Idera Pharmaceuticals Expands Pipeline by Initiating Clinical Development of Proprietary TLR Antagonist Candidate IMO-9200
- IND application for Phase 1 clinical trial of IMO-9200 in healthy volunteers accepted by FDA; patient dosing on track to begin in fourth quarter
- New IMO-9200 data presented at 10th Annual Meeting of the Oligonucleotide Therapeutics Society demonstrate inhibition of TLR-mediated immune responses in multiple preclinical models
CAMBRIDGE, Mass., Oct. 14, 2014 -- Idera Pharmaceuticals, Inc. (IDRA), a clinical-stage biopharmaceutical company developing nucleic acid therapeutics for patients with cancer and rare diseases, today announced it has advanced IMO-9200 into Phase 1 clinical development following acceptance of an Investigational New Drug application by the U.S. Food and Drug Administration.
- Published: 14 October 2014
- Written by Editor