CTRI/2021/10/037098招募中2 期
A 5-year, randomized, double blind, placebo-controlled, multi-center study assessing the efficacy, safety, and tolerability of intra-articular regimens of LNA043 versus placebo in patients with symptomatic knee osteoarthritis (ONWARDS) - ONWARDS
ovartis Healthcare Pvt Ltd0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Body mass index (BMI) < 40 kg/m2
- •Diagnosis of primary tibiofemoral knee OA by standard American College of Rheumatology clinical and radiographic criteria
- •Radiographic disease K-L grade 2 or 3 knee OA with a predominantly medial TFC involvement defined as medial Joint Space Narrowing (medJSN) 1-2 and medJSN > lateral Joint Space Narrowing (latJSN) in the target knee
- •Participants with double baseline WOMAC Pain of 20-45 (out of 50) for the target knee after discontinuation of analgesics, anti-inflammatories and or low potency opioids within 48 hours or an equivalent of 5Ã?â??T1/2 wash out period (whichever is longer)
- •Symptomatic OA with pain in the target knee for at least 6 months
- •Primary source of pain throughout body is due to OA in the target knee: Widespread Pain Index score of ââ?°Â¤6 and a Symptom Severity score of <7
排除标准
- •Participants with radiographic knee OA K-L grade 4 on the non-target knee
- •Participants with WOMAC Pain > 15 (out of 50) in the non-target knee
- •Severe malalignment ( >7.5Ã?° varus or valgus) in the anatomical axis of the target knee
- •Clinical signs of moderate-severe inflammation (i.e., redness, warmth, effusion) of the target knee or requiring aspiration in the target knee within 12 weeks prior to Screening
- •Arthroscopy of the target knee within the 6 months prior to Screening
- •Previous surgical treatment of the target knee using mosaicplasty, microfracture, meniscectomy >50% or osteotomy, partial or complete joint replacement or planned knee surgery for either knee during the study
- •Unstable target knee joint (including, but not limited to, posttraumatic or congenital laxity) or insufficiently reconstructed ligaments based on medical history and/or physical examination by the Investigator
- •Other pathologies affecting the knee, including subchondral insufficiency fractures, bone fracture (acute or subacute in less than 6 months prior to screening) or bone bruise, osteonecrosis, malignant bone marrow infiltration, solid tumors, and/or patellofemoral dysplasia based on clinical assessment, X-ray or MRI
- •Symptomatic hip OA on either hip or hip prosthesis recently implanted (within 1 year) or foreseen within the study period (either hip)
- •1Other pain conditions that could confound assessments of the pain associated with knee OA
研究者
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