PLX8394 clinical trials
Also written Plixorafenib, FORE8394 and PLX8394.
How each study uses PLX8394 is sorted by a rule, right about nine times in ten. Readers can ask us to read every study one by one.Ask us to read each study
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Example · made-up studies
Breast cancer · Recruiting: 2 came in, 3 changed
What changed in your saved searches, Oct 31 – Nov 6:
A study of drug A after surgery for early breast cancer
Came in · now Recruiting
Drug B with hormone therapy in advanced breast cancer
Changed
· Sites: 4 added, including Seoul and Busan
· Enrollment: 300 → 450 participants
Exercise during chemotherapy
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Approvals
The first approval found in each region, with its record
- United States
- Not in FDA's approval records
- European Union
- Not in EMA's list of EU-wide authorisations
From FDA's Drugs@FDA and Purple Book (through openFDA) and the European Medicines Agency, files of Sept 2026 and 27 Oct 2026. National approvals in Europe and other countries are not included. How this is worked out
How studies write it
Studies that test it under each name
Studies by the year they started
5 studies that test it; most in 2014 (1); 1 more planned to start later
| Year | Studies |
|---|---|
| 2014 | 1 |
| 2015 | 1 |
| 2023 | 1 |
| 2024 | 1 |
| 2025 | 1 |
By phase
A phase 1/2 study counts in both.
What it is tested for
Each study’s main condition, where its own words name it, so a study counts once.
Who runs them
Industry 4 · Other 2
Fore Biotherapeutics (4) · Olivia Newton-John Cancer Research Institute (1) · Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins (1)
Often tested with
Tested in the same studies.
Related medicines
As reviewed, each with the page that says it.
- One of Protein Kinase Inhibitors source
Coming up
From the study records. Dates are the sponsors’ own estimates and often move.
Reaching primary completion within a year · 1
Studies that test PLX8394.
- Jun 2027A Trial to Evaluate CSF ctDNA and Safety of Plixorafenib Alone or With Retifanlimab in Patients With BRAF-altered GliomaEarly Phase 1 · Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Studies
Open first, then newest update. How each study uses PLX8394 is read from its arms, and is right about nine times in ten. Ask us to read each study. These are the studies that list it as an intervention; a search of ClinicalTrials.gov also finds studies that mention it only in a description, such as earlier treatment.
Testing it · 6
- Biomarker-guided RAdiation-deferring Treatment in Younger GBM Patients - Pilot StudyNot yet recruitingEarly Phase 1Olivia Newton-John Cancer Research InstituteNCT07908147Written as Plixorafenib
- A Trial to Evaluate CSF ctDNA and Safety of Plixorafenib Alone or With Retifanlimab in Patients With BRAF-altered GliomaRecruitingEarly Phase 1Sidney Kimmel Comprehensive Cancer Center at Johns HopkinsNCT06610682Written as Plixorafenib
- A Study to Assess the Efficacy and Safety of FORE8394 in Participants With Cancer Harboring BRAF AlterationsRecruitingPhase 2Fore BiotherapeuticsNCT05503797Written as Plixorafenib
- A Study of the Effects of Food and Cobicistat on Plixorafenib Pharmacokinetics in Healthy Participants.CompletedPhase 1Fore BiotherapeuticsNCT06385119Written as Plixorafenib
- A Study of FORE8394 as a Single Agent in Patients With Advanced Unresectable Solid TumorsCompletedPhase 1/2Fore BiotherapeuticsNCT02428712Written as FORE8394
- Phase I/IIa Study to Evaluate the Safety, PK, PD, and Preliminary Efficacy of PLX8394 in Patients With Advanced Cancers.TerminatedPhase 1Fore BiotherapeuticsNCT02012231Written as PLX8394
Codes
What other systems call PLX8394 · ClinicalTrials.gg INT000341
- UNII (FDA) J2L7Z273SGPLIXORAFENIBConfirmed FDA, Wikidata
- Wikidata Q27088419PLX8394Confirmed FDA, Wikidata
- DrugBank DB16038One source Wikidata
| System | Code | Name there | Checked by |
|---|---|---|---|
| UNII (FDA) | J2L7Z273SG | PLIXORAFENIB | Confirmed FDA, Wikidata |
| Wikidata | Q27088419 | PLX8394 | Confirmed FDA, Wikidata |
| DrugBank | DB16038 | — | One source Wikidata |
“Confirmed” means two independent publishers link the code to this drug; “one source”, one does and its name agrees.