studied condition is Major Depressive Disorder.

Patient leaflets for Osavampator

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

  • Recruiting5100%

Trials by phase

  • Phase 35100%
01

Clinical trials of Osavampator

5 trials
StudyPhaseStatusLead sponsorRegisters
Study to Assess the Efficacy and Safety of NBI-1065845 as an Adjunctive Treatment in Participants With Major Depressive Disorder (MDD)
NCT06786624 · ClinicalTrials.gov ↗ · Major Depressive Disorder
Phase 3 Recruiting Neurocrine Biosciences USA
NBI-1065845-MDD3025: Study to Assess the Efficacy and Safety of NBI-1065845 as an Adjunctive Treatment in Participants With Major Depressive Disorder (MDD)
NCT06911112 · Major Depressive Disorder
Phase 3 Recruiting Neurocrine Biosciences USA
NBI-1065845-MDD3026: Study to Assess the Efficacy and Safety of NBI-1065845 as an Adjunctive Treatment in Participants With Major Depressive Disorder (MDD)
NCT06963021 · Major Depressive Disorder
Phase 3 Recruiting Neurocrine Biosciences UK, USA, Belgium, Canada
Long-Term Study to Assess the Safety and Tolerability of NBI-1065845 as an Adjunctive Treatment in Participants With Major Depressive Disorder (MDD)
NCT06966401 · Major Depressive Disorder
Phase 3 Recruiting Neurocrine Biosciences UK, USA, Spain, Italy, Netherlands, Belgium, Sweden, Poland, Czechia, Canada, Taiwan
A Study to Evaluate the Maintenance Effect of Osavampator as an Adjunctive Treatment in Participants With Major Depressive Disorder (MDD)
NCT07196501 · Major Depressive Disorder
Phase 3 Recruiting Neurocrine Biosciences USA, Spain, Italy, Poland, Canada, South Korea, Taiwan, Australia

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 Osavampator

1 condition
05

Related compounds

06

Questions about Osavampator trials

How many clinical trials are testing Osavampator?

5 current trials in our USA, Canada, UK, Spain, Italy, Belgium, Poland, Taiwan, Netherlands, Sweden, Czechia, South Korea and Australia registers name Osavampator (also registered as NBI-1065845) as a drug or biological intervention, as of the registry sync on 28 October 2026. Completed and withdrawn studies are not counted.

Are Osavampator trials recruiting patients?

Yes. 5 of the 5 trials are recruiting: 5 with sites in USA, 3 with sites in Canada, 2 with sites in UK, 2 with sites in Spain, 2 with sites in Italy, 2 with sites in Belgium, 2 with sites in Poland, 2 with sites in Taiwan, 1 with sites in Netherlands, 1 with sites in Sweden, 1 with sites in Czechia, 1 with sites in South Korea and 1 with sites in Australia. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Osavampator clinical trials?

The lead sponsor is Neurocrine Biosciences. 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 Osavampator 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 Osavampator 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 Osavampator (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 28 Oct 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.