{"id":3461,"date":"2012-10-15T22:20:27","date_gmt":"2012-10-15T22:20:27","guid":{"rendered":"http:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/idera-pharmaceuticals-announces-completion-of-patient-enrollment-in-phase-2-trial-of-imo-3100-in-patients-with-psoriasis\/"},"modified":"2012-10-15T22:20:27","modified_gmt":"2012-10-15T22:20:27","slug":"idera-pharmaceuticals-announces-completion-of-patient-enrollment-in-phase-2-trial-of-imo-3100-in-patients-with-psoriasis","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/psoriasis\/idera-pharmaceuticals-announces-completion-of-patient-enrollment-in-phase-2-trial-of-imo-3100-in-patients-with-psoriasis\/","title":{"rendered":"Idera Pharmaceuticals Announces Completion of Patient Enrollment in Phase 2 Trial of IMO-3100 in Patients with Psoriasis"},"content":{"rendered":"<p><p>    CAMBRIDGE, Mass.--(BUSINESS WIRE)--  <\/p>\n<p>    Idera Pharmaceuticals today announced that it had completed    patient enrollment in its randomized, double-blind,    placebo-controlled Phase 2 trial of IMO-3100 in patients with    moderate-to-severe plaque psoriasis. IMO-3100 is an antagonist    of specific Toll-like Receptors (TLRs) that the Company is    developing for the treatment of psoriasis and other autoimmune    diseases. Idera anticipates top-line data from this study will    be available by year-end 2012. TLRs are a class of proteins    that play a key role in both inflammation and immunity. Through    the inhibition of specific TLRs, Ideras candidates may    represent a novel approach for the treatment of psoriasis,    lupus and other autoimmune diseases.  <\/p>\n<p>    In this Phase 2 proof-of-concept study, we are evaluating    multiple endpoints to assess the clinical activity of IMO-3100,    including the impact on Psoriasis Area Severity Index (PASI),    mean focal psoriasis severity, and Physician Global Assessment    (PGA) scores, said Dr. Robert Arbeit, Vice President of    Clinical Development at Idera. In addition to the clinical    assessments, we are evaluating biopsies of psoriasis plaques    for treatment-related changes in epidermal thickness and immune    cell infiltrates consistent with the intended mechanism of    action.  <\/p>\n<p>    We have made significant progress in advancing our autoimmune    disease program, including the completion of enrollment in the    Phase 2 trial of IMO-3100 in patients with psoriasis. said Dr.    Sudhir Agrawal, Chief Executive Officer of Idera. In addition,    our investigational new drug (IND) application for IMO-8400, a    lead candidate for lupus, is now active. We expect our phase 2    study of IMO-3100 and planned clinical trials of IMO-8400 will    help us to establish the benefits of inhibiting Toll-like    Receptor-mediated pathways, which include controlling the    induction of multiple cytokines, such as TNF-, IL-12, IL-6,    and IL-17, as well as downstream signaling. We look forward to    reporting top-line data from the Phase 2 study of IMO-3100 in    psoriasis and initiating clinical development of IMO-8400    before the end of 2012.  <\/p>\n<p>    Idera also announced today that its Investigational New Drug    application for IMO-8400 with the US Food and Drug    Administration is now active. IMO-8400, an antagonist of TLRs    7, 8, and 9, is Ideras second lead candidate for use in    treating autoimmune diseases, with lupus selected as an initial    indication for clinical development. Idera anticipates    initiating a Phase 1 dose escalation trial during the fourth    quarter of 2012 to evaluate the safety and pharmacodynamics of    IMO-8400 in healthy subjects. Following successful completion    of the Phase 1 study, Idera expects to initiate a Phase 2    clinical trial of IMO-8400 in patients with lupus.  <\/p>\n<p>    Recent and Upcoming Autoimmune Disease Program    Milestones  <\/p>\n<p>    Fourth Quarter 2012:  <\/p>\n<p>    Year 2013:  <\/p>\n<p>    About TLRs and Idera's Pipeline  <\/p>\n<p>    Toll-like Receptors (TLRs) play a key role in inflammation and    immunity. Of the 10 human TLRs identified to date, Idera is    developing compounds targeted to TLRs 3, 7, 8, and 9, which are    expressed in different cells and serve unique functions. Using    its chemistry-based approach, Idera has created novel drug    candidates that modulate immune responses through either    activation or inhibition of specific TLRs. Inhibition of    specific TLRs may be useful in treating autoimmune disorders,    such as systemic lupus erythematosus (SLE), psoriasis, and    rheumatoid arthritis, by blocking the induction of multiple    cytokines and signaling pathways. Idera's lead clinical    candidates for application in autoimmune diseases are IMO-3100,    an antagonist of TLR7 and TLR9, and IMO-8400, an antagonist of    TLRs 7, 8, and 9.  <\/p>\n<\/p>\n<p>See the original post here:<br \/>\n<a target=\"_blank\" href=\"http:\/\/finance.yahoo.com\/news\/idera-pharmaceuticals-announces-completion-patient-120000179.html;_ylt=A2KJ3CcijHxQi1EAMVj_wgt.\" title=\"Idera Pharmaceuticals Announces Completion of Patient Enrollment in Phase 2 Trial of IMO-3100 in Patients with Psoriasis\">Idera Pharmaceuticals Announces Completion of Patient Enrollment in Phase 2 Trial of IMO-3100 in Patients with Psoriasis<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> CAMBRIDGE, Mass.--(BUSINESS WIRE)-- Idera Pharmaceuticals today announced that it had completed patient enrollment in its randomized, double-blind, placebo-controlled Phase 2 trial of IMO-3100 in patients with moderate-to-severe plaque psoriasis. IMO-3100 is an antagonist of specific Toll-like Receptors (TLRs) that the Company is developing for the treatment of psoriasis and other autoimmune diseases.  <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/psoriasis\/idera-pharmaceuticals-announces-completion-of-patient-enrollment-in-phase-2-trial-of-imo-3100-in-patients-with-psoriasis\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[22],"tags":[],"class_list":["post-3461","post","type-post","status-publish","format-standard","hentry","category-psoriasis"],"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/3461"}],"collection":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/comments?post=3461"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/3461\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=3461"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=3461"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=3461"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}