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vemurafenib

Generic: VEMURAFENIB·Brand: ZELBORAF, Zelboraf

vemurafenib: 7 clinical trials tracked.

vemurafenib evidence translation

What we can confirm

7 tracked trials

No verified listed developer

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about vemurafenib, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence5 indications · 4 study sponsors
Clinical Trials (7)

Optimization of the Time and Dosage of Vemurafenib in BRAF Positive Juvenile Patients With Refractory Histiocytosis

NCT04943198·Phase 2
Recruiting

Primary endpoint: event-free survival

InterventionalRandomizedopen25 targetStarted 2021-04Completion 2027-061 site · PolandAnna Raciborska

NAUTIKA1: A Multicenter, Phase II, Neoadjuvant and Adjuvant Study of Multiple Therapies in Biomarker-selected Patients With Resectable Stages IB-III Non-small Cell Lung Cancer

NCT04302025·Phase 2·MRUS
Recruiting

Primary endpoint: Tyrosine Kinase Inhibitor (TKI) Cohort: Proportion of Participants With Major Pathologic Response (MPR)

Interventionalopen99 targetStarted 2020-11Completion 2030-0538 sites · United StatesGenentech, Inc.

An Open Label, Multicenter Extension Study in Patients Previously Enrolled in a Genentech and/or F. Hoffmann-La Roche Ltd Sponsored Atezolizumab Study (IMbrella B)

NCT03768063·Phase 3·KYNB
Active, not recruiting

Primary endpoint: Number of Participants With Continued Access to Atezolizumab-Based Therapy and/or Comparator Agent(s)

Interventionalopen1,000 targetStarted 2019-02Completion 2028-0750 sites · Australia, Belgium, Brazil, Bulgaria…Hoffmann-La Roche

Phase II Trial of BRAF/MEK Inhibitors in Papillary Craniopharyngiomas

NCT03224767·Phase 2·CGON
Active, not recruiting

Primary endpoint: Response Rate

Interventionalopen24 targetStarted 2018-01Completion 2028-0850 sites · United StatesAlliance for Clinical Trials in Oncology

Phase I Study of Escalating Doses of XL888 With Vemurafenib Plus Cobimetinib for Patients With Unresectable BRAF Mutated Stage III/IV Melanoma

NCT02721459·Phase 1
Active, not recruiting

Primary endpoint: Maximum Tolerated Dose (MTD)

Interventionalopen26 targetStarted 2016-09Completion 2026-111 site · United StatesH. Lee Moffitt Cancer Center and Research Institute

Targeted Agent and Profiling Utilization Registry (TAPUR) Study

NCT02693535·Phase 2·CGON
Recruiting

Primary endpoint: Objective Response Rate defined as % of participants in a cohort with complete or partial response or with stable disease according to standard response criteria

Interventionalopen4,200 targetStarted 2016-03Completion 2028-1250 sites · United StatesAmerican Society of Clinical Oncology

A Phase II Clinical Trial of Vemurafenib With Lymphodepletion Plus Adoptive Cell Transfer and High Dose IL-2 in Patients With Metastatic Melanoma

NCT01659151·Phase 2·FLNA
Completed

Primary endpoint: Percentage of Participants With Overall Response (OR)

Interventionalopen17 enrolledStarted 2012-08Completion 2025-081 site · United StatesH. Lee Moffitt Cancer Center and Research Institute