Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

Plixorafenib clinical trials

Also listed in trial records as FORE8394, PLX8394, PLX-8394
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our Australia, UK, USA, Germany, France, Spain, Italy, Netherlands, Sweden, Norway, Canada and South Korea registers that name Plixorafenib as an intervention. Synced 2 Nov 2026
2Current trials
1Recruiting now
2Lead sponsors
12Country registers
At a glance

Plixorafenib is named as an intervention in 2 current clinical trials in our Australia, UK, USA, Germany, France, Spain, Italy, Netherlands, Sweden, Norway, Canada and South Korea registers. 1 is recruiting patients now. The most common phase is Phase 2. The sponsor with the most trials is Fore Biotherapeutics (1). The most-studied condition is Cancer Harboring BRAF Alterations.

Patient leaflets for Plixorafenib

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

  • Recruiting150%
  • Not yet open150%

Trials by phase

  • Phase 2150%
  • Early Phase 1150%
01

Clinical trials of Plixorafenib

2 trials
StudyPhaseStatusLead sponsorRegisters
A Study to Assess the Efficacy and Safety of FORE8394 in Participants With Cancer Harboring BRAF Alterations
NCT05503797 · Cancer Harboring BRAF Alterations, HGG, LGG
Phase 2 Recruiting Fore Biotherapeutics UK, USA, Germany, France, Spain, Italy, Netherlands, Sweden, Norway, Canada, South Korea, Australia
Biomarker-guided RAdiation-deferring Treatment in Younger GBM Patients - Pilot Study
NCT07908147 · ClinicalTrials.gov ↗ · IDH Wildtype Glioblastoma, Glioblastoma (GBM)
Early Phase 1 Not yet open Olivia Newton-John Cancer Research Institute 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 Plixorafenib

6 conditions
Cancer Harboring BRAF Alterations1HGG1LGG1Solid Tumors1IDH Wildtype Glioblastoma1Glioblastoma (GBM)1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Fore Biotherapeutics1
Olivia Newton-John Cancer Research Institute1
04

By country register

RegisterTrialsRecruiting
Clinical trials in Australia21
Clinical trials in UK11
Clinical trials in USA11
Clinical trials in Germany11
Clinical trials in France11
Clinical trials in Spain11
Clinical trials in Italy11
Clinical trials in Netherlands11
Clinical trials in Sweden11
Clinical trials in Norway11
Clinical trials in Canada11
Clinical trials in South Korea11

A trial with sites in more than one country appears in each of those registers.

05

Related compounds

06

Questions about Plixorafenib trials

How many clinical trials are testing Plixorafenib?

2 current trials in our Australia, UK, USA, Germany, France, Spain, Italy, Netherlands, Sweden, Norway, Canada and South Korea registers name Plixorafenib (also registered as FORE8394) as a drug or biological intervention, as of the registry sync on 2 November 2026. Completed and withdrawn studies are not counted.

Are Plixorafenib trials recruiting patients?

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

Who sponsors Plixorafenib clinical trials?

Fore Biotherapeutics (1) and Olivia Newton-John Cancer Research Institute (1). 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 Plixorafenib 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 Plixorafenib 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 Plixorafenib (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 2 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.