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

38 Participants
are divided into 1 treatment group

Locations

1
National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China

Sponsors and collaborators

Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Lead sponsor

Alpha Biopharma (Jiangsu) Co., Ltd.

Collaborator