A Study of Avastin (Bevacizumab) in Combination With Platinum-Containing Chemotherapy in Patients With Advanced or Recurrent Non-Squamous Cell Lung Cancer.
NCT00451906 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 2252
Last updated 2016-05-24
Summary
This single arm study will assess the safety and efficacy of Avastin combined with platinum-containing chemotherapy regimens in patients with advanced or recurrent non-squamous non-small cell lung cancer (NSCLC). Avastin will be given as first-line treatment in combination with platinum-based chemotherapy or in combination with any standard of care NSCLC first-line chemotherapy used in line with the licensed national prescribing information. Eligible patients will receive Avastin (15mg/kg iv on day 1 of each 3 week cycle) concomitantly with chemotherapy. Avastin treatment will continue after completion of chemotherapy cycles until disease progression, and the target sample size is 500+ individuals.
Conditions
- Non-Squamous Non-Small Cell Lung Cancer
Interventions
- DRUG
-
Platinum-based chemotherapy
As prescribed
- DRUG
-
Bevacizumab [Avastin]
15 mg/kg IV on Day 1 of each 3 week cycle
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Clinical Trials · Hoffmann-La Roche
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2006-08-31
- Primary Completion
- 2009-06-30
- Completion
- 2009-06-30
Countries
- Argentina
- Australia
- Austria
- Bosnia and Herzegovina
- Brazil
- Canada
- China
- Colombia
- Czechia
- Denmark
- Ecuador
- Egypt
- Estonia
- Finland
- France
- Germany
- Hong Kong
- Hungary
- Iceland
- Israel
- Italy
- Latvia
- Lebanon
- Lithuania
- Mexico
- Netherlands
- Poland
- Portugal
- Romania
- Russia
- Serbia
- Slovakia
- Slovenia
- Spain
- Sweden
- Switzerland
- Taiwan
- Turkey (Türkiye)
- United Kingdom
- Venezuela
Study Locations
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