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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)

← catalyst calendar

NCT05607550

Sponsored by ArriVent BioPharma, Inc. (industry) · AVBP — their whole pipeline →. With Allist Pharmaceuticals, Inc..

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
398actual
Sites
208
Countries
Australia, Brazil, Canada +16

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-06-01actualWhen the study began enrolling
Primary completion2025-08-15estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-02-15estimatedThe whole study's end, after follow-up
First posted2022-11-07actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-06-22actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Metastatic Non-Small Cell Lung Cancer
  • Advanced Non-Small Cell Lung Cancer
  • EGFR Exon 20 Mutations

Interventions

  • Drug: furmonertinib 240 mg oral, daily — also filed as AST2818
  • Drug: furmonertinib 160 mg oral, daily — also filed as AST2818
  • Drug: platinum-based chemotherapy

Primary outcome

what the primary-completion date above is the date OF
Progression Free Survival (PFS) determined by blinded independent central review (BICR)
measured Up to 32 months after first dose

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