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:
2025-12-24 @ 2:25 PM
Ignite Modification Date:
2025-12-24 @ 2:25 PM
NCT ID:
NCT01047059
Eligibility Criteria:
Inclusion Criteria:
* Patients with histologically or cytologically proven non-squamos NSCLC stage IIIB with pleural effusion or stage IV
* ≥ 18 years of age
* Performance status ECOG 0-2
* Estimated life expectancy of at least 12 weeks
* Subjects with at least one measurable or nonmeasurable (CT or MRI) lesion according to RECIST
* Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements to be conducted within 7 days prior to screening:
* Hemoglobin ≥ 9.0 g/dL
* Absolute neutrophil count (ANC) ≥ 1,500 /mm3
* Platelet count ≥ 100 000/μL
* Total bilirubin ≤ 2 x ULN
* ALT, AST and alkaline phosphatase (AP) ≤ 2,5 x ULN
* PT-INR/PTT \< 1.5 x ULN
* Creatinine clearance (CrCl) ≥ 60 ml/min calculated by either Cockcroft-Gault or by 24 hours urine collection
* Written informed consent (after adequate explanation of the trial) to participate in the trial and to adhere to trial procedures, as well as consenting to data protection procedures
* No clinical or radiological sign of interstitial lung disease, no interstitial lung disease in the past
* Patients must be able to take oral medication
* In case of female patients with childbearing potential:
* negative serum or urine HCG in women with childbearing potential
* effective method of contraception (Pearl-Index not greater than 1%)
* at least 12 months after last menstruation
Exclusion Criteria:
* Patient has received prior chemotherapeutic regimens for advanced disease. Prior chemotherapy given as neoadjuvant or adjuvant therapy for early stage disease, completed at least 12 months prior to diagnosis of advanced stage disease, will not be considered as exclusion criterion.
* Patient has received prior EGFR-targeted therapy
* Squamous-cell carcinoma (SCC) histology, SCLC histology or mixed histology
* Evidence of tumor invading or abutting major blood vessels
* Patient has signs or symptoms of acute infection requiring systemic therapy (acute or within the last 14 days)
* Uncontrolled diabetes mellitus with HbA1c \> 7,5% or elevated blood glucose levels levels of \> 200 mg/dL
* History of uncontrolled heart disease (congestive heart failure \> NYHA class 2; active Coronary Arterial Disease (CAD), (MI more than 6 months prior to study entry is allowed); cardiac arrythmias requiring anti-arrythmic therapy (except, when controlled by beta blockers or digoxin) and/or uncontrolled hypertension (\> 150/100 mmHg)
* Impairment of gastrointestinal function or gastrointestinal disease that may significantly alter the absorption of erlotinib and (e.g. ulcerative disease, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome or small bowel resection, total parenteral nutrition with lipids)
* History of HIV infection or previously sero-positive for the virus
* History of Hepatitis B or/and C or previously sero-positive for the Hepatitis B or/and C virus
* Patients with seizure disorder requiring CYP3A4-inducing anti-epileptics
* History of organ allograft
* Patients with evidence or history of bleeding diathesis
* History of thrombotic disorders within the last 6 months prior to enrolment
* Fine needle biopsy or open biopsy within 1 week prior inclusion
* Clinically symptomatic leptomeningeal or brain metastases (patients with clinically stable brain metastases may be enrolled)
* Impaired wound healing, non-healing wounds, ulcers, fractures or any condition that provokes uncontrolled bleeding
* Preexisting neuropathia ≥ grade 2 • History of grade ≥2 hemoptysis (bright red blood of at least 2.5 ml)
* Patients undergoing renal dialysis
* Past or current history of cancer other than the entry diagnosis EXCEPT cervical carcinoma in situ, treated basal cell carcinoma, superficial bladder tumors \[Ta, Tis \& T1\] or any cancer curatively treated \> 3 years prior to study entry.
* Any person being in an institution on assignment of the respective authority
* Urine protein qualitative value of \> 30 in urinalysis or \> +1 in proteinuria testing by dipstick
* Any medical, mental or psychological condition which in the opinion of the investigator would not permit the patient to complete the study or understand the patient information
* Concomitant or intented anticoagulation therapy
* Planned surgical or dental invasive intervention (e.g. tooth extraction, planned surgeries) during the course of the study
* Any serious medical condition with organ impairment
* Hypersensitivity to bevacizumab or erlotinib or any of their ingredients
* Major surgery or significant traumatic injury within the last 4 weeks before inclusion
* Parallel participation in another clinical trial or participation in another clinical trial within the last 30 days or 7 half-life's, whatever is of longer duration, prior study start
* Pregnancy, breast feeding
* Claustrophobia
* Known allergic reaction to Gadolinium
* Heart pacemaker
* Ferromagnetic and electronic implants in special locations (e. g. cerebral)
* Cochlea implants
* known allergic reaction to non-ionic iodinated computed tomography contrast agents
* known hyperthyroidism
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
99 Years
Study:
NCT01047059
Study Brief:
Protocol Section:
NCT01047059