CTRI/2010/091/001348
Active, not recruiting
Phase 2
PHASE II CLINICAL TRIAL OF IMMUNOTHERAPY WITH AN ALLOGENEIC B7.1/HLA-A1 TRANSFECTED TUMOR CELL VACCINE (PT 107) IN PATIENTS WITH STAGES IIIB/IV NON-SMALL CELL LUNG CANCER THAT HAVE COMPLETED FIRST LINE CHEMOTHERAPY
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Health Condition 1: null- Advanced non-small cell lung cancer (Stages IIIB/IV) who have failed first line of chemotherapy
- Sponsor
- PIQUE THERAPEUTICS INC
- Enrollment
- 100
- Status
- Active, not recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Patients with documented stage IIIB or IV advanced or metastatic NSCLC who have completed 4\-6 cycles of platinum based chemotherapy, with or without radiation, and have either stable disease or have experienced disease progression (additional prior adjuvant chemotherapy is permitted).
- •2\. ECOG performance status 0\-2\.
- •3\. Presence of at least one measurable lesion according to RECIST criteria.
- •4\. Renal Requirements: The calculated creatinine clearance must be at least 50 ml/min.
- •5\. Pulmonary Function Requirements
- •All patients will undergo evaluation of pulmonary function prior to enrollment. Patients should have a FeV1 more than 30% of the predicted value and/or DLCO more than 30% of the predicted value with a PCO2 \< 45mm. Any patient enrolled in the protocol whose respiratory symptoms have experienced marked deterioration not related to a known cause (e.g. pneumonia, CHF or PE) will have request PFT evaluation and if the above parameters are not fulfilled will be excluded from the protocol.
- •6\. Age \> or \= 18 years.
- •7\. Signed informed consent.
- •8\. ANC \> or \=1000/mm3; PLT\> or \= 80,000/mm3\.
- •9\. Hemoglobin \> or \= 10 g/dL.
Exclusion Criteria
- •1\. Small cell carcinoma of the lung.
- •2\. Existing autoimmune disorders such as rheumatoid arthritis, systemic lupus erythematosus, Sjogren's disease etc; colitis, inflammatory bowel disease or pancreatitis within 10 years of study.
- •3\. Other active malignancies present within the past three years, except for basal and / or squamous cell carcinoma(s) or in situ cervical cancer.
- •4\. Concomitant steroid or other immunosuppressive therapy.
- •5\. Active infection, or less than 7 days since therapy for acute infections.
- •6\. Pericardial effusion.
- •7\. Currently receiving chemotherapy for another condition (such as arthritis).
- •8\. Active or symptomatic cardiac disease such as congestive heart failure, angina pectoris or recent myocardial infarction.
- •9\. Pregnant or lactating women (negative test for pregnancy required of women of child bearing potential).
- •10\. Refusal in fertile men or women to use effective birth control measures during and for six months after the completion of treatment on study.
Outcomes
Primary Outcomes
Not specified
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