RecruitingPhase 3NCT04853342
To Assess the Efficacy and Safety of Furmonertinib Versus Placebo, in Patients With Epidermal Growth Factor Receptor Mutation Positive Stage II-IIIA Non-small Cell Lung Carcinoma, Following Complete Tumour Resection With or Without Adjuvant Chemotherapy
Studying NON RARE IN EUROPE: Non-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
- Allist Pharmaceuticals, Inc.
- Principal Investigator
- Jianxing He, PHD, MDThe First Affiliated Hospital of Guangzhou Medical University
- Intervention
- Drug: Furmonertinib 80 mg(drug)
- Enrollment
- 318 enrolled
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2021 – 2030
Study locations (1)
- First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China
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.
Open NCT04853342 on ClinicalTrials.govOther trials for NON RARE IN EUROPE: Non-small cell lung cancer
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