Linifanib
DrugLow dose linifanib (once a day)
Other names: ABT-869
NCT Number: NCT01225302
The primary objective of this study is to assess the safety and pharmacokinetics of linifanib, and identify tolerable dose of linifanib (ABT-869) in combination with carboplatin and paclitaxel in Japanese subjects with advanced or metastatic non-small cell lung cancer (NSCLC). Secondary objective is to obtain a preliminary efficacy of anti-tumor activity in the subjects as first-line treatment.
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Notify Me20 year–99 year
All sexes
Interventional
Phase 1
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Low dose linifanib (once a day)
Other names: ABT-869
Given on Day 1 of every 21-day cycle
Other names: Paraplatin
Given on Day 1 of every 21-day cycle
Other names: Taxol
Time frame: At each treatment visit (weekly for 6 weeks, then every 3 weeks)
Evaluation of vital signs, physical exams, clinical lab testing and adverse event monitoring.
Time frame: Week 6
Computed Tomography (CT) scan
Time frame: Week 12
Computed Tomography (CT) scan
Time frame: Week 18
Computed Tomography (CT) scan
Time frame: Week 24
Computed Tomography (CT) scan
Time frame: Week 30
Computed Tomography (CT) scan
Time frame: Week 36
Computed Tomography (CT) scan
Time frame: Week 42
Computed Tomography (CT) scan
Time frame: Week 48
Computed Tomography (CT) scan
Time frame: Week 54
Computed Tomography (CT) scan
AbbVie
Industry
A Phase 1 Study of Linifanib (ABT-869) in Combination With Carboplatin/Paclitaxel in Japanese Subjects With Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) as First-Line Treatment
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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