Study of Paclitaxel/Carboplatin With or Without Bavituximab in Previously Untreated Non Small-Cell Lung Cancer

• Status: Completed
• Trial end date: 2013-09-01
• Target enrollment: 0
• Participant gender: All

Summary

This is a randomized, open-label, multicenter, phase 2 study comparing Paclitaxel/Carboplatin with or without bavituximab in patients that have previously untreated locally advanced or metastatic non-small cell lung cancer (NSCLC).

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Peregrine Pharmaceuticals
• Treatments: Albumin-Bound Paclitaxel; Antibodies, Monoclonal; Bavituximab; Carboplatin; Paclitaxel

Criteria

Key Inclusion Criteria:

• Adults over 18 years of age with a life expectancy of at least 3 months.

• Histologically or cytologically confirmed stage IIIB or stage IV non-squamous NSCLC that has not been previously treated with systemic chemotherapy.

• Measurable disease by Response Evaluation Criteria in Solid Tumors (RECIST, Version 1.1).

• Adequate hematologic, renal and hepatic function.

• PT / INR ≤ 1.5 × ULN, aPTT ≤ 1.5 × ULN and D-dimer ≤ 3 × ULN.

Key Exclusion Criteria:

• Squamous cell, small cell, or mixed histology.

• Known history of bleeding diathesis or coagulopathy.

• Cavitary tumors or tumors abutting large blood vessels.

• Bleeding: Clinically significant bleeding, such as gross hematuria, GI bleeding and hemoptysis, within 12 months of Screening.

• Venous thromboembolic events (e.g., deep vein thrombosis or pulmonary thromboembolism) within 6 months of Screening.

• Ongoing therapy with oral or parenteral anticoagulants.

• Concurrent estrogens, anti-estrogens or progesterone compounds.

• Grade 2 or higher peripheral neuropathy.

• Radiotherapy within 2 weeks preceding Study Day 1.

• Symptomatic or clinically active brain metastases.

• Major surgery within 4 weeks of Study Day 1.

• Uncontrolled intercurrent disease (e.g., diabetes, hypertension, thyroid disease).

• Symptomatic coronary artery disease, cerebrovascular accident,transient ischemic attack, myocardial infarction, or unstable angina pectoris within 6 months of Screening.