Status:
COMPLETED
Phase II Study of Cabazitaxel-XRP6258 in Advanced Non-Small Cell Lung Cancer
Lead Sponsor:
University of Alabama at Birmingham
Collaborating Sponsors:
Sanofi
Conditions:
Non-small Cell Lung Cancer (NSCLC)
Stage IV NSCLC
Eligibility:
All Genders
19+ years
Phase:
PHASE2
Brief Summary
Lung cancer is the leading cause of cancer death worldwide and in the United States. The majority of lung cancers are non-small cell lung cancer (NSCLC). The majority of NSCLC cases are advanced at th...
Detailed Description
A substantial number of patients with lung cancer progress after first line treatment and require second line chemotherapy. Lung cancer appears to account for 40-50% of all known brain metastasis. The...
Eligibility Criteria
Inclusion
- Histologic or cytologic diagnosis of NSCLC (squamous or non-squamous or NSCLC-not specified)
- Subjects who have failed first line chemotherapy (platinum doublets or non- platinum doublets \[previous taxane exposure is allowed\]) for Stage IV NSCLC.
- Measurable disease as defined by the Response Evaluation Criteria in Solid Tumors (RECIST)
- Eastern Cooperative Oncology Group (ECOG) performance status 0-2
- Age \> 18 years old
- Adequate bone marrow, liver and renal function, defined as:
- Absolute neutrophil count (ANC) greater than or equal to 1500/ul
- Hemoglobin greater than or equal to 10 g/dl
- Platelet count greater than or equal to 100,000/ul
- Total bilirubin less than or equal to 1.5 x upper limit of normal (except in subjects with documented Gilbert's syndrome)
- AST/ALT less than or equal to 1.5 x upper limit of normal
- Serum creatinine less than or equal to 1.8 mg/dl
- Fully recovered from any previous surgery (at least 4 weeks since major surgery)
- Fully recovered from previous radiation therapy (at least 2 weeks)
- All subjects must agree to practice approved methods of birth control (if applicable). A negative pregnancy test must be documented during the screening period for women of childbearing potential.
- Written informed consent and authorization to use and disclose health information (HIPAA) must be signed by the subject.
- Subjects with symptomatic brain metastases should be adequately treated and controlled prior to the initiation of the study. Subjects with asymptomatic brain metastases will be allowed in the study without any prior therapy for brain metastases.
Exclusion
- Concurrent cancer chemotherapy, biologic therapy or radiotherapy
- Administration of any investigational agent within 28 days prior to administration of current therapy
- Untreated symptomatic brain metastases
- Greater than or equal to Grade 2 neuropathy
- Concurrent serious infection
- Concomitant severe or uncontrolled underlying medical disease unrelated to the tumor, which is likely to compromise subject safety and affect the outcome of the study.
- Treatment for a cancer other the NSCLC within 5 years prior to enrollment, with the exception of basal cell carcinoma or carcinoma in situ of the cervix
- Any evidence of history of hypersensitivity for the taxane class of chemotherapy drugs
- History of positive serology for HIV
- Psychiatric disorder that prevents subjects from providing informed consent or following protocol instructions
- Pregnant or lactating women
Key Trial Info
Start Date :
September 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2015
Estimated Enrollment :
28 Patients enrolled
Trial Details
Trial ID
NCT01438307
Start Date
September 1 2011
End Date
September 1 2015
Last Update
May 24 2017
Active Locations (2)
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1
University of Alabama at Birmingham
Birmingham, Alabama, United States, 35294
2
Georgia Cancer Center
Atlanta, Georgia, United States, 30060