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Therapy Name | Furmonertinib |
Synonyms | |
Therapy Description |
Furmonertinib (alflutinib) is a third-generation EGFR inhibitor that targets both EGFR activating mutations and T790M, potentially leading to tumor growth inhibition (PMID: 33780662, PMID: 35662408). |
Drug Name | Trade Name | Synonyms | Drug Classes | Drug Description |
---|---|---|---|---|
Furmonertinib | AST2818|AST2818|Alflutinib | EGFR Inhibitor 3rd gen 26 | Furmonertinib (alflutinib) is a third-generation EGFR inhibitor that targets both EGFR activating mutations and T790M, potentially leading to tumor growth inhibition (PMID: 33780662, PMID: 35662408). |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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NCT05607550 | Phase III | Cisplatin + Pemetrexed Disodium Furmonertinib Carboplatin + Pemetrexed Disodium | Study to Compare Furmonertinib to Platinum-Based Chemotherapy for Patients With Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) With Epidermal Growth Factor Receptor (EGFR) Exon 20 Insertion Mutations (FURVENT) | Recruiting | USA | NLD | ITA | ISR | GBR | FRA | ESP | CAN | BRA | AUS | 9 |
NCT05364073 | Phase I | Furmonertinib | Study of Furmonertinib in Patients With Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) With Activating, Including Uncommon, Epidermal Growth Factor Receptor (EGFR) or Human Epidermal Growth Factor Receptor 2 (HER2) Mutations | Active, not recruiting | USA | NLD | ITA | GBR | FRA | ESP | CAN | AUS | 3 |