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

NCT ID: NCT04853342

Last Updated: 2025-04-04

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE3
• Total Enrollment: 318 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-06-07
• Study Completion Date: 2030-01-31

Brief Summary

This is a phase 3 double-blind, randomized, placebo-controlled, study to assess the efficacy and safety of Furmonertinib (AST2818) versus placebo in patients with stage II-IIIA non-small cell lung cancer (NSCLC) with centrally confirmed, most common sensitising EGFR mutations (Ex19Del and L858R) either alone or in combination with other EGFR mutations as confirmed by a central test, who have had complete tumour resection, with or without postoperative adjuvant chemotherapy.

Conditions

Non-small Cell Lung Carcinoma

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Furmonertinib

Furmonertinib (80 mg orally, once daily), in accordance with the randomization schedule.

Group Type: EXPERIMENTAL

Drug: Furmonertinib 80 mg

Intervention Type: DRUG

The initial dose of Furmonertinib 80 mg once daily

Placebo Furmonertinib

Matching placebo for Furmonertinib (80 mg orally, once daily), in accordance with the randomization schedule.

Group Type: PLACEBO_COMPARATOR

Furmonertinib 80 mg placebo

Intervention Type: DRUG

The initial dose of Furmonertinib 80 mg once daily

Interventions

Drug: Furmonertinib 80 mg

The initial dose of Furmonertinib 80 mg once daily

Intervention Type: DRUG

Furmonertinib 80 mg placebo

The initial dose of Furmonertinib 80 mg once daily

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Male or female, aged at least 18 years.
• Histologically confirmed diagnosis of primary non-small lung cancer (NSCLC) on predominantly non-squamous histology.
• MRI or CT scan of the brain must be done prior to surgery as it is considered standard of care.
• Patients must be classified post-operatively as Stage IB, II, or IIIA on the basis of pathologic criteria.
• Confirmation by the central laboratory that the tumor harbors one of the 2 common EGFR mutations known to be associated with EGFR-TKI sensitivity (Ex19del, L858R), either alone or in combination with other EGFR mutations including T790M.
• Complete surgical resection of the primary NSCLC is mandatory. All gross disease must have been removed at the end of surgery. All surgical margins of resection must be negative for the tumor.
• Complete recovery from surgery and standard post-operative therapy (if applicable) at the time of randomization.
• World Health Organization Performance Status of 0 to 1.
• Female patients should be using adequate contraceptive measures, should not be breastfeeding, and must have a negative pregnancy test prior to the first dose of the study drug; or female patients must have evidence of non-child-bearing potential.

Exclusion Criteria

• Pre-operative or post-operative or planned radiation therapy for the current lung cancer
• Pre-operative (neo-adjuvant) platinum-based or other chemotherapy
• Any prior anticancer therapy
• Prior treatment with neoadjuvant or adjuvant EGFR-TKI at any time
• Major surgery (including primary tumor surgery, excluding placement of vascular access) within 4 weeks of the first dose of study drug
• Patients currently receiving medications or herbal supplements known to be potent inducers of cytochrome P450 (CYP) 3A4
• Treatment with an investigational drug within five half-lives of the compound or any of its related material.
• Patients who have had only segmentectomies or wedge resections
• History of other malignancies, except: adequately treated non-melanoma skin cancer, curatively treated in-situ cancer, or other solid tumors curatively treated with no evidence of disease for > 5 years following the end of treatment.
• Any unresolved toxicities from prior therapy greater than CTCAE Grade 1 at the time of starting study treatment with the exception of alopecia and Grade 2, prior platinum-therapy related neuropathy.
• Any evidence of severe or uncontrolled systemic diseases, including uncontrolled hypertension and active bleeding diatheses; or active infection including hepatitis B, hepatitis C, and human immunodeficiency virus (HIV).
• Refractory nausea and vomiting, chronic gastrointestinal diseases, inability to swallow the formulated product, or previous significant bowel resection that would preclude adequate absorption of AZD9291.
• Any of the following cardiac criteria:
• Mean resting corrected QT interval (QTc) >470 msec, obtained from 3 ECGs, using the screening clinic ECG Machine-derived QTc value.
• Any clinically important abnormalities in rhythm, conduction, or morphology of resting ECG.
• Any factors that increase the risk of QTc prolongation or risk of arrhythmic events, or unexplained sudden death under 40 years of age in first-degree relatives or any concomitant medication known to prolong the QT interval.
• Past medical history of ILD, drug-induced ILD, radiation pneumonitis which required steroid treatment, or any evidence of clinically active ILD.
• Inadequate bone marrow reserve or organ function.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Allist Pharmaceuticals, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jianxing He, PHD

Role: PRINCIPAL_INVESTIGATOR

The First Affiliated Hospital of Guangzhou Medical University

Locations

First Affiliated Hospital of Soochow University

Suzhou, Jiangsu, China

Site Status: RECRUITING

Countries

China

Central Contacts

Jianxing He, PHD

Role: CONTACT

drjianxing.he@gmail.com

020-83062114

Wenhua Liang, PHD

Role: CONTACT

liangwh1987@163.com

020-83062114

Facility Contacts

Hua Zhang

Role: primary

sdfyy8040@126.com

0512-67780040

Other Identifiers

ALSC010AST2818

Identifier Type: -

Identifier Source: org_study_id