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FDA clears Idera psoriasis therapy trial

Idera Pharmaceuticals has received notification from the Food and Drug Administration (FDA) to carry on with a Phase 2 clinical trial of IMO-3100 in patients with psoriasis.

IMO-3100 is a dual antagonist of Toll-like receptor (TLR) 7 and TLR9, which is indicated as a therapy for autoimmune and inflammatory diseases.

In July 2011, the company submitted a Phase 2 protocol to evaluate IMO-3100 in patients with psoriasis over a 12-week treatment period, which was put on clinical hold by the FDA.

In October 2011, the company submitted a new Phase 2 protocol to evaluate IMO-3100 in patients with psoriasis over a 4-week treatment period, which led to notification of FDA authorization to proceed.

Idera chairman and CEO Sudhir Agrawal said the company is geared up to conduct Phase 2 trial of dual-TLR antagonist to treat autoimmune diseases and are likely to initiate the study in the first half of 2012.