Lipid Therapeutics announces positive topline Phase IIb results with LT-02 in patients with ulcerative colitis
The Phase IIb trial met the primary end point, change in SCCAI (Simple Clinical Colitis Activity Index), for patients refractory to standard first-line intervention who were treated with LT-02 at 0.8g four times a day (51% reduction with LT-02 vs 33% reduction with placebo; p <0.05). Patients who received one of two lower doses of LT-02 also showed a positive benefit. The excellent safety profile of LT-02 treatment was comparable to placebo at all three doses.
The Phase IIb trial was a randomized, multi-center, double-blind, parallel group, placebo-controlled, dose ranging study that was designed to investigate the efficacy and safety of LT-02 in patients with mesalazine-refractory ulcerative colitis. 156 patients were enrolled into the trial at 24 centers in Germany, Lithuania and Romania. Patients were randomized to receive one of three doses of LT-02 or placebo and were treated for a period of 12 weeks. Lipid Therapeutics intends to present full data on the trial at UEGW in Stockholm in October 2011.
Dr. Gerhard Keilhauer, CEO of Lipid Therapeutics, said: “The results that we have announced today are a key milestone for Lipid Therapeutics. We are delighted that LT-02, which has a novel mode of action, has been shown to be of significant benefit to patients with ulcerative colitis whose condition has not responded to the current mainstay of therapy, i.e. mesalazine. We will now discuss with our European partner, Dr. Falk Pharma, and with potential partners in the US and Japan how we can rapidly move this innovative therapeutic into a pivotal Phase III study, the next key step in making it available to ulcerative colitis patients as quickly as possible.”
Max Karner MD, University Clinic Heidelberg, Germany, who was the Principal Investigator for the study, said: “The positive clinical results that we have seen with patients treated with LT-02 clearly suggests that it has the potential to become a very attractive new treatment option for patients with ulcerative colitis who currently have limited options. I would like to take this opportunity to thank all of the investigators and patients who took part in this very important study which was completed ahead of schedule and has delivered excellent results.”
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