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Eisai Oncology to Present New Research on Product Portfolio and Pipeline at ASCO Annual Meeting
Date:5/17/2012

Phase I Safety Study of Farletuzumab, Carboplatin and Pegylated Liposomal Doxorubicin (PLD) in Patients with Platinum-Sensitive Epithelial Ovarian Cancer (EOC)

Poster SessionFarletuzumab

(MORAb-003)

Abstract No: 3084

 

Phase I and Pharmacokinetic Study of Farletuzumab in Solid Tumors

Poster SessionAmatuximab

(MORAb-009)

Abstract No: 7030

 

Amatuximab, A Chimeric Monoclonal Antibody to Mesothelin, in Combination with Pemetrexed and Cisplatin in Patients with Unresectable Pleural Mesothelioma: Results of a Multicenter Phase II Clinical Trial

Poster DiscussionMORAb-004

Abstract No: 3016

 

A First-in-Human Phase I Study of MORAb-004 (M4), a Humanized Monoclonal Antibody Recognizing Endosialin (TEM-1), in Patients with Solid Tumors

Poster DiscussionThe information discussed in this release is about investigational agents that are not Food and Drug Administration (FDA)-approved and investigational uses for FDA-approved products.  It is not intended to convey conclusions of efficacy and safety. There is no guarantee that any of these agents will successfully complete clinical development or gain FDA approval.

HALAVEN® (eribulin mesylate) InjectionHalaven is indicated for the treatment of patients with metastatic breast cancer who have previously received at least two chemotherapeutic regimens for the treatment of metastatic disease. Prior therapy should have included an anthracycline and a taxane either in the adjuvant or metastatic setting.

Important Safety Information about HALAVEN®Decreased White Blood Cells (Neutropenia)

Your doctor should do a blood test to monitor your blood cells before you receive each dose of HALAVEN, and should monitor you more often if you develop lower white blood cells. If you develop severe neutropenia lasting long
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