Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

Bexicaserin clinical trials

Also listed in trial records as LP352
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 3 trials in our UK, USA, China, Germany, France, Spain, Italy, Belgium, Portugal, Canada, Brazil, Mexico, Japan, Australia, Netherlands and Denmark registers that name Bexicaserin as an intervention. Synced 14 Nov 2026
3Current trials
0Recruiting now
1Lead sponsor
16Country registers
At a glance

Bexicaserin is named as an intervention in 3 current clinical trials in our UK, USA, China, Germany, France, Spain, Italy, Belgium, Portugal, Canada, Brazil, Mexico, Japan, Australia, Netherlands and Denmark registers. None are recruiting at the moment. All registered phases are Phase 3. The lead sponsor is Longboard Pharmaceuticals. The most-studied condition is Developmental and Epileptic Encephalopathy.

How Bexicaserin works

All drug targets →
Diseases it has been tested for in clinical trials, by furthest phase
  • Developmental and epileptic encephalopathyPhase 2

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL5314507, CC BY-SA 3.0. The Guide to Pharmacology has no record of this medicine, so its targets rest on ChEMBL alone. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

Patient leaflets for Bexicaserin

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, closed267%
  • By invitation133%

Trials by phase

  • Phase 33100%
01

Clinical trials of Bexicaserin

3 trials
StudyPhaseStatusLead sponsorRegisters
A Study to Investigate LP352 in Children and Adults With Developmental and Epileptic Encephalopathy (DEE)
NCT06908226 · Developmental and Epileptic Encephalopathy
Phase 3 By invitation Longboard Pharmaceuticals UK, USA, China, Germany, France, Spain, Italy, Netherlands, Belgium, Portugal, Canada, Brazil, Mexico, Japan, Australia
A Phase 3, Placebo-Controlled Study to Investigate LP352 in Children and Adults With Dravet Syndrome (DS)
NCT06660394 · Dravet Syndrome
Phase 3 Active, closed Longboard Pharmaceuticals UK, USA, China, Germany, France, Spain, Italy, Belgium, Denmark, Portugal, Canada, Brazil, Mexico, Japan, Australia
A Study to Investigate LP352 in Children and Adults With Developmental and Epileptic Encephalopathies (DEE)
NCT06719141 · Developmental and Epileptic Encephalopathy
Phase 3 Active, closed Longboard Pharmaceuticals UK, USA, China, Germany, France, Spain, Italy, Netherlands, Belgium, Portugal, Canada, Brazil, Mexico, Japan, 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 Bexicaserin

2 conditions
Developmental and Epileptic Encephalopathy2Dravet Syndrome1
05

Questions about Bexicaserin trials

How many clinical trials are testing Bexicaserin?

3 current trials in our UK, USA, China, Germany, France, Spain, Italy, Belgium, Portugal, Canada, Brazil, Mexico, Japan, Australia, Netherlands and Denmark registers name Bexicaserin (also registered as LP352) as a drug or biological intervention, as of the registry sync on 14 November 2026. Completed and withdrawn studies are not counted.

Are Bexicaserin trials recruiting patients?

Not at the moment. None of the 3 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 Bexicaserin clinical trials?

The lead sponsor is Longboard Pharmaceuticals. 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 Bexicaserin 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 Bexicaserin 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 Bexicaserin (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 14 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.