Vemurafenib clinical trials
Vemurafenib is named as an intervention in 14 current clinical trials in our USA, France, Italy, Canada, South Korea, Australia, China, Germany, Spain, Brazil, Israel, Poland, Czechia, Turkey, Belgium, Denmark, Mexico, Japan, UK, Netherlands, Portugal, Taiwan and Singapore registers. 7 are recruiting patients now. The most common phase is Phase 2. The sponsor with the most trials is Hoffmann-La Roche (2). The most-studied condition is Solid Tumors.
Where Vemurafenib is approved
All regulators →Of the three regulators tracked here, the first to approve Vemurafenib was the US, on 17 Aug 2011. It is approved in 3 of the 3 regulators tracked here.
- 2 EU orphan designations, most recently for treatment of Erdheim-Chester disease (27 Feb 2017, positive)
From the regulators' own registers: FDA Drugs@FDA, the EMA medicines list and Health Canada's Notice of Compliance database. Dates are the first listed approval of a product containing only this substance; combination products and nationally authorised EU medicines are not counted.
Vemurafenib patents and exclusivity
Expiry tracker →Protections still running for marketed products containing Vemurafenib, as listed by the regulators. Expired patents and exclusivities, and discontinued products, are not shown.
- 3 listed patents; the last listed expires 6 Jun 2032 (US 9447089).
- Latest patent on the drug substance itself: 27 Jul 2030 (US 8741920).
Reproduced from the FDA Orange Book and Purple Book (checked 8 Nov 2026) and the European Commission's Union Register of medicinal products (CC BY 4.0; the EU expiry date is calculated exactly as the Commission's register displays it). Listed patents and dates are as submitted to or published by the regulator and may not reflect litigation, invalidation, settlements, lapsed fees or later extensions. This is not legal advice or a freedom-to-operate opinion, and it does not say when a generic or biosimilar will launch.
What health systems spend on Vemurafenib
All medicines →From NHSBSA Prescription Cost Analysis (Open Government Licence v3.0) and CMS State Drug Utilization Data. Both are gross amounts: neither system publishes its discounts or rebates per drug. Products combining several substances are not counted here.
How Vemurafenib works
All drug targets →- Serine/threonine-protein kinase B-raf inhibitor InhibitorTarget: BRAF B-Raf proto-oncogene, serine/threonine kinase✓ In ChEMBL and the Guide to Pharmacology
- Colorectal cancerPhase 3
- Cutaneous melanomaPhase 3
- CancerPhase 2/3
- Childhood malignant neoplasmPhase 2/3
- Non-small cell lung carcinomaPhase 2/3
- B-cell chronic lymphocytic leukemiaPhase 2
- Erdheim-Chester diseasePhase 2
- HistiocytosisPhase 2
- Langerhans cell histiocytosisPhase 2
- Acute myeloid leukemiaPhase 2
Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL1229517, CC BY-SA 3.0. Targets checked against the IUPHAR/BPS Guide to PHARMACOLOGY (2026.3.1), ligand 5893, CC BY-SA 4.0. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.
NICE appraisals of Vemurafenib
All NICE appraisals →NICE, which decides whether the NHS in England should fund new medicines, has published 1 technology appraisal of Vemurafenib. 1 is current, and 1 of it recommends it for at least some patients.
| Appraisal | NICE recommendation | Published | Status |
|---|---|---|---|
| Vemurafenib for treating locally advanced or metastatic BRAF V600 mutation‑positive malignant melanoma NICE TA269 | Recommended | 12 Dec 2012 Updated 1 Jan 2015 | Current |
NICE decisions apply to the NHS in England. In Ireland the HSE decides on reimbursement, advised by the National Centre for Pharmacoeconomics. Titles, categories and dates link to the guidance on nice.org.uk. © NICE 2026 technology appraisal guidance. Available from www.nice.org.uk/guidance. All rights reserved. Subject to Notice of rights. NICE guidance is prepared for the National Health Service in England. All NICE guidance is subject to regular review and may be updated or withdrawn. NICE accepts no responsibility for the use of its content in this product/publication.
Patient leaflets for Vemurafenib
The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.
- IEIreland: 1 product on the HPRA listEach product record links to the HPRA, which publishes the leaflet and SmPC.
- EUEuropean Union: ZelborafEMA product information: package leaflet and summary of product characteristics in every EU language.
- UKUnited Kingdom: Search MHRA ProductsPatient information leaflets and SmPCs for UK-licensed products.
- USUnited States: Search DailyMedFDA-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.
Reference identifiers for Vemurafenib
- ATC code
- L01XE15
- ChEMBL
- CHEMBL1229517
- DrugBank
- DB08881
- PubChem CID
- 42611257
- CAS number
- 918504-65-1
- FDA UNII
- 207SMY3FQT
- Wikidata
- Q423111
- Wikipedia
- Vemurafenib
Codes that identify this medicine in other databases, from Wikidata (CC0), matched by its ChEMBL ID. The ATC code is the WHO classification of what the medicine is used for.
Trials by status
Trials by phase
Clinical trials of Vemurafenib
14 trialsRegisters 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.
Vemurafenib across our data
Ireland · EU · USThe same active substance in our other registers, matched by its exact name. Each entry links to the register record it comes from.
Licensed in Ireland (HPRA)
1 single-substance product containing Vemurafenib on the HPRA medicines list.
- Zelboraf 240 mg film-coated tabletsRoche Registration GmbH · EU/1/12/751/001
Supply shortages
No entry for Vemurafenib in the EMA, FDA or German BfArM shortage lists we track.
Conditions studied with Vemurafenib
24 conditionsAll 24 conditions
| Condition (as registered) | Trials |
|---|---|
| Solid Tumors | 2 |
| Cancer | 2 |
| Non-Small Cell Lung Cancer | 1 |
| Non-small Cell Lung Cancer | 1 |
| Colorectal Cancer Metastatic | 1 |
| Colorectal Carcinoma | 1 |
| Rare Tumor | 1 |
| Hematologic Cancers | 1 |
| Metastatic Cancers | 1 |
| Melanoma | 1 |
| Tumors | 1 |
| Neoplasms | 1 |
| Neoplasia | 1 |
| Histiocytosis | 1 |
| Lymphoma, Non-Hodgkin | 1 |
| Multiple Myeloma | 1 |
| Advanced Solid Tumors | 1 |
| Advanced Malignant Solid Neoplasm | 1 |
| Ann Arbor Stage III Non-Hodgkin Lymphoma | 1 |
| Ann Arbor Stage IV Non-Hodgkin Lymphoma | 1 |
| Histiocytic Sarcoma | 1 |
| Solid Tumor | 1 |
| Advanced Solid Tumor | 1 |
| Metastatic Cancer | 1 |
Sponsors
lead sponsor per trialBy country register
A trial with sites in more than one country appears in each of those registers.
Related compounds
Questions about Vemurafenib trials
How many clinical trials are testing Vemurafenib?
14 current trials in our USA, France, Italy, Canada, South Korea, Australia, China, Germany, Spain, Brazil, Israel, Poland, Czechia, Turkey, Belgium, Denmark, Mexico, Japan, UK, Netherlands, Portugal, Taiwan and Singapore registers name Vemurafenib (also registered as RO5185426) as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.
Are Vemurafenib trials recruiting patients?
Yes. 7 of the 14 trials are recruiting: 2 with sites in USA, 1 with sites in France, 1 with sites in Italy, 2 with sites in Canada, 1 with sites in South Korea, 1 with sites in Australia, 3 with sites in China, 1 with sites in Germany, 1 with sites in Spain, 1 with sites in Brazil, 1 with sites in Israel, 1 with sites in Czechia, 1 with sites in Turkey, 1 with sites in Denmark, 1 with sites in UK, 1 with sites in Netherlands and 1 with sites in Portugal. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.
Who sponsors Vemurafenib clinical trials?
Hoffmann-La Roche (2), Pfizer (1), Genentech, Inc (1) and Shanghai Kechow Pharma, Inc (1), among 13 lead sponsors in total. The number in brackets is how many trials each organisation leads.
Is Vemurafenib licensed in Ireland?
Yes. The HPRA medicines list includes 1 single-substance product containing Vemurafenib, for example Zelboraf 240 mg film-coated tablets (Roche Registration GmbH). A licence does not mean a product is currently marketed or reimbursed; see each product's record.
Is there a Vemurafenib shortage?
Not in the lists we track: Vemurafenib has no entry in the EMA, FDA or German BfArM shortage registers as of their latest sync.
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 Vemurafenib works or whether it is effective, and it is not medical advice.
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 Vemurafenib works or whether it is effective. Each trial links to its own record so you can check it yourself.
- ClinicalTrials.gov (U.S. National Library of Medicine) ↗ Trial IDs, titles, intervention names and synonyms, phase, overall status, lead sponsor and conditions for every trial on this page
This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Vemurafenib (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.