To Assess the Efficacy and Safety of Furmonertinib in Patients With Epidermal Growth Factor Receptor 20ins Mutation Positive Stage IB-IIIA Non-small Cell Lung Carcinoma, Following Complete Tumour Resection With or Without Adjuvant Chemotherapy

This is a phase II, prospective, multi-centre study. To assess the efficacy and safety of furmonertinib in patients with epidermal growth factor receptor 20ins mutation positive stage IB-IIIA Non-small Cell Lung Carcinoma, following complete tumour resection with or without adjuvant chemotherapy. The study plans to enroll 20 subjects, treating with furmonertinib 160mg/d, until disease recurrence, death or intolerability. The maximum duration of treatment is three years. The primary endpoint is DFS. The secondary endpoint include DFS rate , OS and the change of HRQoL. In addition, the periph

Trial Details

NCT ID

NCT06192849

Phase

PHASE2

Sponsor

Juan LI, MD

Status

RECRUITING

Cancer Type

Lung Cancer

Interventions

• Furmonertinib

Locations (sample)

• Chengdu, Sichuan, China|30.66667,104.06667

Key Eligibility Criteria

• Provide informed consent prior to any study specific procedures;
• Male or female, aged at least 18 years;
• Complete surgical resection of the primary NSCLC is mandatory. All gross disease must have been removed at the end of surgery. All surgical margins…
• Patients must be classified post-operatively as Stage IB, II, or IIIA on the basis of pathologic criteria;

For full eligibility, visit ClinicalTrials.gov.

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