Pipeline :: Autoimmunity / Inflammation

Dynavax has pioneered a new approach to treating autoimmune and inflammatory diseases with its oligonucleotide-based Toll-like Receptor (TLR) inhibitors, called immunoregulatory sequences (IRS). TLRs are key receptors of the innate immune system that can induce strong inflammatory responses.

In February 2010, Dynavax announced the selection of a candidate for clinical development in its endosomal Toll-like Receptor (TLR) inhibitor collaboration with GlaxoSmithKline. The selected molecule DV1179, a bifunctional TLR inhibitor, has moved into advanced preclinical IND-enabling studies that could allow clinical development to begin as early as this year.

In late 2008, Dynavax and GlaxoSmithKline entered into a worldwide strategic allianceto discover, develop, and commercialize novel TLR inhibitors for diseases such as lupus, psoriasis, and rheumatoid arthritis. We are conducting research and early clinical development in up to four programs and are eligible to receive future potential development and commercialization milestones totaling approximately $200 million per program. GSK can exercise its exclusive option to license each program upon achievement of proof-of-concept or earlier upon certain circumstances. After exercising its option, GSK will carry out further development and commercialization of these products. We will receive tiered, up to double-digit royalties on sales and have retained an option to co-develop and co-promote one product.

Commercial Opportunity

Over 20 million individuals in the U.S. and Europe have autoimmune diseases such as lupus, psoriasis, and rheumatoid arthritis. Key biologic drugs used to treat these conditions generate over $15 billion in worldwide sales each year.

Our TLR inhibitors have demonstrated a highly targeted effect on key immune cells and pathways that play a role in multiple autoimmune and inflammatory diseases. In contrast, currently marketed and pipeline products are broadly immunosuppressive with variable efficacy and substantial toxicity.