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: 2025-12-24 @ 7:04 PM
Ignite Modification Date: 2025-12-24 @ 7:04 PM
NCT ID: NCT02810457
Eligibility Criteria: Inclusion Criteria: * Patients aged 18 years or older * Newly diagnosed advanced (stage IV) /recurrent non-squamous NSCLC for which they had not received any systemic anti-cancer therapy for metastatic disease * Histologically or cytologically confirmed diagnosis of predominantly non-squamous NSCLC * Existence of at least 1 measurable lesion by RECIST v1.1 * Adequate hematological, renal and liver function * Eastern Collaborative Oncology Group Performance Status (ECOG PS) 0 or 1 * Life expectancy longer than 6 months Exclusion Criteria: * Small cell lung cancer (SCLC) or combination SCLC and NSCLC. Squamous-cell tumors and mixed adenosquamous carcinomas of predominantly squamous nature * Any unresolved toxicities from prior systemic therapy * Known sensitizing epidermal growth factor receptor (EGFR) mutations or echinoderm microtubule-associated protein-like 4-anaplastic lymphoma kinase (EML4-ALK) translocation positive mutations * Previous dosing with vascular endothelial growth factor (VEGF) inhibitor * Known hypersensitivity to any excipients of the Investigational Products (IPs) and combination chemotherapy * Use of prohibited concomitant medication * Known Hepatitis B, Hepatitis C, or human immunodeficiency virus (HIV) infection * Fertile men or women of childbearing potential not using adequate contraception. Other inclusion/exclusion criteria may apply.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT02810457
Study Brief:
Protocol Section: NCT02810457