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Compound · clinical trials

Vebreltinib clinical trials

Also listed in trial records as BoRuiTiNi
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 6 trials in our China register that name Vebreltinib as an intervention. Synced 25 Sep 2026
6Current trials
4Recruiting now
6Lead sponsors
1Country register
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards
At a glance

Vebreltinib is named as an intervention in 6 current clinical trials in our China register. 4 are recruiting patients now. The most common phase is Phase 2. The sponsor with the most trials is Avistone Biotechnology Co., Ltd (1). The most-studied condition is Non-Small-Cell Lung Cancer.

Trials by status

  • Recruiting467%
  • Not yet open117%
  • Active, closed117%

Trials by phase

  • Phase 2467%
  • Phase 1/2233%
01

Clinical trials of Vebreltinib

6 trials
StudyPhaseStatusLead sponsorRegisters
Vebreltinib Plus PLB1004 as the First-line Therapy for Patients With EGFRm+/MET+ Locally Advanced or Metastatic NSCLC.
NCT06574347 · ClinicalTrials.gov ↗ · Non-Small-Cell Lung Cancer
Phase 2 Recruiting Avistone Biotechnology Co., Ltd. China
Vebreltinib for Advanced or Metastatic CCS
NCT07153887 · ClinicalTrials.gov ↗ · Clear Cell Sarcoma (CCS)
Phase 2 Recruiting Second Affiliated Hospital, Zhejiang University, School of Medicine China
Phase Ib/II Study of Vebreltinib With Furmonertinib in NSCLC Patients With c-Met Amplification After EGFR-TKI Failure
NCT07087223 · ClinicalTrials.gov ↗ · Non Small Cell Lung Cancer NSCLC
Phase 1/2 Recruiting Peking University Cancer Hospital & Institute China
Vebreltinib Plus Furmonertinib in Patients With EGFR-mutated Advanced Non-small Cell Lung Cancer and High PD-L1 Expression
NCT07655622 · ClinicalTrials.gov ↗ · Non-Small-Cell Lung Cancer
Phase 1/2 Recruiting Second Affiliated Hospital of Nanchang University China
Vebreltinib Plus Chemotherapy as First-line Treatment for MET-overexpressing NSCLC
NCT07549061 · ClinicalTrials.gov ↗ · Lung Neoplasms
Phase 2 Not yet open Shanghai Chest Hospital China
Combination of Vebreltinib and Osimertinib in Patients with EGFR 21 L858R Mutation Advanced NSCLC
NCT06827145 · ClinicalTrials.gov ↗ · Non-Small-Cell Lung Cancer
Phase 2 Active, closed National Cancer Center, China China

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 Vebreltinib

4 conditions
Non-Small-Cell Lung Cancer3Clear Cell Sarcoma (CCS)1Lung Neoplasms1Non Small Cell Lung Cancer NSCLC1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Avistone Biotechnology Co., Ltd.1
National Cancer Center, China1
Second Affiliated Hospital of Nanchang University1
Second Affiliated Hospital, Zhejiang University, School of Medicine1
Shanghai Chest Hospital1
Peking University Cancer Hospital & Institute1
04

By country register

RegisterTrialsRecruiting
Clinical trials in China64

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

05

Related compounds

06

Questions about Vebreltinib trials

How many clinical trials are testing Vebreltinib?

6 current trials in our China register name Vebreltinib as a drug or biological intervention, as of the registry sync on 25 September 2026. Completed and withdrawn studies are not counted.

Are Vebreltinib trials recruiting patients?

Yes. 4 of the 6 trials are recruiting: 4 with sites in China. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Vebreltinib clinical trials?

Avistone Biotechnology Co., Ltd (1), National Cancer Center, China (1), Second Affiliated Hospital of Nanchang University (1) and Second Affiliated Hospital, Zhejiang University, School of Medicine (1), among 6 lead sponsors in total. 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 Vebreltinib 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 โ€” it is not written from memory, and nothing here describes how Vebreltinib 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 Vebreltinib (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 25 Sep 2026.

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 โ€” 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 โ€” we correct promptly and log it.