MedPath

Phase 1/2 study of combination chemotherapy with Carboplatin, nab-Paclitaxel, and Bevacizumab for advanced non-squamous non-small cell lung cancer

Phase 1
Conditions
on-squamous Non-small-cell Lung Cancer
Registration Number
JPRN-UMIN000016735
Lead Sponsor
Hiroshima Asa City Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
35
Inclusion Criteria

Not provided

Exclusion Criteria

1) Squamous cell lung cancer 2) History of Severe drug allergies. 3) Double malignancies within 5 years 4) Uncontrolled ascites, pleural effusion or cardiac effusion 5) Current history of hemoptysis 6-7) High risk of bleeding or thrombus events 8) Evidence of bleeding diathesis or coagulopathy 9) Current or previous history of Pericardial effusion 10) Superior vena cava syndrome 11) Spinal cord compression 12) Current or previous (within the last 1 year) history of cerebrovascular disease 13) Traumatic fracture of unrecovery 14) History of active infection 15) Scheduled operation 16) Antithrombotic agent 17) Uncontrollable Gastrointestinal ulceration 18) Current or previous (within the last 1 year)history of GI perforation 19) Uncontrollable hypertension 20) Severe cardiac disease 21) Interstitial pneumonia or pulmonary fibrosis detectable on X ray 22) With grade2 or more neuropathy 23) Treatment history of bevacizumab 24) Pregnancy, breastfeeding or suspected of being pregnant 25) HBs positive patient 26) Others judged by attending physician

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
PhaseI Recommended Dose PhaseII Response Rate
Secondary Outcome Measures
NameTimeMethod
DCR, PFS, OS, Safety
© Copyright 2025. All Rights Reserved by MedPath