VER-01 Shows Enhanced Gastrointestinal Tolerability, Superior Pain Relief, and Improved Sleep Quality Compared to Opioids in Treating Chronic Low Back Pain: A Randomized Phase 3 Clinical Trial.

IF 3.3 2区 医学 Q1 CLINICAL NEUROLOGY
Winfried Meissner, Charles Argoff, Sabine Sator, Volker Schoder, Matthias Karst
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引用次数: 0

Abstract

Introduction: Chronic low back pain (CLBP) affects over half a billion people worldwide. Current pharmacologic treatments, comprising mainly non-steroidal anti-inflammatory drugs and opioids, offer limited efficacy and pose significant risks, warranting the development of tolerable, safe and effective alternatives.

Methods: This randomized controlled trial on adults with CLBP was designed to confirm the superior efficacy and gastrointestinal tolerability of VER-01, a novel, standardized full-spectrum extract from Cannabis sativa DKJ127 L., over opioids. Subjects were randomized (1:1) to receive VER-01 or a range of commercially available opioids. After a 3-week titration, subjects underwent 24 weeks of treatment, followed by 2 weeks of wash-out. The primary endpoint was the relative risk of constipation occurrence after 27 weeks treatment. Secondary endpoints included changes in pain and sleep scores, determined using an 11-point numeric rating scale (NRS), with key secondary endpoints defined for week 27.

Results: A total of 384 individuals were randomized to receive VER-01 (n = 192) or opioids (n = 192). Subjects receiving VER-01 were fourfold less likely to develop constipation than those receiving opioids (relative risk [RR] VER-01/opioids 0.25; 95% confidence interval [CI] 0.09-0.69; p = 0.007) and threefold less likely to use laxatives (RR 0.34; 95% CI 0.18-0.65; p < 0.001). Longitudinal analysis revealed that VER-01 was superior to opioids in terms of pain reduction over 6 months of treatment, although differences in secondary endpoints limited to week 27 alone were not significant. Throughout the 6 months of treatment, mean pain reduction was 2.50 NRS points with VER-01 versus 2.16 with opioids (mean difference [MD] 0.34; 95% CI 0.00-0.67; p = 0.048), and sleep improved by 2.52 points with VER-01 versus 2.07 with opioids (MD 0.45; 95% CI 0.11-0.79; p = 0.009). These benefits were particularly pronounced in participants with severe pain, with greater pain reduction (MD 0.58; 95% CI 0.01-1.15) and sleep improvement (MD 0.66, 95% CI 0.05-1.27) compared to opioids.

Conclusions: VER-01 demonstrated superiority over opioids in treating CLBP, both in terms of efficacy and gastrointestinal tolerability.

Trial registration: ClinicalTrials.gov ID: NCT05610813; EudraCT ID: 2022-001358-41.

与阿片类药物相比,VER-01在治疗慢性腰痛方面显示出增强的胃肠道耐受性,更好的疼痛缓解和改善的睡眠质量:一项随机3期临床试验
慢性腰痛(CLBP)影响着全球超过5亿人。目前的药物治疗主要包括非甾体类抗炎药和阿片类药物,其疗效有限且存在重大风险,因此需要开发可耐受、安全和有效的替代品。方法:这项针对CLBP成人患者的随机对照试验旨在证实VER-01优于阿片类药物的疗效和胃肠道耐受性。VER-01是一种新型、标准化的大麻全谱提取物DKJ127 L.。受试者被随机(1:1)接受VER-01或一系列市售阿片类药物。3周滴定后,受试者接受24周治疗,随后进行2周洗脱。主要终点是治疗27周后便秘发生的相对风险。次要终点包括疼痛和睡眠评分的变化,使用11分数字评定量表(NRS)确定,关键次要终点为第27周。结果:384例患者随机接受VER-01治疗(n = 192)或阿片类药物治疗(n = 192)。接受VER-01治疗的受试者发生便秘的可能性比接受阿片类药物治疗的受试者低4倍(相对危险度[RR] VER-01/阿片类药物0.25;95%可信区间[CI] 0.09-0.69; p = 0.007),使用泻药的可能性低3倍(RR 0.34; 95% CI 0.18-0.65; p结论:VER-01在治疗CLBP方面的疗效和胃肠道耐受性均优于阿片类药物。试验注册:ClinicalTrials.gov ID: NCT05610813;草案编号:2022-001358-41。
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来源期刊
Pain and Therapy
Pain and Therapy CLINICAL NEUROLOGY-
CiteScore
6.60
自引率
5.00%
发文量
110
审稿时长
6 weeks
期刊介绍: Pain and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of pain therapies and pain-related devices. Studies relating to diagnosis, pharmacoeconomics, public health, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to, acute pain, cancer pain, chronic pain, headache and migraine, neuropathic pain, opioids, palliative care and pain ethics, peri- and post-operative pain as well as rheumatic pain and fibromyalgia. The journal is of interest to a broad audience of pharmaceutical and healthcare professionals and publishes original research, reviews, case reports, trial protocols, short communications such as commentaries and editorials, and letters. The journal is read by a global audience and receives submissions from around the world. Pain and Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an international and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of all scientifically and ethically sound research.
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