Tanezumab for chronic low back pain: a long-term, randomized, celecoxib-controlled Japanese Phase III safety study

被引:4
|
作者
Konno, Shin-Ichi [1 ]
Nikaido, Takuya [1 ]
Markman, John D. [2 ]
Ohta, Makoto [3 ]
Machida, Toshiya [3 ]
Isogawa, Naoki [3 ,6 ]
Yoshimatsu, Hiroki [3 ]
Viktrup, Lars [4 ]
Brown, Mark T. [5 ]
West, Christine R. [5 ]
Verburg, Kenneth M. [5 ]
机构
[1] Fukushima Med Univ, Dept Orthopaed Surg, Fukushima 9601295, Japan
[2] Univ Rochester, Dept Neurosurg, Translat Pain Res Program, Med Ctr, Rochester, NY 14618 USA
[3] Pfizer R&D Japan, Tokyo 1518589, Japan
[4] Eli Lilly & Co, Neurosci Business Unit, Indianapolis, IN 46225 USA
[5] Pfizer Inc, Pfizer Global Prod Dev, Groton, CT 06340 USA
[6] UCB Japan Co Ltd, Tokyo 1600023, Japan
关键词
celecoxib; chronic low back pain; efficacy; Japan; randomized clinical trial; safety; tanezumab; EFFICACY; KNEE; OSTEOARTHRITIS; PREVALENCE; NEURONS; EVENTS; TRIALS; HIP;
D O I
10.2217/pmt-2021-0040
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Aim & methods: This trial investigated long-term (56-week treatment/24-week follow-up) use of subcutaneous tanezumab (5 or 10 mg every 8 weeks) or oral celecoxib (200 mg/day) in Japanese patients with chronic low back pain. Results & conclusion: Tanezumab safety was consistent with previous studies, except overall adverse events (tanezumab 5 mg = 63.0%, tanezumab 10 mg = 54.8%, celecoxib = 67.4%) and events of abnormal peripheral sensation (tanezumab 5 mg = 9.8%, tanezumab 10 mg = 4.3%, celecoxib = 4.3%) were more frequent with 5 mg than 10 mg tanezumab. Joint safety event rates were 1.1% for tanezumab 5 mg, 2.2% for tanezumab 10 mg and 0% for celecoxib. All treatments improved pain and function throughout the treatment period. Lay abstract: In this study, researchers looked at the safety of tanezumab (a medication that blocks nerve growth factor) in Japanese people with chronic low back pain (CLBP). Researchers also looked at how well tanezumab improves the symptoms (pain and difficulty doing activities) of CLBP. People in the study were given oral (taken by mouth) celecoxib (a medication commonly used to treat CLBP) or injections of tanezumab (5 or 10mg doses) under the skin of the belly or upper leg every 8 weeks for a total of 56 weeks. Side effects (something expected or unexpected that people experienced during the study that may or may not be due to the medication they received) occurred in 63.0% of people receiving tanezumab 5 mg, 54.8% of people receiving tanezumab 10 mg and 67.4% of patients receiving celecoxib. More people receiving tanezumab 5 mg (9.8% of people) had a side effect related to abnormal peripheral sensation (tingling, burning, numbness or sensitivity to heat or cold hands or feet) than people receiving tanezumab 10 mg (4.3% of people) or celecoxib (4.3% of people). More people receiving tanezumab (5 mg = 1.1% of people, 10 mg = 2.2% of people) had a problem with one of their joints (knees or hips) during the study than people receiving celecoxib (0% of people). All treatments improved pain and the ability to do activities. Overall, the researchers concluded that tanezumab was well tolerated in most people and may improve the symptoms of CLBP.
引用
收藏
页码:323 / 335
页数:13
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