Interpath Pty LTD, 10 Skipton Street, Ballarat, VIC, 3350, Australia.
Vedic Lifesciences, Mumbai, India.
Inflammopharmacology. 2022 Aug;30(4):1323-1334. doi: 10.1007/s10787-022-01013-y. Epub 2022 Jun 22.
To explore the safety, and efficacy of a proprietary hydrolyzed oil extract from seeds of Biota orientalis (hBO/Epiitalis, Interpath Pty Ltd) in patients with knee pain due to osteoarthritis (OA).
Patients aged 40-65 with X-ray diagnosed knee OA and knee pain ≥ 60 on a 100-point VAS (visual analog scale) were enrolled and randomized into four groups to receive daily hBO for 56 days as high (hBO-HD, 640 mg), mid (hBO-MD, 320 mg) or low (hBO-LD, 160 mg) doses, or a matched placebo oil. The primary outcome was change in VAS knee pain from baseline to 56 days in the mITT (modified intention to treat) population. Exploratory outcomes were the mWOMAC (modified Western Ontario and McMaster Universities Arthritis Index), and the SF-36 QoL (quality of life) questionnaire. The OMERACT-OARSI (Outcome Measures in Arthritis Clinical Trials-Osteoarthritis Research Society International) responder index was also calculated.
223 patients were included in the mITT population. Reductions in VAS scores between baseline and day 56 [Least square mean (LS mean) and 95% confidence interval (CI) of LS mean] were 36.4 (31.7-41.0), 37.9 (33.2-42.7), 35.7 (31.2-40.1) and 9.8 (14.5-15.2) for the hBO-HD, hBO-MD, hBO-LD, and placebo groups respectively. The VAS changes in all hBO groups were significantly different (p < 0.0001) vs. changes in the placebo group. hBO treatment led to similar quantitative beneficial changes in mWOMAC, SF-36 and OMERACT-OARSI responder index. There were no SAEs and no adverse events ascribed to the intervention.
In a 56-day trial, hBO was safe, and was efficacious at reducing symptoms in patients with knee OA.
NCT04117490; Oct 7, 2019.
探索从东方生物种子中提取的专利水解油(hBO/Epiitalis,Interpath Pty Ltd)在膝骨关节炎(OA)患者膝痛中的安全性和疗效。
招募年龄在 40-65 岁之间、X 线诊断为膝 OA 且膝关节疼痛≥100 分视觉模拟量表(VAS)的患者,并将其随机分为 4 组,分别接受 56 天的高剂量(hBO-HD,640mg)、中剂量(hBO-MD,320mg)、低剂量(hBO-LD,160mg)或匹配安慰剂油的每日治疗。主要结局是在意向治疗人群(mITT)中从基线到 56 天 VAS 膝关节疼痛的变化。探索性结局是 mWOMAC(改良的西安大略和麦克马斯特大学关节炎指数)和 SF-36 QoL(生活质量)问卷。还计算了 OMERACT-OARSI(关节炎临床试验中的结局测量-骨关节炎研究协会国际)反应指数。
223 例患者纳入 mITT 人群。与基线相比,第 56 天 VAS 评分的降低[最小二乘均值(LS 均值)和 LS 均值的 95%置信区间(CI)]分别为 36.4(31.7-41.0)、37.9(33.2-42.7)、35.7(31.2-40.1)和 9.8(14.5-15.2),分别为 hBO-HD、hBO-MD、hBO-LD 和安慰剂组。所有 hBO 组的 VAS 变化均与安慰剂组的变化有显著差异(p<0.0001)。hBO 治疗导致 mWOMAC、SF-36 和 OMERACT-OARSI 反应指数的类似定量有益变化。没有出现严重不良事件,也没有将不良事件归因于干预措施。
在为期 56 天的试验中,hBO 安全且有效,可减轻膝骨关节炎患者的症状。
NCT04117490;2019 年 10 月 7 日。