Channel Therapeutics Corporation announced that it achieved its endpoints in two pre-clinical in vivo models of the Company’s nerve block formulations for acute pain, showing material improvement over the existing standard of care, bupivacaine, in both efficacy and duration. “We are very pleased with the results, which potentially demonstrate that nerve blocks with our NaV1.7 inhibitors may be viable options for the treatment of acute and postoperative pain,” stated Dr. Eric Lang, Chief Medical Officer of Channel. “Additionally, we believe this drug has the potential to improve on existing postoperative therapeutic options while opening the door for success with our other programs,” concluded Dr. Lang.
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