A Single-Center, Randomized, Double-Blind, Active, and Placebo-Controlled Study of KAI-1678, a Novel PKC-Epsilon Inhibitor, in the Treatment of Acute Postoperative Orthopedic Pain

被引:20
作者
Moodie, John E. [1 ]
Bisley, Eileen J. [1 ]
Huang, Saling [2 ]
Pickthorn, Karen [2 ]
Bell, Gregory [2 ,3 ]
机构
[1] Waikato Clin Res 2008 Ltd, Hamilton 3248, New Zealand
[2] KAI Pharmaceut Inc, San Francisco, CA USA
[3] Univ Calif San Francisco, San Francisco, CA 94143 USA
关键词
KAI-1678; Acute Pain; Analgesic; Epsilon Protein Kinase C Inhibitor; Postoperative Orthopedic Pain; PROTEIN-KINASE-C; PERIPHERAL NEUROPATHY; BALANCED ANALGESIA; SENSORY NEURONS; BRADYKININ; RAT; SENSITIZATION; FIBERS; MICE;
D O I
10.1111/pme.12088
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
Objective KAI-1678, a novel inhibitor of the interaction of the epsilon isoform of protein kinase C (epsilon PKC) with its intracellular receptor, has demonstrated activity in countering hyperalgesia in several models of pain. In this controlled randomized trial, KAI-1678 was tested for analgesic activity in an orthopedic acute postoperative pain setting. Design Following hip or knee replacement surgery, subjects were treated with KAI-1678, ketorolac, or saline. Subjects recorded their pain intensity on a visual analog scale and rated their quality of analgesia. The pain intensity differences between baseline and the evaluations were summed over the first 4 hours. Results The analysis revealed that, while ketorolac displayed good analgesic activity, KAI-1678 was not significantly different than placebo. Analgesia quality ratings similarly did not show a difference between KAI-1678 and placebo in this pain model. A small excess of infusion site erythema was seen with KAI-1678, but otherwise the drug was safe and well tolerated. Conclusions We investigated the safety and efficacy of a novel inhibitor of epsilon PKC and provide clinical evidence that inhibition of epsilon PKC with KAI-1678 is not effective in the treatment of acute postoperative orthopedic pain.
引用
收藏
页码:916 / 924
页数:9
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