Lung Cancer Clinical Trial

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)

Summary

Global, Phase 3, randomized, multicenter, open-label study evaluating the efficacy and safety of furmonertinib 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.

View Eligibility Criteria

Eligibility Criteria

Key Inclusion Criteria:

Histologically or cytologically documented, locally advanced or metastatic non-squamous Non-Small Cell Lung Cancer (NSCLC) not amenable to curative surgery or radiotherapy.
Documented results of the presence of an Epidermal Growth Factor Receptor (EGFR) exon 20 insertion mutation in tumor tissue or blood from local or central testing.
No prior systemic anticancer therapy regimens received for locally advanced or metastatic Non-Small Cell Lung Cancer (NSCLC) including prior treatment with any Epidermal Growth Factor Receptor (EGFR)-targeting agents (e.g., previous (EGFR) TKIs, monoclonal antibodies, or bispecific antibodies).
Patients who have received prior neo-adjuvant and/or adjuvant chemotherapy, immunotherapy, or chemo radiotherapy for non-metastatic disease (excluding EGFR-TKIs) must have experienced a treatment free interval of at least 12 months.
Patients with a history of treated CNS metastases or new asymptomatic CNS metastases are eligible.

Study is for people with:

Lung Cancer

Phase:

Phase 3

Estimated Enrollment:

375

Study ID:

NCT05607550

Recruitment Status:

Recruiting

Sponsor:

ArriVent BioPharma, Inc.

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There are 167 Locations for this study

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Arrivent Investigative Site
Daphne Alabama, 36526, United States More Info
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Yuma Arizona, 85364, United States
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Fayetteville Arkansas, 72703, United States
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Beverly Hills California, 90212, United States
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Fullerton California, 92835, United States
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Long Beach California, 90806, United States
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Los Alamitos California, 90720, United States
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Napa California, 94558, United States
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Orange California, 90868, United States
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Orange California, 92868, United States
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Sacramento California, 95817, United States More Info
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San Diego California, 92123, United States
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Santa Barbara California, 93105, United States
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Santa Monica California, 90404, United States More Info
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Santa Rosa California, 95403, United States
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Whittier California, 90602, United States
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Hartford Connecticut, 06102, United States
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Norwich Connecticut, 06360, United States
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Fort Myers Florida, 33901, United States More Info
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Saint Petersburg Florida, 33705, United States More Info
Arrivent Investigative Site
The Villages Florida, 32159, United States
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Peoria Illinois, 61615, United States
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Rolling Meadows Illinois, 60008, United States
Arrivent Investigative Site
Fort Wayne Indiana, 46804, United States
Arrivent Investigative Site
Indianapolis Indiana, 46250, United States
Arrivent Investigative Site
South Bend Indiana, 46601, United States
Arrivent Investigative Site
Bethesda Maryland, 20817, United States
Arrivent Investigative Site
Frederick Maryland, 21702, United States
Arrivent Investigative Site
Rockville Maryland, 20850, United States
Arrivent Investigative Site
Fairhaven Massachusetts, 02719, United States
Arrivent Investigative Site
Lansing Michigan, 48912, United States
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Bolivar Missouri, 65613, United States
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Kansas City Missouri, 64111, United States
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Saint Joseph Missouri, 64507, United States
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Saint Louis Missouri, 63110, United States
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Omaha Nebraska, 68114, United States More Info
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Belleville New Jersey, 07109, United States
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Englewood New Jersey, 07631, United States
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Florham Park New Jersey, 07932, United States
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Bronx New York, 10461, United States More Info
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Goldsboro North Carolina, 27534, United States
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Canton Ohio, 44708, United States
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Cincinnati Ohio, 45220, United States
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Cleveland Ohio, 44195, United States
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Columbus Ohio, 43214, United States
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Oklahoma City Oklahoma, 74146, United States
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Tulsa Oklahoma, 74146, United States
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Salem Oregon, 97301, United States
Arrivent Investigative Site
Gettysburg Pennsylvania, 17325, United States
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York Pennsylvania, 17403, United States
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Greenville South Carolina, 29607, United States
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Sioux Falls South Dakota, 57117, United States
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Memphis Tennessee, 38120, United States
ArriVent Investigative Site
Nashville Tennessee, 37203, United States More Info
ArriVent I
Contact
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Abilene Texas, 79606, United States More Info
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Houston Texas, 77030, United States
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Plano Texas, 75093, United States More Info
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Ogden Utah, 84405, United States
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Salt Lake City Utah, 84106, United States
ArriVent Investigative Site
Fairfax Virginia, 22031, United States More Info
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Fredericksburg Virginia, 22408, United States
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Bellingham Washington, 98225, United States
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Spokane Valley Washington, 99216, United States
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Tacoma Washington, 98405, United States
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Appleton Wisconsin, 54911, United States
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Blacktown , 2148, Australia More Info
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St Leonards , NSW 2, Australia More Info
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Woolloongabba , 4102, Australia More Info
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Salvador Bahia, 40170, Brazil More Info
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Belo Horizonte Minas Gerais, 30130, Brazil More Info
ArriVent Investigative Site
Rio De Janeiro RJ, 20231, Brazil More Info
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Pelotas RS, 96020, Brazil More Info
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São José Do Rio Preto Sao Paulo, 15090, Brazil More Info
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São Paulo Sao Paulo, 01321, Brazil More Info
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Blumenau SC Cep, 89015, Brazil More Info
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Liberdade São Paulo/SP, 01509, Brazil More Info
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Taubaté Taubate SP, 12030, Brazil More Info
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Porto Alegre , 91350, Brazil More Info
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Xuhui Hai City, 20003, China More Info
ArriVent Site
Contact
[email protected]
Allist Investigative Site
Zhengzhou Henan, 45005, China More Info
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Weihai Lingang Economic And Technological Development Zo, 26420, China More Info
ArriVent
Contact
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ArriVent Investigative Site
Meijiang Meizhou City, Guangdong Province, 51400, China More Info
Allist
Anyang , 45500, China More Info
Allist Investigative Site
Changchun , 13000, China More Info
156021
Contact
[email protected]
Allist Investigative Site
Changsha , 41000, China More Info
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Changsha , 41003, China More Info
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Chengdu , 61004, China More Info
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Chenzhou , 42309, China More Info
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Chongqing , 40003, China More Info
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Guangzhou , 51006, China More Info
Site 156044
Contact
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Allist Investigative Site
Guangzhou , 51028, China More Info
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Harbin , 15008, China More Info
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Hefei , 23008, China More Info
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Huai'an , 22330, China More Info
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Huizhou , 51600, China More Info
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Jinan , 25001, China More Info
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Jinan , 25011, China More Info
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Jining , 27200, China More Info
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Lanzhou , 73003, China More Info
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Lishui , 32302, China More Info
Allist
Luoyang , 47100, China More Info
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Nanchang , 33000, China More Info
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Nanchang , 33004, China More Info
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Nanjing , 21000, China More Info
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Ningbo , 31504, China More Info
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Shanghai , 20003, China More Info
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Shanghai , 20043, China More Info
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Shantou , 51503, China More Info
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Shenyang , 11004, China More Info
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Shenzhen , 51800, China More Info
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Taiyuan , 03000, China More Info
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Taoyuan , 30000, China More Info
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Tianjin , 30006, China More Info
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Weihui , 45300, China More Info
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Wuhan , 43002, China More Info
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Xiamen , 36100, China More Info
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Xianyang , 44113, China More Info
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Xinxiang , 45300, China More Info
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Xuzhou , 22100, China More Info
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Zhengzhou , 45000, China More Info
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Caen , 14000, France More Info
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Lyon , 69003, France More Info
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Lyon , 69008, France More Info
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Marseille , 13915, France More Info
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Toulouse , 31059, France More Info
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Villejuif , 94800, France More Info
ArriVent Investigative Site
Rozzano Milan, 20089, Italy More Info
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Contact
[email protected]
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Meldola , 47014, Italy More Info
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Akashi , 673-8, Japan More Info
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Hirakata , 573-1, Japan More Info
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Kashiwa , 277-8, Japan More Info
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Nagoya , 460-0, Japan More Info
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Sapporo-shi , 003-0, Japan More Info
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Sendai , 980-0, Japan More Info
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Shizuoka , 41187, Japan More Info
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Tokyo , 113-8, Japan More Info
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Ube , 755-0, Japan More Info
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Yokohama , 241-8, Japan More Info
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Ōsaka-sayama , 589-8, Japan More Info
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Busan , 49241, Korea, Republic of More Info
Arrivent Investigative Site
Hwasun , 58128, Korea, Republic of More Info
Arrivent Investigative Site
Seoul , 2447, Korea, Republic of More Info
Arrivent Investigative Site
Seoul , 3722, Korea, Republic of More Info
Arrivent Investigative Site
Seoul , 5505, Korea, Republic of More Info
Arrivent Investigative Site
Seoul , 6351, Korea, Republic of More Info
ArriVent Investigative Site
George Town Pulau Pinang, 10990, Malaysia More Info
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Contact
[email protected]
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Cheras , 56000, Malaysia More Info
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Kota Bharu , 15586, Malaysia More Info
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Kuala Lumpur , 50586, Malaysia More Info
Arrivent Investigative Site
Kuching , 93586, Malaysia More Info
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Amsterdam , 1066 , Netherlands More Info
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Harderwijk , 3844D, Netherlands More Info
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Cebu , 6000, Philippines More Info
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Davao City , 8000, Philippines More Info
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Pasig , 1600, Philippines More Info
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Singapore , 16961, Singapore More Info
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A Coruña , 15006, Spain More Info
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Barcelona , 08035, Spain More Info
ArriVent Investigative Site
Madrid , 28020, Spain More Info
ArriVent Site
Contact
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Valencia , 46026, Spain More Info
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Chang Hua , 50006, Taiwan More Info
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Kaohsiung , 807, Taiwan More Info
ArriVent Investigative Site
Kaohsiung , 82445, Taiwan More Info
ArriVent Site
Contact
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ArriVent Investigative Site
Taichung , 40721, Taiwan More Info
ArriVent Site
Contact
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Arrivent Investigative Site
Tainan , 704, Taiwan More Info
Arrivent Investigative Site
Taipei , 10048, Taiwan More Info
Arrivent Investigative Site
Bangkok , 10210, Thailand More Info
Arrivent Investigative Site
Bangkok , 10330, Thailand More Info
Arrivent Investigative Site
Bangkok , 10400, Thailand More Info
Arrivent Investigative Site
Hat Yai , 90110, Thailand More Info

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 3

Estimated Enrollment:

375

Study ID:

NCT05607550

Recruitment Status:

Recruiting

Sponsor:


ArriVent BioPharma, Inc.

How clear is this clinincal trial information?

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