Clinical Trials for Mesothelioma Patients: Novartis LBH589 Study Description

Read the study description for a current clinical trial being conducted to study the effects of Novartis LBH589 for patients who have been diagnosed with mesothelioma. Please note: this information is provided by Weitz & Luxenberg for informational purposes only. For additional information, contact Novartis at 1-800-340-6843.

Study Description

Phase, Type and Design: Phase I Interventional Study; Treatment, Non-Randomized, Open Label, Active Control, Single Group Assignment, Safety/Efficacy Study

Primary Outcome Measure: Pharmacokinetic (PK) parameters Safety and tolerability (days 1-10) assessed by AEs, SAEs, labs, ECG reports, radiology reports.

Secondary Outcome Measure : Response rate assessed by comparing tumor size via radiology scans (CTs or MRIs) Safety and tolerability (until disease progression, unacceptable toxicity or study completion) assessed by duration of patient participation

Requisite Conditions: Carcinoma, Non-Small-Cell Lung Mesothelioma

Courtesy of ClinicalTrials.gov.

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