Overview
Clinical Study of Utidelone Injection in Patients With Advanced Non-small Cell Lung Cancer(NSCLC)
Status:
Recruiting
Recruiting
Trial end date:
2021-09-30
2021-09-30
Target enrollment:
0
0
Participant gender:
All
All
Summary
To assess the effectiveness and safety of utidelone injection in patients with advanced or metastatic NSCLC as a phase II trialPhase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Beijing Biostar Technologies, LtdCollaborator:
Chengdu Biostar Pharmaceuticals, Ltd
Criteria
Inclusion Criteria:1. Histologically or cytologically confirmed non-small cell lung cancer
2. NSCLC patients who are not suitable for surgery or radical radiotherapy or
chemotherapy, or who have failed to or are intolerable for standard treatment in local
advanced or metastatic NSCLC;
3. NSCLC patients failed or intolerable to previous standard second-line treatment
(including platinum chemotherapy or targeted therapy);
4. Patients who did not receive chemotherapy, radiotherapy, surgical therapy, molecularly
targeted drug therapy, or immunotherapy 4 weeks prior to enrollment;
5. Age 18 -70 years old, ECOG performance status of 0-1; Life expectancy of 3 months or
more;
6. Patients must have measurable disease, defined as at least one target lesion that can
be accurately measured by imaging techniques in at least one dimension as ≥20 mm with
conventional computed tomography (CT), ≥10 mm with spiral CT scan (≥15mm for lymph
node) within 3 weeks before enrolment;
7. Patients with no brain metastases or with brain metastases but are stable for more
than 4 weeks after treatment;
8. Peripheral neuropathy (PN)
9. Patients must have normal haematology as defined below: HGB ≥9 g/L, absolute
neutrophil count ≥1.5×109/L, platelets ≥80×109/L, bilirubin ≤1.5× the upper limit of
normal (ULN) (patients with liver metastasis ≤3xULN), aspartate transaminase (AST)/
alanine transaminase (ALT) ≤2.5 ×ULN (patients with liver metastasis ≤5xULN), and
creatinine clearance ≥45 mL/min;
10. Patients with no major organ dysfunctions and heart disease;
11. Patients who give written informed consent with good compliance.
Exclusion Criteria:
1. Patients who are pregnant or breast feeding;
2. Patients with active tuberculosis
3. Patients with high possibility of interstitial lung disease ;
4. Patients with comorbidities, such as carcinomatous meningitis, central nervous system
(CNS) metastasis, other active malignancies requiring simultaneous treatment, but not
including cervical cancer in situ or basal cell carcinoma of the skin, severe
disorders of the heart, lung, liver, or kidneys, severe hypertension, uncontrolled
diabetes, severe gastrointestinal ulceration, active infections in need of
antibiotics, or with incontrollable psychiatric history;
5. patients with HIV, untreated active hepatitis;
6. Patients with poor compliance;
7. Patients not fitted for this study determined by the investigators.