A Study of BPI-7711 Capsule in Non-small Cell Lung Cancer Patients
About the study
A randomized, double-blind, positive controlled phase III study to evaluate the efficacy and safety of BPI-7711 capsule in locally advanced or recurrent/metastatic treatment-naïve non-small cell lung cancer patients with EGFR mutation
Who can take part
You may be eligible to participate in the study if you meet the following criteria:
INCLUSION CRITERIA
Inclusion Criteria:
- Histologically or cytologically confirmed non-small cell lung cancer.
- The ECOG score of performance status is 0-1.
- Locally advanced or recurrent metastatic NSCLC that has never received systemic treatment.
- According to RECIST1.1 criteria, there is at least 1 measurable lesion that has not been previously irradiated.
- Prior to enrollment, a central laboratory testing report has confirmed that the tumor has one of two common EGFR mutations positive that are sensitive to EGFR-TKI therapy, accompanied with or not accompanied with other EGFR mutation, with the exception of exon 20 insertion.
EXCLUSION CRITERIA
Exclusion Criteria:
- Previously received systemic treatment for locally advanced or recurrent metastatic cancer.
- Primary T790M mutation-positive patient.
- Previous interstitial lung disease, drug-induced interstitial lung disease, radiation pneumonia requiring hormonal therapy, or any clinically proven active interstitial lung disease.
- Known active infections such as hepatitis B, hepatitis C, and human immunodeficiency virus.
- Local radiation therapy is carried out within 1 week; more than 30% bone marrow radiation therapy or extensive radiation therapy is performed within 4 weeks.
- ≤ 4 weeks from major surgery or ≤ 2 weeks from minor surgery.
Study Locations
Enter your ZIP code/Postal code/PIN code to locate study sites near you:
How to Apply
Contact the study center to learn if this study is a good match for you.
Study’s details
Contition
NSCLC
Age (in years)
18+
Phase
Phase 3
Participants needed
369
Est. Completion Date
Feb 29, 2024
Treatment type
Interventional
Sponsor
Beta Pharma, Inc.
ClinicalTrials.gov identifier
NCT03866499
Study number
BPI-7711301
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