Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 12:30 AM
Ignite Modification Date: 2025-12-25 @ 12:30 AM
NCT ID: NCT01305967
Eligibility Criteria: Inclusion Criteria: * Age of 18-70 years * Patients with histologically or cytologically confirmed Non-Small Cell Lung Cancer * Patients who had failed more than 1 cycle of standard therapy with advanced or metasatic stage not available to any of resectable surgery or radiotherapy. * Patients with measurable lesions * Eatern Cooperative Oncolgy Group status 0 to 2. * Life expectancy \>/= 5 months * Patients with adequate organ(heart, kidney, liver)and bone marrow function, as defined by 1. Absolute neutrophil count \>/= 1.5 x 10\^9/L, Platelet count \>/= 100 x 10\^9/L 2. Total bilirubin \</= upper limit of normal 3. Aspartate Aminotransferase and/or Alanine Aminotransferase \</= 2 x upeer limit of normal 4. creatinine \</= 1.5 x upeer limit of normal * Patients who have signed the informed consent form. Exclusion Criteria: * Female volunteers admitted to the study must be using a reliable means of contraception * Received radiation therapy within 6 weeks before randomization * Known brain or spinal cord metastases * Have acute infection * Have active infection or serious concomitant systemic disorder incompatible with the study * Presence or history of malignancy other than Non-Small Cell Lung Cancer * Have severe neurologic or psychological disorder * Patients who have to receive other chemo-radiotherapy or immunotherapy * Patients who have received chemotherapy within the previous 30 days * Patients who are candidates for combined modality treatment. * Patients who have participated in a clinical study within the previous 30 days
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 70 Years
Study: NCT01305967
Study Brief:
Protocol Section: NCT01305967