Skip to main content
OpenTrials
Completed

NCT Number: NCT01225302

A Study of Linifanib (ABT-869) in Combination With Carboplatin/Paclitaxel in Japanese Subjects With Non-Small Cell Lung Cancer (NSCLC)

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.

Completed

Looking for future studies?

Notify Me

Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • The subject must be 20 and older years of age.
  • The subject must have cytologically or histologically confirmed non-squamous NSCLC. Subjects may have a mixed histology but must be predominantly non-squamous to be eligible.
  • The subject must have advanced or metastatic (Stage IV [According to American Joint Committee on Cancer (AJCC) staging manual, 7th edition]) disease that is not amenable to surgical resection or radiation with curative intent.
  • The subject must have not received prior chemotherapy for NSCLC.
  • The subject has measurable disease, defined as at least 1 unidimensionally measurable lesion on a CT scan as defined by Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1.
  • The subject has an Easter Cooperative Oncology Group (ECOG) Performance Score of 0-1.
  • The subject must have adequate bone marrow, renal and hepatic function.

Exclusion criteria

  • The subject has hypersensitivity to paclitaxel or to other drugs formulated with polyethoxylated castor oil (Cremophor).
  • The subject has received any anti-cancer therapy for treatment of NSCLC including investigational agents, immunotherapy, traditional Chinese medicine/herbal remedies, hormonal, "targeted" agents (i.e., erlotinib, imatinib), biologic therapy or cytotoxic chemotherapy (i.e., alkylating agents, microtubule inhibitors, antimetabolites).
  • The subject has a history of another active cancer within the past 5 years except cervical cancer in situ, in situ carcinoma of the bladder, squamous cell or basal cell carcinoma of the skin.
  • The subject has active ulcerative colitis, Crohn's disease, celiac disease or any other conditions that interfere with absorption.
  • The subject has a medical condition, which in the opinion of the study investigator places them at an unacceptably high risk for toxicities.
  • The subject is pregnant or breast feeding.
  • The subject has NSCLC with a predominant squamous cell histology.

Treatment and study plan

Linifanib

Drug

Low dose linifanib (once a day)

Other names: ABT-869

carboplatin

Drug

Given on Day 1 of every 21-day cycle

Other names: Paraplatin

paclitaxel

Drug

Given on Day 1 of every 21-day cycle

Other names: Taxol

Primary outcomes

  1. Safety (Number of patients with adverse events and/or dose-limiting toxicities)

    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.

Secondary outcomes

  1. Preliminary tumor response

    Time frame: Week 6

    Computed Tomography (CT) scan

  2. Preliminary tumor response

    Time frame: Week 12

    Computed Tomography (CT) scan

  3. Preliminary tumor response

    Time frame: Week 18

    Computed Tomography (CT) scan

  4. Preliminary tumor response

    Time frame: Week 24

    Computed Tomography (CT) scan

  5. Preliminary tumor response

    Time frame: Week 30

    Computed Tomography (CT) scan

  6. Preliminary tumor response

    Time frame: Week 36

    Computed Tomography (CT) scan

  7. Preliminary tumor response

    Time frame: Week 42

    Computed Tomography (CT) scan

  8. Preliminary tumor response

    Time frame: Week 48

    Computed Tomography (CT) scan

  9. Preliminary tumor response

    Time frame: Week 54

    Computed Tomography (CT) scan

Sponsors and collaborators

Lead sponsor

AbbVie

Industry

Registry information

Official study title

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

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
Oct 21, 2010
Registry last updated
Nov 21, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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.

Published trials that share one or more normalized conditions with this study.