NWRD09 for Persistent Cervical HPV16 Infection
A Randomized, Double-Blind, Placebo-Controlled Clinical Study Evaluating the Efficacy and Safety of NWRD09 in Patients With Persistent Cervical HPV16 Infection
研究概览
详细说明
This is a randomized, double-blind, placebo-controlled clinical trial designed to evaluate the efficacy and safety of NWRD09 in patients with persistent cervical HPV16 infection who may or may not have concomitant cervical LSIL. Eligible participants will be randomized in a 1:1 ratio to two groups: NWRD09 and placebo.
Participants will receive intramuscular injections of either NWRD09 or placebo at the corresponding dose at weeks 0, 2, 4, and 12 (a total of 4 doses).
Efficacy evaluations at Week 16 will include cervical cytology and HPV testing.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Jian Zhao, M.D.
- 电话号码:+86-15601199333
- 邮箱:854496@qq.com
学习地点
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Beijing、中国
- 招聘中
- Peking University First Hospital
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Female, aged 45 to 65 years (inclusive).
- Documented positive result for HPV 16 from a cervical sample collected at screening, with a confirmed duration of positivity for at least 12 months before screening.
- Satisfactory colposcopy examination. For participants with concomitant cervical LSIL, the entire aceto-white staining area or the suspected cervical intraepithelial neoplasia (CIN) lesion, including the upper border of the transformation zone, must be fully visualized.
- Adequate organ function within 1 week before the first dose, defined as:
1) Hematology: Hemoglobin (Hb) ≥ 100 g/L; Platelet count (PLT) ≥ 75 × 10⁹/L; Absolute neutrophil count (ANC) ≥ 1.5 × 10⁹/L.
2) Hepatic: Total bilirubin (TB) ≤ 1.5 × Upper Limit of Normal (ULN); Alanine aminotransferase (ALT) and Aspartate aminotransferase (AST) ≤ 1.5 × ULN; Plasma albumin ≥ 30 g/L.
3) Renal: Serum creatinine (Scr) ≤ 1.5 × ULN, or calculated creatinine clearance ≥ 60 mL/min (using the Cockcroft-Gault formula) [for participants with serum creatinine > 1.5 × ULN].
(5) For premenopausal women of childbearing potential: a negative serum pregnancy test within 7 days before the first dose. Eligible participants of childbearing potential and their partners must agree to use highly effective contraception throughout the trial and for 6 months after the last study dose (at Week 12).
(6) Ability to understand the study and voluntarily provide written informed consent (ICF), willingness and ability to communicate effectively with the investigator, and to comply with all protocol-required treatment, examinations, and visits.
Exclusion Criteria:
- Any histopathologically confirmed cervical adenocarcinoma/adenocarcinoma in situ (AIS), high-grade cervical, vulvar, vaginal, or anal intraepithelial neoplasia, or invasive cancer.
- Cervical cytology results indicating ASC-H (Atypical Squamous Cells - cannot exclude HSIL), HSIL (High-grade Squamous Intraepithelial Lesion), SCC (Squamous Cell Carcinoma), AGC (Atypical Glandular Cells), or AIS; *Exception: Participants with ASC-H or HSIL may be enrolled if histopathological evidence confirms no lesion or CIN1, upon investigator's assessment.*.
- Pregnant or lactating women, or individuals planning to conceive during the study period.
- Participation in another clinical trial within 30 days before screening, or currently within the observational follow-up period of another clinical trial.
- Continuous systemic corticosteroid therapy (at a dose equivalent to >10 mg/day of prednisone) for more than one week within 30 days before screening; Exceptions: Hormone replacement therapy, and local administration (e.g., intra-tracheal, ocular).
- Continuous use of immunosuppressants (e.g., cyclosporine, tacrolimus, azathioprine, 6-mercaptopurine, antilymphocyte globulin) for more than one week within 30 days before screening.
- Administration of any non-live vaccine within 4 weeks, or any live vaccine within 4 weeks, before the first dose.
- History of receiving any therapeutic HPV vaccination; Note: Vaccination with approved prophylactic HPV vaccines is acceptable.
- Use of blood or blood-derived products (including immunoglobulins) within 3 months before the first dose, or planned use during the study period.
- History of immunodeficiency or autoimmune diseases (e.g., rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis).
- Current or anticipated use during the study period of disease-modifying antirheumatic drugs (e.g., azathioprine, cyclophosphamide, cyclosporine, methotrexate) or biologic disease-modifying agents (e.g., infliximab, adalimumab, etanercept).
- History of solid organ or bone marrow transplantation.
- History or current diagnosis of other malignancies.
- Presence of active infection requiring systemic therapy (including active tuberculosis, active syphilis, and bacterial, fungal, or viral infections requiring systemic treatment).
- Positive test results for any of the following: Hepatitis B surface antigen (HBsAg), Hepatitis C virus antibody (anti-HCV), Treponema pallidum antibody (TP-Ab), or Human Immunodeficiency Virus antibody (anti-HIV).
- Known history of allergy to any component of the investigational product or similar drugs; or history of severe allergy to any food, drug, or other substances (e.g., urticaria, eczema, dyspnea, angioedema).
- Severe dysfunction of other organs or severe cardiopulmonary disease.
- Presence of tattoos, scars, or active lesions/rashes within a 2 cm radius of the intended injection site (deltoid muscle) that may interfere with safety assessment.
- Known psychiatric disorders or substance abuse disorders that may interfere with the subject's ability to comply with study requirements.
- Any condition, therapy, laboratory abnormality, history of other circumstances, or current evidence that, in the investigator's judgment, may increase the risk associated with study participation or investigational product administration, may interfere with the interpretation of study results, or render the participant unsuitable for enrollment in this study.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:四人间
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:NWRD09
Each participant will be administered NWRD09 by IM injection at weeks 0, 2, 4, and 12.
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NWRD09/ Placebo
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安慰剂比较:Placebo
Each participant will be administered placebo by IM injection at weeks 0, 2, 4, and 12.
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NWRD09/ Placebo
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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 |
|---|---|---|
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Proportion of participants with virologically-proven clearance of HPV 16 at week 16.
大体时间:Week 16
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The number of participants with virologically-proven clearance of HPV 16 at week 16.
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Week 16
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Incidence and severity of local and systemic adverse events (AEs).
大体时间:up to 36 weeks
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Based on the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) V5.0, adverse events (AEs) and serious adverse events (SAEs) will be monitored.
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up to 36 weeks
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Proportion of participants with virologically-proven clearance of HPV 16 at week 28.
大体时间:Week 28
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The number of participants with virologically-proven clearance of HPV 16 at week 28.
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Week 28
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Proportion of participants with virologically-proven clearance of HPV 16 at weeks 16 and 28.
大体时间:Weeks 16、28
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The number of participants with virologically-proven clearance of HPV 16 at weeks 16 and 28.
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Weeks 16、28
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Proportion of participants with baseline cervical LSIL showing histopathological regression to no lesions at 28 weeks after the first dose.
大体时间:Week 28
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The number of participants with cervical LSIL showing histopathological regression to no lesions at week 28.
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Week 28
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Levels of cellular immune responses.
大体时间:Weeks 6, 16 , 28
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Levels of cellular immune responses measured by interferon-gamma enzyme-linked immunospot (IFN-γ ELISPOT) assay in peripheral blood mononuclear cells (PBMCs) of participants at baseline and at weeks 6, 16, 28.
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Weeks 6, 16 , 28
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
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)?
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研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
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