Study of Bavituximab Plus Paclitaxel and Carboplatin in Patients With Non-Small Cell Lung Cancer
Primary Purpose
Non-small Cell Lung Cancer
Status
Completed
Phase
Phase 2
Locations
India
Study Type
Interventional
Intervention
bavituximab plus paclitaxel and carboplatin
Sponsored by

About this trial
This is an interventional treatment trial for Non-small Cell Lung Cancer focused on measuring NSCLC
Eligibility Criteria
Key Inclusion Criteria:
- Adults over age 18 years of age with a life expectancy of at least 3 months
- Histologically or cytologically confirmed non-small cell lung cancer at stage IIIB (with pleural effusion), stage IV, or recurrence
- Measurable disease on cross sectional imaging at least 2 cm in longest diameter (1 cm if measured by spiral CT)
- Adequate hematologic (ANC ≥ 1500 cells/µL; Hemoglobin ≥9 g/dL; platelets ≥100,000/µL and ≤500,000/µL ), renal (serum creatinine ≤ 1.5 mg/dL or calculated creatinine clearance ≥ 60 mL/min), and hepatic function (bilirubin ≤ 1.5 x ULN, ALT ≤ 3 x ULN, AST ≤ 3 x ULN)
- D-dimer ≤ 2 x ULN
Key Exclusion Criteria:
- Small cell or mixed histology
- Known history of bleeding diathesis or coagulopathy
- Any current evidence of clinically significant bleeding defined as gross hematuria, hemoptysis, or GI bleeding
- Any history of thromboembolic events (e.g., deep vein thrombosis or pulmonary thromboembolism)
- Prior chemotherapy, immunotherapy or radiotherapy to an area of measurable disease unless disease had recurred after radiotherapy
- Radiotherapy within 2 weeks preceding Study Day 1
- Symptomatic or clinically active CNS disease or metastatic lesions
- Major surgery within 4 weeks of Study Day 1
- Uncontrolled intercurrent disease (e.g., diabetes, hypertension, thyroid disease)
- Any history of angina pectoris, coronary artery disease or cerebrovascular accident, or transient ischemic attack
- A history of any condition requiring anti-platelet therapy with the exception of general cardiovascular prophylaxis with aspirin. Anti-platelet agents are prohibited during the study.
- Requirement for chronic daily treatment with NSAIDs, anti-platelet drugs, or steroids
Sites / Locations
- Apollo Hospital
- Kidwai Hospital
- M S Ramaiah Hospital
- Bangalore Institute of Oncology Speciality Centre
- Nizam's Institute of Medical Sciences
- Yashoda Hospital
- RCC Medical College
- Orchid Nursing Home
- Ruby Hall Clinic
Outcomes
Primary Outcome Measures
Overall response (complete response + partial response) to a combination of bavituximab plus carboplatin and paclitaxel in patients with previously untreated locally advanced or metastatic non-small-cell lung cancer
Secondary Outcome Measures
Time to tumor progression, duration of response, overall survival and safety
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00687817
Brief Title
Study of Bavituximab Plus Paclitaxel and Carboplatin in Patients With Non-Small Cell Lung Cancer
Official Title
A Phase II Safety and Efficacy Study of Bavituximab Plus Paclitaxel and Carboplatin in Patients With Previously Untreated Locally Advanced or Metastatic Non-Small Cell Lung Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
March 2011
Overall Recruitment Status
Completed
Study Start Date
June 2008 (undefined)
Primary Completion Date
July 2010 (Actual)
Study Completion Date
July 2010 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Peregrine Pharmaceuticals
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The primary objective of this study is to determine the overall response rate (complete response + partial response) to a combination of bavituximab plus carboplatin and paclitaxel in patients with previously untreated locally advanced or metastatic non-small cell lung cancer.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-small Cell Lung Cancer
Keywords
NSCLC
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
49 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
bavituximab plus paclitaxel and carboplatin
Intervention Description
Weekly bavituximab dose of 3 mg/kg until disease progression, and up to 6 cycles of carboplatin at a dose of AUC=5 and paclitaxel 175 mg/m2 every 21 days (21-day cycles)
Primary Outcome Measure Information:
Title
Overall response (complete response + partial response) to a combination of bavituximab plus carboplatin and paclitaxel in patients with previously untreated locally advanced or metastatic non-small-cell lung cancer
Time Frame
one year
Secondary Outcome Measure Information:
Title
Time to tumor progression, duration of response, overall survival and safety
Time Frame
Approximately 1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Key Inclusion Criteria:
Adults over age 18 years of age with a life expectancy of at least 3 months
Histologically or cytologically confirmed non-small cell lung cancer at stage IIIB (with pleural effusion), stage IV, or recurrence
Measurable disease on cross sectional imaging at least 2 cm in longest diameter (1 cm if measured by spiral CT)
Adequate hematologic (ANC ≥ 1500 cells/µL; Hemoglobin ≥9 g/dL; platelets ≥100,000/µL and ≤500,000/µL ), renal (serum creatinine ≤ 1.5 mg/dL or calculated creatinine clearance ≥ 60 mL/min), and hepatic function (bilirubin ≤ 1.5 x ULN, ALT ≤ 3 x ULN, AST ≤ 3 x ULN)
D-dimer ≤ 2 x ULN
Key Exclusion Criteria:
Small cell or mixed histology
Known history of bleeding diathesis or coagulopathy
Any current evidence of clinically significant bleeding defined as gross hematuria, hemoptysis, or GI bleeding
Any history of thromboembolic events (e.g., deep vein thrombosis or pulmonary thromboembolism)
Prior chemotherapy, immunotherapy or radiotherapy to an area of measurable disease unless disease had recurred after radiotherapy
Radiotherapy within 2 weeks preceding Study Day 1
Symptomatic or clinically active CNS disease or metastatic lesions
Major surgery within 4 weeks of Study Day 1
Uncontrolled intercurrent disease (e.g., diabetes, hypertension, thyroid disease)
Any history of angina pectoris, coronary artery disease or cerebrovascular accident, or transient ischemic attack
A history of any condition requiring anti-platelet therapy with the exception of general cardiovascular prophylaxis with aspirin. Anti-platelet agents are prohibited during the study.
Requirement for chronic daily treatment with NSAIDs, anti-platelet drugs, or steroids
Facility Information:
Facility Name
Apollo Hospital
City
Bannerghatta Rd.
State/Province
Banglore
ZIP/Postal Code
560 076
Country
India
Facility Name
Kidwai Hospital
City
Munigowda Road
State/Province
Banglore
ZIP/Postal Code
560 027
Country
India
Facility Name
M S Ramaiah Hospital
City
New BEL Rd
State/Province
Banglore
ZIP/Postal Code
560 054
Country
India
Facility Name
Bangalore Institute of Oncology Speciality Centre
City
Sampangi Ram Nagar
State/Province
Banglore
ZIP/Postal Code
560 027
Country
India
Facility Name
Nizam's Institute of Medical Sciences
City
Panjagutta
State/Province
Hyderabad
ZIP/Postal Code
500 082
Country
India
Facility Name
Yashoda Hospital
City
Somajiguda
State/Province
Hyderabad
ZIP/Postal Code
500 082
Country
India
Facility Name
RCC Medical College
City
Trivandrum
State/Province
Kerala
ZIP/Postal Code
695 011
Country
India
Facility Name
Orchid Nursing Home
City
Phoolanbhaghan
State/Province
Kolkata
Country
India
Facility Name
Ruby Hall Clinic
City
Pune
ZIP/Postal Code
411-001
Country
India
12. IPD Sharing Statement
Citations:
PubMed Identifier
25236982
Citation
Digumarti R, Bapsy PP, Suresh AV, Bhattacharyya GS, Dasappa L, Shan JS, Gerber DE. Bavituximab plus paclitaxel and carboplatin for the treatment of advanced non-small-cell lung cancer. Lung Cancer. 2014 Nov;86(2):231-6. doi: 10.1016/j.lungcan.2014.08.010. Epub 2014 Aug 24.
Results Reference
derived
Learn more about this trial
Study of Bavituximab Plus Paclitaxel and Carboplatin in Patients With Non-Small Cell Lung Cancer
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