Neoadjuvant Furmonertinib Plus Bevacizumab or Furmonertinib Monotherapy for Resectable and Potentially Resectable Stage III-IVA EGFR Mutation-Positive Lung Adenocarcinoma

Trial Details

NCT ID

NCT05503667

Phase

PHASE2

Sponsor

Shanghai Pulmonary Hospital, Shanghai, China

Status

RECRUITING

Cancer Type

Adenocarcinoma Lung Cancer

Interventions

• Furmonertinib
• Bevacizumab

Locations (sample)

• Shanghai, Shanghai Municipality, China|31.22222,121.45806

Key Eligibility Criteria

• Lung adenocarcinoma patient with EGFR sensitive mutation as confirmed by needle biopsy;
• At stage III-IVA (TNM Staging, Version 8) as identified by chest CT, PET-CT or/and EBUS;
• No systemic metastasis (confirmed by head MRI, whole body bone scan, PET-CT, liver and adrenal CT, etc.);
• With the feasiblility or potential feasibility to receive radical surgery (radical lung lobectomy+systematic lymph node dissection);

For full eligibility, visit ClinicalTrials.gov.

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