Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT02152059

A Study to Evaluate the Good and Bad Effects of BIBF1120 in Small Cell Lung Cancer Patients Who Have Previously Benefited From First-line Platinum-based Chemotherapy

A Phase II Study of BIBF1120 in Recurrent and Platinum-Sensitive Small Cell Lung Cancer (SCLC)

Status
Withdrawn
Phase
Phase 2
Study type
Interventional
Enrollment
0 (actual)
Sponsor
AHS Cancer Control Alberta · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is being done to evaluate the good and bad effects of BIBF1120 in recurrent, platinum-sensitive small cell lung cancer patients and to see if BIBF1120 may or may not be more effective and better tolerated than standard therapy. The purpose of this study is to: * Find out the proportion of patients with their small small cell lung cancer controlled for at least 90 days after treatment with BIBF1120 * Compare the response rate, survival and side effects of BIBF1120 in recurrent, platinum-sensitive small cell lung cancer patients * Identify a group of patients who will benefit the most from BIBF1120 In this study, patients will receive BIBF1120 at 200 mg twice daily continuously. A cycle will be 21 days. During treatment, the dose of BIBF1120 will be held or reduced to lower doses if patients do not tolerate it well or if the doctors are concerned about the side effects of BIBF1120 on individual patients.

Detailed description

This study is being done to evaluate the effects of BIBF1120 in recurrent, platinum-sensitive small cell lung cancer patients. Primary Objectives: * To investigate the efficacy and safety of a novel VEGFR-2 and FGFR-1 targeting agent, BIBF1120, in previously treated, platinum-sensitive small cell lung cancer patients. Secondary Objectives: * To correlate response to the apoptotic biomarkers, Bcl-XL/Bcl-2 and FDGR-1 amplification. * To correlate response with baseline FLT-PET SUV uptake and change in FLT-PET SUV uptake. All eligible patients will be treated with 200 mg bid of BIBF1120 daily and 21 days will be considered as one cycle

Conditions

Interventions

TypeNameDescription
DRUGBIBF1120BIBF1120 is a VEGFR, FGFR and PDGFR inhibitor

Timeline

Start date
2014-07-01
Primary completion
2016-07-01
Completion
2016-07-01
First posted
2014-06-02
Last updated
2016-07-06

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT02152059. Inclusion in this directory is not an endorsement.