A Randomized, Placebo-controlled Trial of the Analgesic Efficacy and Safety of the p38 MAP Kinase Inhibitor, Losmapimod, in Patients With Neuropathic Pain From Lumbosacral Radiculopathy

OBJECTIVES:Preclinical studies have demonstrated involvement of p38 mitogen-activated protein kinase signaling pathways in the development of persistent pain after peripheral nerve injury. A double-blind, randomized, placebo-controlled study was undertaken to evaluate the analgesic efficacy of losma...

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Veröffentlicht in:The Clinical journal of pain 2015-04, Vol.31 (4), p.283-293
Hauptverfasser: Ostenfeld, Thor, Krishen, Alok, Lai, Robert Y, Bullman, Jonathan, Green, Joanne, Anand, Praveen, Scholz, Joachim, Kelly, Madeline
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container_end_page 293
container_issue 4
container_start_page 283
container_title The Clinical journal of pain
container_volume 31
creator Ostenfeld, Thor
Krishen, Alok
Lai, Robert Y
Bullman, Jonathan
Green, Joanne
Anand, Praveen
Scholz, Joachim
Kelly, Madeline
description OBJECTIVES:Preclinical studies have demonstrated involvement of p38 mitogen-activated protein kinase signaling pathways in the development of persistent pain after peripheral nerve injury. A double-blind, randomized, placebo-controlled study was undertaken to evaluate the analgesic efficacy of losmapimod (GW856553), a novel p38α/β inhibitor, in patients with chronic neuropathic pain due to lumbosacral radiculopathy. MATERIALS AND METHODS:A total of 144 patients with at least moderate baseline pain intensity (average daily score of ≥4 on an 11-point pain intensity numeric rating scale) were randomized to receive losmapimod, 7.5 mg bid orally or placebo. All patients underwent a blinded placebo run-in period for 7 days before receiving losmapimod/placebo for 28 days. Efficacy and safety evaluations were undertaken weekly. RESULTS:The adjusted mean treatment difference for the change from baseline to week 4 in numeric rating scale was −0.36 U (95% confidence interval, −0.84, 0.13; P=0.149) in favor of losmapimod over placebo; this was not considered clinically meaningful. Statistically significant differences in favor of losmapimod were observed, however, for several secondary endpoints of emotional, physical, and social functioningOswestry Disability Index; Profile of Mood States total score; Short-Form 36 Health Survey physical functioning, bodily pain, general health, role emotional, social functioning, and vitality domains; and Short-Form 36 physical, and mental components. There were no unexpected findings related to safety or tolerability following treatment with losmapimod. DISCUSSION:Losmapimod could not be differentiated from placebo in terms of analgesia. The lack of response could reflect insufficient losmapimod levels in the spinal cord or differences between lumbosacral radiculopathy and animal models of neuropathic pain.
doi_str_mv 10.1097/AJP.0000000000000122
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A double-blind, randomized, placebo-controlled study was undertaken to evaluate the analgesic efficacy of losmapimod (GW856553), a novel p38α/β inhibitor, in patients with chronic neuropathic pain due to lumbosacral radiculopathy. MATERIALS AND METHODS:A total of 144 patients with at least moderate baseline pain intensity (average daily score of ≥4 on an 11-point pain intensity numeric rating scale) were randomized to receive losmapimod, 7.5 mg bid orally or placebo. All patients underwent a blinded placebo run-in period for 7 days before receiving losmapimod/placebo for 28 days. Efficacy and safety evaluations were undertaken weekly. RESULTS:The adjusted mean treatment difference for the change from baseline to week 4 in numeric rating scale was −0.36 U (95% confidence interval, −0.84, 0.13; P=0.149) in favor of losmapimod over placebo; this was not considered clinically meaningful. Statistically significant differences in favor of losmapimod were observed, however, for several secondary endpoints of emotional, physical, and social functioningOswestry Disability Index; Profile of Mood States total score; Short-Form 36 Health Survey physical functioning, bodily pain, general health, role emotional, social functioning, and vitality domains; and Short-Form 36 physical, and mental components. There were no unexpected findings related to safety or tolerability following treatment with losmapimod. DISCUSSION:Losmapimod could not be differentiated from placebo in terms of analgesia. 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Statistically significant differences in favor of losmapimod were observed, however, for several secondary endpoints of emotional, physical, and social functioningOswestry Disability Index; Profile of Mood States total score; Short-Form 36 Health Survey physical functioning, bodily pain, general health, role emotional, social functioning, and vitality domains; and Short-Form 36 physical, and mental components. There were no unexpected findings related to safety or tolerability following treatment with losmapimod. DISCUSSION:Losmapimod could not be differentiated from placebo in terms of analgesia. 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A double-blind, randomized, placebo-controlled study was undertaken to evaluate the analgesic efficacy of losmapimod (GW856553), a novel p38α/β inhibitor, in patients with chronic neuropathic pain due to lumbosacral radiculopathy. MATERIALS AND METHODS:A total of 144 patients with at least moderate baseline pain intensity (average daily score of ≥4 on an 11-point pain intensity numeric rating scale) were randomized to receive losmapimod, 7.5 mg bid orally or placebo. All patients underwent a blinded placebo run-in period for 7 days before receiving losmapimod/placebo for 28 days. Efficacy and safety evaluations were undertaken weekly. RESULTS:The adjusted mean treatment difference for the change from baseline to week 4 in numeric rating scale was −0.36 U (95% confidence interval, −0.84, 0.13; P=0.149) in favor of losmapimod over placebo; this was not considered clinically meaningful. Statistically significant differences in favor of losmapimod were observed, however, for several secondary endpoints of emotional, physical, and social functioningOswestry Disability Index; Profile of Mood States total score; Short-Form 36 Health Survey physical functioning, bodily pain, general health, role emotional, social functioning, and vitality domains; and Short-Form 36 physical, and mental components. There were no unexpected findings related to safety or tolerability following treatment with losmapimod. DISCUSSION:Losmapimod could not be differentiated from placebo in terms of analgesia. The lack of response could reflect insufficient losmapimod levels in the spinal cord or differences between lumbosacral radiculopathy and animal models of neuropathic pain.</abstract><cop>United States</cop><pub>Copyright Wolters Kluwer Health, Inc. All rights reserved</pub><pmid>25751578</pmid><doi>10.1097/AJP.0000000000000122</doi><tpages>11</tpages></addata></record>
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subjects Adolescent
Adult
Aged
Analgesics - therapeutic use
Cyclopropanes - therapeutic use
Double-Blind Method
Europe
Female
Follow-Up Studies
Humans
Male
Middle Aged
Neuralgia - drug therapy
Neuralgia - etiology
Pain Measurement
Physical Examination
Pyridines - therapeutic use
Radiculopathy - complications
Treatment Outcome
Young Adult
title A Randomized, Placebo-controlled Trial of the Analgesic Efficacy and Safety of the p38 MAP Kinase Inhibitor, Losmapimod, in Patients With Neuropathic Pain From Lumbosacral Radiculopathy
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