CI

At a glance

ClinicalIndex Comparison Record
Phase 2Not Yet Recruiting· 91 target
Drug / intervention
gumarontinib +1 moredrug
Likely dose
gumarontinib 300 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06452433
NCT06452433Phase 2Not Yet Recruiting

Gumarontinib Combined With Third-generation EGFR-TKI in Patients With Locally Advanced or Metastatic Non-small Cell Lung Cancer With MET Amplification Following EGFR-TKI Treatment Failure.

Cancer Institute and Hospital, Chinese Academy of Medical Sciences·interventional·Posted Jun 11, 2024·Updated Jun 11, 2024

In Brief

A Phase 2 clinical trial evaluating gumarontinib and third-generation EGFR-TKI (Osimertinib, Almonertinib or Furmonertinib) for Non-small Cell Lung Cancer. Not yet recruiting, targeting 91 participants.

Detailed Summary

This study evaluated the efficacy and safety of gumarontinib combined with third-generation EGFR-TKI in the treatment of locally advanced or metastatic NSCLC with MET amplification after first-line EGFR-TKI failure, without limiting the type of third-generation EGFR-TKI. The study was divided into 2 cohorts: Cohort 1 included patients with MET amplification after third-generation EGFR-TKI first-line therapy resistance, and cohort 2 included patients with MET amplification after first-generation EGFR-TKI first-line therapy resistance.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--
Collaborators--

Timeline

Phase 2Not Yet Recruiting
2025202620272028
First PostedJun 11, 2024
Enrollment StartJun 1, 2024
Primary CompletionDec 12, 2027
Study CompletionFeb 2, 2028
TodayJul 1, 2026
Enrollment to primary: 3.5 yearsPosted 2.1 years agoPrimary completion in 1.4 years

Interventions

gumarontinibdrug

300 mg , qd ,po, expect 6 months.

third-generation EGFR-TKI (Osimertinib, Almonertinib or Furmonertinib)drug

According to the actual situation of patients. Take as recommended, expect 6 months.