TrialSignal
Clinical trial intelligence report
Clinical Activity of Icotinib in Patients With Advanced Non-small-cell Lung Cancer Harbouring Uncommon EGFR Mutations: a Single-arm, Prospective, Phase 2 Study
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 20, 2026
NCT ID
NCT02961270
Status
UNKNOWN
Phase
Phase 2
Sponsor
Chinese Academy of Medical Sciences
Executive brief
Investment-Ready Snapshot
Icotinib, a first-generation EGFR TKI, is being evaluated in a targeted population of advanced non-small cell lung cancer (NSCLC) patients with uncommon EGFR mutations. This study addresses a significant unmet need in the NSCLC market, particularly as existing therapies primarily target common mutations (e.g., 19 del and 21 L858R). The potential efficacy of icotinib in this niche could position it favorably against competitors, especially in regions where access to newer agents is limited. Given the estimated enrollment of 30 patients and the focus on a specific mutation profile, the results could provide critical insights into the drug's viability and market potential, particularly in Asian markets where icotinib is already established.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT02961270
Indication
Non-small Cell Lung Cancer
Modality
small molecule
Target
Epidermal Growth Factor Receptor (EGFR) with a focus on uncommon mutations
Intervention
Icotinib
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.