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Efficacy and Safety of Glumetinib in patients with MET alteration NSCLC: a Multicenter, observational Real World Study based on digital follow-up

Efficacy and Safety of Glumetinib in patients with MET alteration NSCLC: a Multicenter, observational Real World Study based on digital follow-up

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400080439
Enrollment
Unknown
Registered
2024-01-29
Start date
2024-02-01
Completion date
Unknown
Last updated
2024-05-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-small cell lung cancer

Interventions

MET exon 14 skipping mutations:Observational study, not applicable
MET gene amplification:Observational study, not applicable
MET protein overexpression:Observational study, not applicable

Sponsors

Beijing Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Patient was aged = 18 years; 2) Patients were histologically or cytologically confirmed locally advanced or metastatic NSCLC (stage III-IV) and were not suitable to receive radical resection or chemoradiotherapy; 3) Patient had MET alteration(METex14 skipping, MET gene amplification and MET protein overexpression); 4) Patients who had started glumetinib treatment before before entering this trial; 5) Subjects fully understand and volunteered to participate in this study and had good compliance to follow-up

Exclusion criteria

Exclusion criteria: 1) Known intolerance or allergy to study drug; 2) Involved in other interventional clinical trials at the same time; 3) Patients were undergoing anti-cancer treatment with unmarketed drugs in China; 4) Combined with other malignant tumors and required to treatment; 5) Unsuitable subjects for this study determined by the investigator 6) pregnant or breast-feeding patients.

Design outcomes

Primary

MeasureTime frame
Time to treatment discontinuation;

Secondary

MeasureTime frame
Safety;Real world response rate;Real world disease control rate;Real world progression-free survival;Overall survival;

Countries

China

Contacts

Public ContactJun Zhao

Beijing Cancer Hospital

ohjerry@163.com+86 10 8819 6456

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026