Active, not recruitingPhase 1NCT05364073
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
Studying Small cell lung cancer
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- ArriVent BioPharma, Inc.
- Principal Investigator
- Jamuna ThimmarayappaArriVent BioPharma
- Intervention
- Furmonertinib(drug)
- Enrollment
- 160 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2022 – 2026
Study locations (30)
- ArriVent Investigative Site, Prescott, Arizona, United States
- ArriVent Investigative Site, Sacramento, California, United States
- ArriVent Investigative Site, Whittier, California, United States
- ArriVent Investigative Site, Celebration, Florida, United States
- ArriVent Investigative Site, Detroit, Michigan, United States
- ArriVent Investigative Site, Houston, Texas, United States
- ArriVent Investigative Site, Fairfax, Virginia, United States
- ArriVent Investigative Site, Blacktown, New South Wales, Australia
- ArriVent Investigative Site, St Leonards, New South Wales, Australia
- ArriVent Investigative Site, Heidelberg, Victoria, Australia
- Arrivent Investigative Site, Edmonton, Canada
- Arrivent Investigative Site, Toronto, Canada
- Allist Investigative Site, Hefei, Anhui, China
- Allist Investigative Site, Beijing, Beijing Municipality, China
- Allist Investigative Site, Chaoyang, Beijing Municipality, China
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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