About this trial
A Prospective Study of Zorifertinib Combined with Intra-Ommaya Reservoir Cerebrospinal Fluid Chemotherapy for Leptomeningeal Progression in NSCLC Patients After Third-Generation EGFR-TKI Therapy
Eligibility criteria
Qualifiers
1. Have fully understood the study and voluntarily signed the Informed Consent Form (ICF).
Neutrophil count ≥ 1.5 × 10⁹/L
Platelet count ≥ 100 × 10⁹/L
Hemoglobin ≥ 90 g/L
Disqualifiers
1. Subjects with a history of cranial or spinal radiotherapy within 6 months prior to study drug administration are ineligible for enrollment. Radiotherapy for bone metastases within 3 months prior to study drug administration is also not permitted.
Myocardial infarction within 6 months prior to screening;
Documented history of heart failure (NYHA Class III-IV);
Uncontrolled hypertension: systolic blood pressure ≥160 mmHg and/or diastolic blood pressure ≥100 mmHg, regardless of antihypertensive medication use (adjustment of antihypertensive drugs prior to screening is permitted);
Trial design
Treatments tested in this trial
- Zorifertinib Plus Intra-Ommaya CSF Chemotherapy
Treatment groups
Sponsors and collaborators
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Lead sponsor
Alpha Biopharma (Jiangsu) Co., Ltd.
Collaborator