跳至主要内容
临床试验/2025-520479-25-00
2025-520479-25-00招募中3 期

A Phase 3, Multicenter, Double-Blinded, Randomized Study to Evaluate REGN7508, a Factor XI Monoclonal Antibody, Versus Acetylsalicylic Acid for Prophylaxis of Symptomatic Venous Thromboembolism After Elective Total Knee Arthroplasty (ROXI-ASPEN)

Regeneron Pharmaceuticals Inc.11 个研究点 分布在 3 个国家目标入组 208 人开始时间: 2025年12月5日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
208
试验地点
11
主要终点
Incidence of the composite endpoint of symptomatic VTE and VTE-related death

研究概览

简要总结

To evaluate the efficacy of IV REGN7508 for the prevention of symptomatic VTE after TKA compared to ASA

入排标准

年龄范围
18 years 至 65+ years(18-64 Years, 65+ Years)
接受健康志愿者

入选标准

  • Is undergoing a primary elective unilateral TKA.
  • Is in good health based on laboratory safety testing as described in the protocol
  • Other protocol-defined Inclusion criteria apply

排除标准

  • Has any condition that, as assessed by the investigator, may confound the results of the study or pose an additional risk to the participant by study participation.
  • Has a history of bleeding in the 6 months prior to randomization requiring hospitalization or transfusion; history of intracranial or intraocular bleeding, excessive operative or post-operative bleeding, and traumatic spinal or epidural anesthesia; history of bleeding diathesis (eg, hemophilia A or B, von Willebrand’s Factor deficiency).
  • Has a history of thromboembolic disease or thrombophilia.
  • Has a history of platelet dysfunction.
  • Has received or plans to receive preoperative enoxaparin on the day prior to TKA surgery
  • Other protocol-defined Exclusion criteria apply

研究组 & 干预措施

REGN7508

Test

干预措施: REGN7508 (Drug)

Placebo for REGN7508

Placebo

干预措施: Placebo for REGN7508 (Drug)

Placebo for Acetylsalicylic Acid

Placebo

干预措施: Placebo for Acetylsalicylic Acid (Drug)

ACETYLSALICYLIC ACID

Comparator

干预措施: ACETYLSALICYLIC ACID (Drug)

结局指标

主要结局

Incidence of the composite endpoint of symptomatic VTE and VTE-related death

Incidence of the composite endpoint of symptomatic VTE and VTE-related death

次要结局

  • Incidence of confirmed symptomatic Deep Vein Thrombosis (DVT)
  • Incidence of confirmed Pulmonary Embolism (PE)
  • Incidence of VTE-related death
  • Time to first event of the composite endpoint of symptomatic VTE and VTE-related death
  • Time to first event of confirmed symptomatic DVT
  • Time to first event of confirmed PE
  • Time to VTE-related death
  • Incidence of the composite endpoint of major bleeding and Clinically Relevant Non-Major (CRNM) bleeding
  • Incidence of minor bleeding
  • Incidence of Treatment-Emergent Adverse Events (TEAEs)
  • Severity of TEAEs
  • Incidence of Anti-drug Antibody (ADA) to REGN7508
  • Magnitude of ADA to REGN7508
  • Concentrations of REGN7508

研究者

发起方
Regeneron Pharmaceuticals Inc.
申办方类型
Pharmaceutical company
责任方
Principal Investigator
主要研究者

Medical Affairs

Scientific

Regeneron Pharmaceuticals Inc.

研究点 (11)

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