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NCT07298148

Firmonertinib 160 mg in Patients With EGFR-Mutant Advanced NSCLC Demonstrating SD After 8 Week Induction With Firmonertinib 80 mg

Not yet recruiting Phase 2 Last updated 21 January 2026
What this trial tests

Phase 2 trial testing Firmonertinib 160mg in NSCLC Stage IV in 28 participants. Not yet recruiting.

Timeline
1 January 2026
Primary endpoint
31 December 2030
31 December 2032

Quick facts

Lead sponsorPeking University Cancer Hospital & Institute
PhasePhase 2
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment28
Start date1 January 2026
Primary completion31 December 2030
Estimated completion31 December 2032

Drugs / interventions tested

Conditions studied

Sponsor

Peking University Cancer Hospital & Institute

Who can join

Adults 18 to 75, any sex, with NSCLC Stage IV or EGFR Positive Non-small Cell Lung Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study evaluates the efficacy and safety of Firmonertinib 160 mg once daily in patients with EGFR-mutant, advanced NSCLC who achieve stable disease after first-line Firmonertinib 80 mg for 8 weeks.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for NSCLC Stage IV

Currently open trials in the same condition.

Other Peking University Cancer Hospital & Institute trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07298148.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing