Expired Study
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Hershey, Pennsylvania 17033


Purpose:

The primary objective of the study is to establish the phase II recommended dose of Vorinostat when administered in combination with the regimen of carboplatin, paclitaxel and bevacizumab for patients with previously untreated advanced non-small cell lunc cancer.


Study summary:

Since the regimen of bevacizumab, carboplatin and paclitaxel has become a standard regimen for the treatment of advanced non-squamous NSCLC, new studies in this patient population will have to include this as a reference arm. Addition of a fourth anti-cancer agent has now become the new strategy to improve the outcome for advanced non-squamous NSCLC. Since the regimen of Vorinostat, Carboplatin and Paclitaxel is already in advanced stage of development it is important to study the safety and tolerability of Vorinostat in combination with the three-drug regimen of Bevacizumab, Carboplatin and Paclitaxel. Therefore, we will evaluate Vorinostat when administered in combination with the regimen of Carboplatin, Paclitaxel and Bevacizumab for patients with previously untreated advanced non-small cell lung cancer.


Criteria:

Inclusion Criteria: - Advanced non-squamous NSCLC - No prior chemotherapy for advanced disease - ECOG performance status 0 or 1 - Measurable disease - Life expectancy > 3 months - Normal bone marrow, renal and hepatic function - Ability to take oral medications - Willingness to sign informed consent Exclusion Criteria: - History of brain metastasis - Evidence of thromboembolic phenomenon and treatment with anticoagulants - Pregnancy - Uncontrolled inter-current illness - Prior therapy with Paclitaxel


NCT ID:

NCT00702572


Primary Contact:

Principal Investigator
Chandra P Belani, MD
Penn State College of Medicine


Backup Contact:

N/A


Location Contact:

Hershey, Pennsylvania 17033
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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