June 19, 2013 7:42 AM ET

Pharmaceuticals

Company Overview of Emergent Product Development Seattle, LLC

Company Overview

Emergent Product Development Seattle, LLC develops therapeutic products. It develops oncology and autoimmune protein therapeutic products, which include SBI-087 for the treatment of rheumatoid arthritis; SBI-087 for the treatment of systemic lupus erythematosus; TRU-016 for the treatment of B-cell malignancies; DRACO (Anti-CD3) SMIP therapeutic for the treatment of autoimmune and transplant diseases; X1 Anti-TNF-Based SCORPION therapeutics for the treatment of autoimmune diseases; and X2 CTLA-4-based SCORPION therapeutics for the treatment of autoimmune diseases. The company was formerly known as Trubion Pharmaceuticals, Inc. and changed its name to Emergent Product Development Seattle, LLC ...

Detailed Description

2401 4th Avenue

Suite 1050

Seattle, WA 98121

United States

Founded in 1999

73 Employees

Phone:

206-838-0500

Fax:

206-838-0503

Key Executives for Emergent Product Development Seattle, LLC

Emergent Product Development Seattle, LLC does not have any Key Executives recorded.

Emergent Product Development Seattle, LLC Key Developments

Emergent Product Development Seattle, LLC Receives Written Notification from Abbott Biotherapeutics Corp. to Terminate Collaboration and License Agreement

On December 21, 2011, Emergent BioSolutions Inc. and Emergent Product Development Seattle, LLC received written notification from Abbott Biotherapeutics Corp. of Abbott’s decision to terminate the collaboration and license agreement between the company and Abbott for the joint worldwide development and commercialization of TRU-016. Abbott informed the company that its decision was a result of its portfolio prioritization process. The termination will be effective on March 20, 2012, the ninetieth day after receipt of notice. TRU-016, Emergent’s humanized anti-CD37 mono-specific protein therapeutic, recently commenced a Phase 2 clinical study for chronic lymphocytic leukemia and is currently in Phase 1b clinical evaluation in non-Hodgkin’s lymphoma. These studies are expected to be completed, and final study data are expected to be available, in the first half of 2013. While the Agreement remains in effect, Abbott has an obligation to pay half of the collaboration project costs agreed to between the company and Abbott. Abbott also is obligated to pay the company milestone payments for milestone events achieved prior to March 20, 2012, including the $6 million milestone payment triggered by the company’s recent initiation of its Phase 2 clinical study of TRU-016 in CLL.

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