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Phase 1 Challenge Study Using rDEN2delta30-7169 to Evaluate Host-Pathogen Interactions in Primary, Homotypic, and Heterotypic Dengue Virus Infection

Background:

Dengue is a viral disease spread by mosquitoes. Most people bitten by mosquitoes carrying dengue viruses do not get sick, but severe cases can cause shock, internal bleeding, and death. There are no treatments for dengue. To develop treatments, researchers need to understand more about what dengue viruses do in the body.

Objective:

To infect healthy people with a mild dengue virus to study how their body responds.

Eligibility:

People ages 18 to 50 years with or without a history of dengue virus infection.

Design:

Participants will be screened. They will have a physical exam with blood tests. The tests will show whether they have ever been infected with dengue or related viruses in the past.

At their first study visit, participants will receive an injection of dengue virus into the arm. The injected virus is weaker than the natural virus, so any symptoms should be milder.

Participants will have a total of 11 study visits over 6 months; 8 of those visits will be in the first month. Blood will be drawn at each visit. Some visits will include ultrasound exams of their internal organs. They will discuss any symptoms they are having. Any rashes they develop may be photographed.

Two procedures are optional: Participants may have up to 5 lymph node aspirations and 3 bone marrow biopsies during the study. For both procedures, a needle will be inserted into the tissues to draw out immune cells.

Two more visits are optional: 1 visit up to 2 months before receiving the virus, for lymph node or bone marrow samples, and 1 about a year after for a blood draw....

研究概览

详细说明

Study Description:

This is a phase 1 challenge trial where healthy adults with no flavivirus antibodies (naive), dengue virus serotype 2 (DENV2)-dominant antibodies (homotypic), or non-DENV2-dominant antibodies (heterotypic) will be infected with the live attenuated DENV2 challenge strain rDEN2delta30-7169. We will evaluate the safety and immunogenicity of the challenge strain as well as how immune history influences IP-10 signaling, bone marrow cellularity, and the development of bone marrow DENV2-specific cells. Exploratory objectives include examining the immunological and clinical impact of homotypic and heterotypic infection, how viral replication affects the bone marrow and induces protective or dysregulated immune responses, and the determinants of long-lived immunity to inform dengue vaccines and therapeutics. We hypothesize that the challenge strain will be safe. The heterotypic group is predicted to have the highest viremia as measured by RNA (viral RNAemia) and boost in neutralizing antibodies, and the homotypic challenge group will have the lowest. We also expect that the heterotypic group will have the biggest changes in IP-10 signaling between days 0 and 19. During acute infection, we expect that the heterotypic and naive groups will have altered bone marrow cellularity such that it differs from the reference range, but the homotypic group will not have altered cellularity. At day 57, we expect that there will be DENV-specific antibody secreting cells in the bone marrow.

Primary Objective:

Evaluate the safety, viral RNAemia, and immunogenicity of rDEN2delta30-7169 in those with distinct DENV infection histories.

Secondary Objectives:

Compare chemokine signaling and the magnitude of DENV2-specific antibody-secreting cells in the bone marrow among groups. Evaluate the bone marrow cellularity during infection within each group.

Primary Endpoints:

  1. Safety: The frequency and severity of adverse events (AEs) through day 28 and serious adverse events (SAEs) through day 180 regardless of prior immune history.
  2. Viral RNAemia: Fold difference between groups in peak viral RNAemia titers on any day from days 2 to 19.
  3. Immunogenicity: Fold change in DENV1-4 neutralizing antibody geometric mean titers (GMTs) between days 0 and 28 within each group.

Secondary Endpoints:

  1. Differences in the change in IP-10 signaling between day 0 and days 2 to 19 among groups.
  2. Difference between the bone marrow cellularity at day 5 versus the reference range within each group.
  3. The magnitude of bone marrow DENV-specific antibody-secreting cells at day 57.

研究类型

介入性

注册 (估计的)

200

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。

学习联系方式

学习地点

    • Maryland
      • Bethesda、Maryland、美国、20892
        • 招聘中
        • National Institutes of Health Clinical Center
        • 接触:
          • NIH Clinical Center Office of Patient Recruitment (OPR)
          • 电话号码:TTY dial 711 (800) 411-1222
          • 邮箱:ccopr@nih.gov
        • 接触:

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

接受健康志愿者

是的

描述

  • INCLUSION CRITERIA:

To be eligible to participate in this study, an individual must meet all the following criteria:

  1. Aged 18 to 50 years.
  2. In good general health as evidenced by medical history, physical examination, and laboratory screening results
  3. Willing to allow storage of samples and data for future research.
  4. Willing to forgo receipt of any vaccine in the 28 days preceding the challenge strain through the 28 days following administration of the challenge strain. For participants opting for LN FNA or bone marrow sampling on day 57, they must be willing to forgo any vaccine through day 57. For those opting for FNA or bone marrow sampling on day 180, they must be willing to forgo any vaccine for at least 28 days before sampling.
  5. For individuals who can become pregnant: use of at least one method of effective contraception (see below) from at least 28 days prior to challenge through 60 days after challenge.
  6. Able to provide informed consent.
  7. Willing to adhere to lifestyle considerations for the duration of the study.
  8. Willing to avoid travel to a dengue-endemic area as defined by the CDC from 1 month before administration of challenge through day 28. For participants opting for LN FNA or bone marrow sampling on day 57, they must be willing to forgo travel through day 57.
  9. Serologic evidence of previous dengue virus infection consistent with our serology criteria.

    a. For the flavivirus-naive group, they must have no history of flavivirus vaccination or medical illness concerning for a flavivirus infection. If there is uncertainty about a previous flavivirus exposure, then confirmatory antibody testing against the virus of interest must be negative.

  10. Agree to avoid participation in other clinical studies requiring investigational interventions through day 180.
  11. Agree to avoid blood and plasma donation outside this study through day 57.

Contraceptive requirements: Participants who can become pregnant must agree to use at least one method of effective contraception as outlined below from at least 28 days before through 60 days after challenge to avoid any potential risk from the product on the pregnancy or fetus. Participants who can become pregnant must have a negative serum pregnancy test on day 0 before receiving rDEN2delta30-7169. If a participant becomes pregnant or suspects they are pregnant during the study, they should inform the study staff and their primary care physician immediately. Acceptable forms of contraception are listed below and are consistent with prior studies using this product:

  • Intrauterine device or equivalent.
  • Hormonal contraceptive (e.g., consistent, timely, and continuous use of contraceptive pill, patch, ring, implant, or injection that has reached full efficacy prior to challenge).
  • Condom, diaphragm, or cervical cap plus spermicide.
  • A stable, long-term monogamous relationship with a partner who does not pose any potential pregnancy risk, e.g., has undergone a vasectomy at least 6 months prior to administration of challenge strain or is of the same sex as the participant.
  • A hysterectomy and/or a bilateral tubal ligation, bilateral oophorectomy, or post-menopausal status defined as age >=45 years and at least 1 year since last menstrual period.

Participants who become pregnant after challenge but before day 180 will be excluded from any further research procedures. If the participant agrees, we will collect and report pregnancy outcomes through day 180, which is the final required study visit.

EXCLUSION CRITERIA:

An individual who meets any of the following criteria will be excluded from participation in this study:

  1. Pregnancy.
  2. Lactation during the first 28 days of the study.
  3. Baseline absolute neutrophil count (ANC) <=750 cells/microL.
  4. Baseline creatinine >=1.5 mg/dL.
  5. Baseline ALT >=1.25 x upper limit of normal.
  6. Requiring a potent anticoagulator like a direct acting oral agent or warfarin during the first 28 days of the study.
  7. History of or positive test result for HIV, hepatitis B, or hepatitis C.
  8. History of a tetravalent, chimeric, or subunit dengue vaccine.
  9. Has any of the following:

    1. More than 10 days of systemic immunosuppressive medications (>=10 mg prednisone dose or its equivalent) or cytotoxic medication within the 30 days prior to administration of challenge strain or immunomodulating therapy within 180 days prior to administration of challenge strain.
    2. Received blood products, including immunoglobulin products, within 120 days prior to administration of challenge strain.
    3. History of serious reactions to vaccines.
    4. Hereditary, acquired, or idiopathic forms of angioedema.
    5. Idiopathic urticaria within the past year.
    6. Asthma that is not well controlled or required emergency care, urgent care, hospitalization, or intubation during the past two years or that requires the use of oral or intravenous steroids.
    7. Type 1 or type 2 diabetes mellitus that is not well controlled (hemoglobin A1c >8).
    8. Clinically significant autoimmune disease or immunodeficiency.
    9. Blood pressure >=180/110 (stage 3 hypertension) on at least 2 measures.
    10. Documented diagnosis of a bleeding disorder (e.g., factor deficiency, coagulopathy, or platelet disorder requiring special precautions).
    11. Significant bruising or bleeding difficulties with subcutaneous injections or blood draws.
    12. Malignancy that is active or treated malignancy for which there is no reasonable assurance of sustained cure, or malignancy that is likely to recur during the study period.
    13. Asplenia or functional asplenia.
    14. Current alcohol or drug abuse or addiction.
  10. Any medical, psychiatric, or social condition that, in the judgement of the investigator, is a contraindication to protocol participation.

Co-enrollment guidelines: Co-enrollment in other interventional trials is restricted, other than enrollment on observational studies. Consideration for co-enrollment in trials evaluating the use of a licensed medication will require the approval of the principal investigator in consultation with the sponsor medical monitor (SMM). Study staff should be notified of co-enrollment on any other protocol as it may require the approval of the principal investigator (in consultation with the SMM).

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:基础科学
  • 分配:非随机化
  • 介入模型:单组作业
  • 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:Heterotypic
Those with their highest titer to a non-DENV2.
The rDEN2delta30-7169 strain is a live attenuated recombinant virus constructed by introducing a 30-nucleotide deletion (delta30) in 3 UTR of the wild type DEN-2 Tonga/74.
实验性的:Homotypic
Those with a DENV2-dominant serotype.
The rDEN2delta30-7169 strain is a live attenuated recombinant virus constructed by introducing a 30-nucleotide deletion (delta30) in 3 UTR of the wild type DEN-2 Tonga/74.
实验性的:Naive
Those with no exposures to flaviviruses
The rDEN2delta30-7169 strain is a live attenuated recombinant virus constructed by introducing a 30-nucleotide deletion (delta30) in 3 UTR of the wild type DEN-2 Tonga/74.

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
The frequency and severity of AEs through day 28 and SAEs through day 180.
大体时间:Through Day 180
Evaluate the safety of the challenge strain in all groups.
Through Day 180
Fold difference between groups in peak viral RNAemia titers on any day from days 2 to 19.
大体时间:Through Day 19
Evaluate viral replication by qRT-PCR and compare the peak replication among groups.
Through Day 19
Fold change in DENV1-4 neutralizing antibody GMTs between days 0 and 28 within each group.
大体时间:Through Day 28
Evaluate the immunogenicity of the challenge by examining the change in antibody titers in each group.
Through Day 28

次要结果测量

结果测量
措施说明
大体时间
Differences in the change in IP-10 signaling between day 0 and days 2 to 19 among groups.
大体时间:Through Day 19
Evaluation of IP-10 over time will allow us to evaluate how prior DENV exposure influences the immune response to viral replication.
Through Day 19
Difference between the bone marrow cellularity at day 5 versus the reference range within each group.
大体时间:At Day 5
Cellularity is measured as the percentage of hematopoietic cells vs. fat in the marrow and will allow us to evaluate whether the marrow is suppressed or proliferative at day 5 in each group.
At Day 5
The magnitude of bone marrow DENV-specific antibody-secreting cells at day 57.
大体时间:At Day 57
The presence of DENV-specific antibody-secreting cells in the bone marrow at day 57 would indicate that long lived immunity has been established and allow us to study the determinants of this immunity.
At Day 57

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。

调查人员

  • 首席研究员:Camila D Odio, M.D.、National Institute of Allergy and Infectious Diseases (NIAID)

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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8月7日

初级完成 (估计的)

2028年11月3日

研究完成 (估计的)

2029年5月3日

研究注册日期

首次提交

2026年7月15日

首先提交符合 QC 标准的

2026年7月15日

首次发布 (实际的)

2026年7月16日

研究记录更新

最后更新发布 (实际的)

2026年9月10日

上次提交的符合 QC 标准的更新

2026年9月9日

最后验证

2026年9月4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)?

是的

IPD 计划说明

All collected IPD may be shared. To protect research participant identities, all direct identifiers will be stripped from datasets. Patient-level variables not needed for interpreting the data will be removed or, where appropriate, anonymized using data masking (hiding data with altered values). Indirect identifiers needed for interpreting the data will be anonymized through generalization (e.g. ranges for age, larger categories for country of birth) or perturbation (slight alteration of the data, e.g. time since last lived in a dengue-endemic region), as appropriate.

IPD 共享时间框架

Scientific data will be made available no later than the time of publication, when possible. We place no restrictions on the length of time data will be made available.

IPD 共享访问标准

IPD used in publications will be de-identified, generalized, and shared as supplemental material, which can be accessed by any person reading the article. De-identified, generalized IPD will also be deposited in ImmPort. Data are available on ImmPort to qualified researchers after a brief registration and approval process. Users must accept a data sharing and access agreement before approval is granted. Genetic data will be deposited in dbGap with only the minimal associated metadata needed for interpretation to reduce any possibility of de-identification. To gain access to data on dbGap, researchers must agree to follow the NIH Genomic Data Sharing (GDS) Policy, and be approved by the NIH Data Access Committee or appropriate Data Access Committee. They must describe the proposed use of the data and ensure all researchers involved in the request will adhere to this project outline. Investigators gain access to the data for one year with the ability to extend to additional years.

IPD 共享支持信息类型

  • 研究方案
  • 树液
  • 国际碳纤维联合会
  • 分析代码
  • 企业社会责任

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

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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