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Active, not recruiting Phase 3 Interventional

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)

ClinicalTrials.gov ID: NCT05607550

Public ClinicalTrials.gov record NCT05607550. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 16, 2026, 3:58 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Global, Phase 3, Randomized, Multicenter, Open-Label Study to Investigate the Efficacy and Safety of Furmonertinib Compared to Platinum-Based Chemotherapy as First-Line Treatment for Patients With Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) With Epidermal Growth Factor Receptor (EGFR) Exon 20 Insertion Mutations (FURVENT)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Global, Phase 3, randomized, multicenter, open-label study evaluating the efficacy and safety of furmonertinib (firmonertinib) at 2 dose levels (160 mg once daily \[QD\] and 240 mg QD) compared to platinum-based chemotherapy in previously untreated patients with locally advanced or metastatic non-squamous Non-Small Cell Lung Cancer (NSCLC) with Epidermal Growth Factor Receptor (EGFR) exon 20 insertion mutations. A target of approximately 375 patients will be randomized in a 1:1:1 ratio to treatment with furmonertinib 240 mg QD, furmonertinib 160 mg QD, or platinum-based chemotherapy.

Study identification

NCT ID
NCT05607550
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
ArriVent BioPharma, Inc.
Industry
Enrollment
398 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 1, 2023 (Actual)
Primary completion
Aug 15, 2025 (Estimated)
Completion
Feb 15, 2028 (Estimated)
Last update posted
Jun 22, 2025

2023 – 2028

United States locations

U.S. sites
69
U.S. states
28
U.S. cities
67
Facility City State ZIP Site status
Arrivent Investigative Site Daphne Alabama 36526 —
Arrivent Investigative Site Yuma Arizona 85364 —
Arrivent Investigative Site Fayetteville Arkansas 72703 —
Arrivent Investigative Site Beverly Hills California 90212 —
Arrivent Investigative Site Fullerton California 92835 —
Arrivent Investigative Site Long Beach California 90806 —
Arrivent Investigative Site Los Alamitos California 90720 —
Arrivent Investigative Site Napa California 94558 —
Arrivent Investigative Site Orange California 90868 —
Arrivent Investigative Site Orange California 92868 —
Arrivent Investigative site Sacramento California 95817 —
Arrivent Investigative Site San Diego California 92123 —
Arrivent Investigative Site Santa Barbara California 93105 —
Arrivent Investigative Site Santa Monica California 90404 —
Arrivent Investigative Site Santa Rosa California 95403 —
Arrivent Investigative Site Whittier California 90602 —
Arrivent Investigative Site Hartford Connecticut 06102 —
Arrivent Investigative Site Norwich Connecticut 06360 —
Arrivent Investigative Site Fort Myers Florida 33901 —
Arrivent Investigative Site St. Petersburg Florida 33705 —
Arrivent Investigative Site The Villages Florida 32159 —
Arrivent Investigative Site Peoria Illinois 61615 —
Arrivent Investigative Site Rolling Meadows Illinois 60008 —
Arrivent Investigative Site Fort Wayne Indiana 46804 —
Arrivent Investigative Site Indianapolis Indiana 46250 —
Arrivent Investigative Site South Bend Indiana 46601 —
Arrivent Investigative Site Bethesda Maryland 20817 —
Arrivent Investigative Site Frederick Maryland 21702 —
Arrivent Investigative Site Rockville Maryland 20850 —
Arrivent Investigative Site Fairhaven Massachusetts 02719 —
Arrivent Investigative Site Lansing Michigan 48912 —
Arrivent Investigative Site Bolivar Missouri 65613 —
Arrivent Investigative Site Kansas City Missouri 64111 —
Arrivent Investigative Site Saint Joseph Missouri 64507 —
Arrivent Investigative Site St Louis Missouri 63110 —
Arrivent Investigative Site Omaha Nebraska 68114 —
Arrivent Investigative Site Belleville New Jersey 07109 —
Arrivent Investigative Site Englewood New Jersey 07631 —
Arrivent Investigative Site Florham Park New Jersey 07932 —
Arrivent Investigative Site The Bronx New York 10461 —
Arrivent Investigative Site Goldsboro North Carolina 27534 —
ArriVent Investigative Site Pinehurst North Carolina 28374 —
Arrivent Investigative Site Canton Ohio 44708 —
Arrivent Investigative Site Cincinnati Ohio 45220 —
ArriVent Investigative Site Cincinnati Ohio 45242 —
Arrivent Investigative Site Cleveland Ohio 44195 —
Arrivent Investigative Site Columbus Ohio 43214 —
Arrivent Investigative Site Oklahoma City Oklahoma 73102 —
Arrivent Investigative Site Tulsa Oklahoma 74146 —
Arrivent Investigative Site Salem Oregon 97301 —
Arrivent Investigative Site Gettysburg Pennsylvania 17325 —
ArriVent Investigative Site Langhorne Pennsylvania 19047 —
Arrivent Investigative Site York Pennsylvania 17403 —
Arrivent Investigative Site Greenville South Carolina 29607 —
Arrivent Investigative Site Sioux Falls South Dakota 57117 —
Arrivent Investigative Site Memphis Tennessee 38120 —
ArriVent Investigative Site Nashville Tennessee 37203 —
Arrivent Investigative Site Abilene Texas 79606 —
ArriVent Investigative Site Austin Texas 78745 —
Arrivent Investigative Site Houston Texas 77030 —
Arrivent Investigative Site Plano Texas 75093 —
Arrivent Investigative Site Ogden Utah 84405 —
Arrivent Investigative Site Salt Lake City Utah 84106 —
ArriVent Investigative Site Fairfax Virginia 22031 —
Arrivent Investigative Site Fredericksburg Virginia 22408 —
Arrivent Investigative Site Bellingham Washington 98225 —
Arrivent Investigative Site Spokane Valley Washington 99216 —
Arrivent Investigative Site Tacoma Washington 98405 —
Arrivent Investigative Site Appleton Wisconsin 54911 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 139 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05607550, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 22, 2025 · Synced Oct 16, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05607550 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →