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A Phase I, Dose Escalation, Open-label, Multicenter Study of EA5 Injection in Adults With APS and Recurrent Thrombosis

2026年6月2日 更新者:Shanghai Lanyi Therapeutics Co., Ltd.

A Phase I, Dose Escalation, Open-label, Multicenter Clinical Study to Evaluate the Safety, Tolerability, Preliminary Efficacy, Pharmacodynamics, and Pharmacokinetics of EA5 Injection in Adult Participants With Antiphospholipid Syndrome (APS) and Recurrent Thrombosis Under Standard-of-Care Background Therapy

This is a Phase I, open-label, dose escalation, multicenter study to evaluate the safety, tolerability, preliminary efficacy, pharmacodynamics (PD), and pharmacokinetics (PK) of EA5 injection in adult participants with Antiphospholipid Syndrome (APS) and recurrent thrombosis who are receiving standard-of-care antithrombotic therapy. Approximately 12 participants will be enrolled. The whole study treatment cycle was 24 weeks. Administration of low-dose EA5: First, administer the loading dose regimen intravenously, then maintain administration subcutaneously every 2 weeks(Q2W). Administration of high-dose EA5: First, administer the loading dose regimen intravenously, then maintain administration subcutaneously every 2 weeks(Q2W).The primary objective is to assess safety and tolerability. Secondary objectives include evaluation of preliminary efficacy, immunogenicity, PK, PD (complement inhibition), and APS-related biomarker changes.

研究概览

地位

主动,不招人

干预/治疗

研究类型

介入性

注册 (估计的)

12

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Beijing Municipality
      • Beijing、Beijing Municipality、中国、100044
        • Peking University People's Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Participants must be ≥18 years of age at the time of signing the Informed Consent Form (ICF).
  2. Participants diagnosed with Antiphospholipid Syndrome (APS) according to the 2023 EULAR/ACR classification criteria, with at least two of the three antiphospholipid antibodies positive: anticardiolipin antibody (aCL), anti-β2-glycoprotein I antibody (anti-β2GPI), and lupus anticoagulant (LA).
  3. Experienced ≥2 thrombotic events within the past 5 years under antithrombotic prophylactic therapy, confirmed by objective imaging.
  4. Stable antithrombotic treatment regimen for at least 6 months prior to screening (dose adjustment of warfarin to achieve a stable INR is permitted).
  5. Vaccination against Neisseria meningitidis (MPV-ACYW) within <3 years prior to initiation of study treatment; OR if not previously vaccinated, receipt of the meningococcal vaccine (MPV-ACYW) at least 14 days prior to the first dose of the investigational product. If the vaccine is administered within 14 days before dosing, antibiotic prophylaxis must be provided until 2 weeks post-vaccination.
  6. Vaccination against Streptococcus pneumoniae according to national vaccination recommendations (e.g., Advisory Committee on Immunization Practices [ACIP] guidelines). OR if not previously vaccinated, receipt of the pneumococcal vaccine at least 14 days prior to the first dose of the investigational product. If the vaccine is administered within 14 days before dosing, antibiotic prophylaxis must be provided until 2 weeks post-vaccination.
  7. Use of contraception by men and women should be consistent with local regulations regarding contraceptive methods for clinical trial participants.

(1)Male Participants: Male participants must agree to use effective contraception during the treatment period and for at least 6 months after the last dose of the study intervention, and to refrain from donating sperm during this time.

(2)Female Participants: Non-pregnant, non-lactating female participants are eligible to participate if they meet at least one of the following conditions: use of an effective or acceptable contraceptive method during the treatment period and for at least 6 months after the last dose of the study drug.

Capable of understanding the study procedures and methods, willing to sign the ICF, and able to strictly adhere to the clinical study protocol to complete the study.

Exclusion Criteria:

  1. History of malignancy within 5 years prior to screening and before administration (except for localized skin basal cell carcinoma, squamous cell carcinoma, or cervical carcinoma in situ that have undergone curative local treatment with no evidence of metastasis in the past 3 years).
  2. Thrombosis with other definite etiologies, such as malignancy, hereditary thrombophilia, thrombotic microangiopathy, etc.
  3. History of catastrophic antiphospholipid syndrome (i.e., progressive thrombosis in multiple [3 or more] organs occurring within 1 week, involving critical organs such as the brain, kidneys, liver, or heart leading to failure, with pathological confirmation of small vessel thrombosis).
  4. Presence of active bleeding or high risk of bleeding, such as gastrointestinal bleeding, intracranial bleeding, respiratory tract bleeding, coagulation disorders, etc.
  5. History of major surgery within 1 month prior to screening or requiring major elective surgery during the trial period.
  6. History of immunodeficiency, including a positive test for human immunodeficiency virus (HIV) antibody, or having other acquired or congenital immunodeficiency diseases.
  7. Comorbid with systemic autoimmune diseases (e.g., systemic lupus erythematosus, systemic sclerosis, etc.).
  8. Unresolved meningococcal infection.
  9. Positive for hepatitis C virus (HCV) antibody at screening (except for those with a negative HCV RNA result), positive for human immunodeficiency virus (HIV) antibody, positive for anti-Treponema pallidumantibody (TP-Ab) (except for those with a negative RPR or TRUST test), OR positive for hepatitis B virus (HBV) surface antigen (HBsAg) (except for those with an HBV DNA level ≤ 1000 IU/mL).
  10. Presence of active infection requiring systemic therapy within 4 weeks prior to the first use of the investigational product (including herpes zoster, active tuberculosis, active Treponema palliduminfection, and fungal infections requiring systemic therapy).
  11. Participants with severe hepatic or renal impairment: Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≥ 3 times the upper limit of normal (ULN); total bilirubin ≥ 2 times ULN; serum creatinine ≥ 2.5 times ULN, OR calculated creatinine clearance ≤ 30 mL/min according to the Cockcroft-Gault formula.
  12. Receipt of other interventional therapy or participation in another clinical study within 30 days prior to the first use of the investigational product or within 5 half-lives of this investigational product (whichever is longer).
  13. Prior use of complement C3 or C5 targeted therapy.
  14. History of allergy to any component of EA5, including hypersensitivity to human, humanized, or murine monoclonal antibodies, or known hypersensitivity to any ingredient of the product.
  15. Any disease that, in the opinion of the investigator or sponsor, may increase participant risk or confound study outcomes. Including, but not limited to, significant circulatory, respiratory, urinary, endocrine system diseases, etc.
  16. Female participants who are pregnant or breastfeeding.
  17. Any other condition for which the investigator considers the participant unsuitable to enter this clinical study.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:非随机化
  • 介入模型:顺序分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Cohort 1
Queue 1: Administration of low-dose EA5 First, administer the loading dose regimen intravenously, then maintain administration subcutaneously every 2 weeks(Q2W).
Administer the loading dose regimen intravenously, then maintain administration subcutaneously
实验性的:Cohort 2
Queue 2: Administration of high-dose EA5 First, administer the loading dose regimen intravenously, then maintain administration subcutaneously every 2 weeks(Q2W).
Administer the loading dose regimen intravenously, then maintain administration subcutaneously

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Number of Participants With Treatment Emergent Adverse Events (TEAEs)
大体时间:Baseline up to Week28
TEAEs were defined as AEs that occurred on or after the date and time of study drug administration, or those that first occurred before dosing but worsened in frequency or severity after study drug administration. A summary of all Serious Adverse Events and Other Adverse Events (nonserious) regardless of causality is located in the 'Reported Adverse Events' Section.
Baseline up to Week28

次要结果测量

结果测量
措施说明
大体时间
Number of participants with adjudicated thrombotic events during the treatment period (including venous, arterial, and small-vessel thrombotic events)
大体时间:Baseline up to Week28
Baseline up to Week28
Number of adjudicated thrombotic events per participant
大体时间:Baseline up to Week28
Baseline up to Week28
Change in annualized thrombosis event rate compared to baseline (the 5-year period prior to treatment)
大体时间:Baseline up to Week28
Baseline up to Week28
Change in platelet count from baseline at each visit
大体时间:Baseline up to Week28
Baseline up to Week28
Situations requiring adjustment of antithrombotic treatment regimen during the treatment period
大体时间:Baseline up to Week28
Baseline up to Week28
Change in levels of sC5b-9 before and after dosing
大体时间:Baseline up to Week28
Baseline up to Week28
Change in levels of free C5 before and after dosing
大体时间:Baseline up to Week28
Baseline up to Week28
Incidence of anti-drug antibodies (ADA) against the humanized monoclonal antibody EA5
大体时间:Baseline up to Week28
Baseline up to Week28
Maximum Observed Serum Concentration (Cmax) of EA5
大体时间:Baseline up to Week28
Blood samples were collected for analysis of Cmax
Baseline up to Week28
Time To Maximum Observed Serum Concentration (Tmax) of EA5
大体时间:Baseline up to Week 28
Blood samples were collected for analysis of Tmax
Baseline up to Week 28
Area Under The Serum Concentration Versus Time Curve From Time Zero To The Time of The Last Quantifiable Concentration (AUC0-t) of EA5
大体时间:Baseline up to Week 28
Blood samples were collected for analysis of AUC0-t
Baseline up to Week 28
Terminal Elimination Rate Constant (λz) of Serum EA5
大体时间:Baseline up to Week 28
Blood samples were collected for analysis of λz
Baseline up to Week 28
Terminal Elimination Half-life (t½) of Serum EA5
大体时间:Baseline up to Week 28
Blood samples were collected for analysis of t½
Baseline up to Week 28
Total Clearance (CL) of EA5
大体时间:Baseline up to Week 28
Blood samples were collected for analysis of CL
Baseline up to Week 28

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年5月25日

初级完成 (估计的)

2027年9月30日

研究完成 (估计的)

2027年12月31日

研究注册日期

首次提交

2026年5月28日

首先提交符合 QC 标准的

2026年6月2日

首次发布 (实际的)

2026年6月8日

研究记录更新

最后更新发布 (实际的)

2026年6月8日

上次提交的符合 QC 标准的更新

2026年6月2日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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