A Comparative Study Of PF-06439535 Plus Paclitaxel-Carboplatin And Bevacizumab Plus Paclitaxel-Carboplatin Patients With Advanced Non-Squamous NSCLC
This is a multinational, double-blind, randomized, parallel-group Phase 3 clinical trial evaluating the efficacy and safety of bevacizumab-Pfizer plus paclitaxel and carboplatin versus bevacizumab-EU plus paclitaxel and carboplatin in first-line treatment for patients with advanced (unresectable, locally advanced, recurrent or metastatic) non-squamous NSCLC.
Checked against the public recordLast updated Feb 7, 2019 · Source: ClinicalTrials.gov
What this study is about
- Purpose
- Treatment
- Study type
- Interventional
- Phase
- Phase 3
- Sponsor
- Pfizer
- Interventions being studied
- Drug: Bevacizumab-Pfizer; Drug: Bevacizumab-EU; Drug: Paclitaxel; Drug: Carboplatin
How this study is categorized
These labels come from structured fields and exact terms in the public record.
Who may be able to participate
Inclusion Criteria: * Male and female patients age at least 18 years of age, or age of consent in the region. * Newly diagnosed Stage IIIB or IV non-small cell lung cancer (according to Revised International System for Staging Lung Cancer criteria of 2010) or recurrent non-small cell lung cancer (NSCLC). * Histologically or cytologically confirmed diagnosis of predominately non-squamous NSCLC. * Be eligible to receive study treatment of bevacizumab, paclitaxel, and carboplatin based on local standard of care, for the treatment of advanced or metastatic non-squamous NSCLC. Exclusion Criteria: * Small cell lung cancer (SCLC) or combination SCLC and NSCLC. Squamous-cell tumors and mixed adenosquamous carcinomas of predominantly squamous nature. * Evidence of a tumor that compresses or invades major blood vessels or tumor cavitation that is likely to bleed. * Known sensitizing EGFR mutations (for example, deletion 19 or L858R) or EML4-ALK translocation positive mutations. * Prior systemic therapy for NSCLC; prior neoadjuvant or adjuvant therapy is allowed if surgical resection for primary disease was performed.
Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.
U.S. locations
- Southern Cancer Center, PCDaphne, Alabama
- Southern Cancer Center, PCMobile, Alabama
- Southern Cancer Center, PCMobile, Alabama
- Beaver Medical Group, L.P.Highland, California
- Cancer Center of Central ConnecticutNew Britain, Connecticut
- Cancer Center of Central ConnecticutSouthington, Connecticut
- Phoebe Putney Memorial HospitalAlbany, Georgia
- Swedish Covenant HospitalChicago, Illinois
- Meritus Center for Clinical ResearchHagerstown, Maryland
- Holy Cross Hospital Resource CenterSilver Spring, Maryland
- Maryland Oncology & Hematology, PASilver Spring, Maryland
- Holy Cross Hospital, Hospital PharmacySilver Spring, Maryland
Source and freshness
Processed from ClinicalTrials.gov. Last public update: Feb 7, 2019. Always confirm current availability with the study team.