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A Safety, Reactogenicity and Immunogenicity Trial of RVX-sCPD9 Booster Intranasal COVID-19 Vaccine

A Phase 1, Open-Label, Safety, Reactogenicity, and Immunogenicity Trial of RVX-sCPD9, a Live-Attenuated SARS-CoV-2, as a Booster Vaccine, Via the Intranasal Route in Previously Vaccinated Adults

This phase 1 clinical trial will evaluate the safety, reactogenicity, and immunogenicity of RVX-sCPD9, given Intranasally (IN), as a booster dose to previously vaccinated healthy adults. The study is designed as a non-randomized, open-label, dose-escalation clinical trial evaluating four dose levels of RVX-sCPD9 administered IN (10^2, 10^3, 10^4, 5 x 10^4 FFU). A sample size of 80 participants (20 participants in each cohort).

The primary objective is to evaluate the safety and reactogenicity of a single IN administration of 4 ascending dosages of RVX-sCPD9 in previously vaccinated healthy adults.

研究概览

地位

尚未招聘

条件

干预/治疗

详细说明

This Phase 1 clinical trial will evaluate the safety, reactogenicity, and immunogenicity of RVX-sCPD9 administered as an intranasal (IN) booster in previously vaccinated healthy adults. The study is designed as a non-randomized, open-label, dose-escalation trial assessing four dose levels of RVX-sCPD9 (10^2, 10^3, 10^4, and 5 × 10^4 FFU) delivered intranasally. A total of 80 participants will be enrolled, with 20 participants in each cohort.

Eligibility will be determined at screening and confirmed again on Day 1 prior to study product administration. Participants will be healthy adults aged 18 to 64 years, regardless of prior SARS-CoV-2 infection status, who have completed a primary COVID-19 vaccination series and received at least one booster dose, with the most recent vaccination administered at least 16 weeks prior to study vaccination.

Each participant will receive a single dose of RVX-sCPD9 administered intranasally using a nasal atomization device, delivering 0.25 mL per nostril. Three sentinel participants under 50 years of age will be enrolled initially, followed by enrollment of the remaining participants.

The total study duration is approximately 1.5 years, with each participant involved for up to 7 months. The primary objective is to evaluate the safety and reactogenicity of a single intranasal administration of 4 ascending dose levels of RVX-sCPD9 in previously vaccinated healthy adults. Secondary objectives include include evaluating systemic anti-Spike humoral immune responses and evaluating nasal mucosal Immunoglobulin A (IgA) and Immunoglobulin G (IgG) responses after intranasal administration of RVX-sCPD9.

研究类型

介入性

注册 (估计的)

80

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

    • New York
      • New York、New York、美国、10016-6402
        • New York University School of Medicine - Langone Medical Center - Vaccine Center
        • 接触:
    • North Carolina
      • Durham、North Carolina、美国、27703
        • Duke Vaccine and Trials Unit
        • 接触:
    • Ohio
      • Cincinnati、Ohio、美国、45229-3039
        • Cincinnati Children's Hospital Medical Center Vaccine Research Center
        • 接触:
    • Texas
      • Houston、Texas、美国、77030-3411
        • Baylor College of Medicine
        • 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:

  1. Provides written informed consent before initiation of any study procedures.
  2. Able to understand and agree to comply with planned study procedures and be available for all study visits.
  3. Non-pregnant adults, 18 through 64 years of age at the time of study product administration.
  4. Participants of childbearing potential* must agree to use or have practiced true abstinence** or use at least one acceptable primary form of contraception***.

    *These criteria apply to females who are in a heterosexual relationship who are of childbearing potential. Not of childbearing potential include post-menopausal females (defined as having a history of amenorrhea for at least one year) or a documented status as being surgically sterile (hysterectomy, bilateral oophorectomy, or tubal ligation/salpingectomy).

    **True abstinence is 100% of the time, no sexual intercourse (penis enters the vagina). Periodic abstinence (e.g., calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are not acceptable methods.

    ***Acceptable forms of primary contraception include a monogamous relationship with a vasectomized partner who has been vasectomized for 180 days or more before the participant's study product administration, intrauterine devices, birth control pills, and injectable/implantable/insertable/transdermal hormonal birth control products. Must have used at least one acceptable primary form of contraception for at least 30 days before study product administration and agree to continue at least one acceptable primary form of contraception through 60 days after study product administration.

  5. Participants of childbearing potential must have a negative urine pregnancy test at screening and within 24 hours before study product administration.
  6. In general good health*.

    *As determined by medical history and physical examination, including vital signs, to evaluate acute or ongoing chronic medical diagnoses/conditions that have been present for at least 90 days, which would affect the assessment of the safety of participants. Chronic medical diagnoses/ conditions should be stable for the last 30 days (i.e., no hospitalizations, ER, or urgent care for the condition). This includes no change in chronic prescription medication, dose, or frequency due to deterioration of the chronic medical diagnosis/condition 30 days before the study product administration. Any prescription change due to a change of health care provider, insurance company, etc., or done for financial reasons and in the same class of medication will not be considered a deviation of this inclusion criterion. Participants may be on chronic or as-needed (prn) medications if, in the opinion of the participating site PI or appropriate sub-investigator, they pose no additional risk to participant safety or assessment of reactogenicity and immunogenicity.

  7. Receipt of a complete primary authorized or approved COVID-19 vaccine series and at least one booster* with the last vaccination at least 16 weeks before study product administration.

    *Booster may be either homologous or heterologous to the primary vaccine series. It must be an FDA-authorized/licensed vaccine, though doses may have been received during a clinical trial (see MOP for further details).

  8. Clinical screening laboratory evaluations are within normal reference ranges or grade 1 with no clinical significance (NCS) per the investigator's discretion*.

    *Laboratory evaluations include White Blood Cells [WBCs] with differential, hemoglobin [Hgb], platelets [PLTs], Alanine Transaminase [ALT], Aspartate Transaminase [AST], Creatinine [Cr], Alkaline Phosphatase [ALP], and Total Bilirubin [T. Bili]). Clinical laboratory evaluations that are below the site reference range, but not graded by the toxicology table, are not exclusionary unless deemed clinically significant by an investigator.

  9. Must agree to have samples stored for secondary research.

Exclusion Criteria:

  1. Positive SARS-CoV-2 PCR at screening.
  2. Abnormal vital signs (Grade 1 or higher)*.

    *Grade 1 or higher is equivalent to: Systolic blood pressure (SBP) >/= 141 mmHg or </= 89 mmHg. Diastolic blood pressure (DBP) >/= 91 mmHg. Heart rate (HR) is >/= 101 beats per minute or </= 54 beats per minute. Oral temperature >/= 38.0 degrees Celsius (100.4 degrees Fahrenheit).

  3. Self-reported or medically documented SARS-CoV-2 infection (regardless of whether symptomatic or asymptomatic) within 16 weeks prior to study product administration.
  4. Participant who is pregnant or breastfeeding.
  5. Blood or plasma donation within 4 weeks before study product administration.
  6. Receipt of antibody or blood-derived products within 90 days before study product administration.
  7. Any self-reported or documented significant medical or psychiatric diseases* or any other condition that, in the opinion of the site PI or appropriate sub-investigator, precludes study participation.

    *Significant medical or psychiatric conditions include but are not limited to drug or alcohol abuse within 6 months of enrollment, significant kidney disease, liver disease, ongoing malignancy, or recent diagnosis of malignancy in the last five years, excluding treated basal and squamous cell carcinoma of the skin and cervical carcinoma in situ, which are allowed.

  8. Neurological conditions*.

    *Including history of Bell's palsy, history of four or more migraine headaches in the past 12 months that interfered with normal daily activity or any migraine headache in the past 5 years that required emergency or inpatient medical care, epilepsy, seizures in the last 5 years, encephalopathy, focal neurologic deficits, Guillain-Barré syndrome, encephalomyelitis, transverse myelitis, stroke or transient ischemic attack, multiple sclerosis, Parkinson's disease, amyotrophic lateral sclerosis, Creutzfeldt-Jakob disease, or Alzheimer's disease.

  9. History of significant respiratory disease currently requiring daily medications, history of asthma in the past 5 years, or any treatment of respiratory disease exacerbations in the last 5 years.
  10. History of cardiovascular disease (e.g., congestive heart failure, cardiomyopathy, ischemic heart disease), including any history of myocarditis, pericarditis, or uncontrolled cardiac arrhythmia.
  11. Any autoimmune disease, including hypothyroidism, without a defined non-autoimmune cause.
  12. Has an acute illness determined by the site PI or appropriate sub-investigator within 72 hours before study product administration*.

    *An acute illness that is nearly resolved with only minor residual symptoms remaining is allowable if, in the opinion of the participating site PI or appropriate sub-investigator, the residual symptoms will not interfere with the ability to assess safety parameters as required by the protocol.

  13. Has a positive test result for hepatitis B surface antigen, hepatitis C virus RNA (by reflex testing), or human immunodeficiency virus (HIV) antigen/antibody test at screening.
  14. Has any confirmed or suspected immunosuppressive or immunodeficient state such as asplenia, recurrent severe infections, and chronic* immunosuppressant medication within the past 6 months**.

    *Chronic means more than 14 continuous days.

    **Ophthalmic and topical steroids are allowed. See exclusion 19 for intranasal steroids.

  15. Has received any investigational study product within 60 days, or 5 half-lives, whichever is longer, before study product administration or is planning to receive one during the study.
  16. Has a history of hypersensitivity or severe allergic reaction* to any previous licensed or unlicensed vaccines or the candidate study product components**.

    *(e.g., anaphylaxis, generalized urticaria, angioedema, other significant reaction).

    • See IB for study product formulation.
  17. Received or plans to receive licensed inactivated/subunit vaccine within 14 days of study product administration or live vaccine within 28 days of study product administration.
  18. Plan to receive a COVID-19 booster vaccine within the 180 days following study product administration.
  19. Regular use of intranasal medications, including steroids, and sinus rinsing treatments*.

    *Participants must have had no intranasal medication use for 30 days before study product administration and do not plan to use intranasal medications for 30 days after study product administration for medications other than steroids and for 6 months after study product administration for intranasal steroids (including over the counter (OTC) fluticasone). Participants should not use nasal irrigation or sinus rinsing treatments (e.g., Neti pots or saline washes) for 28 days after the study product administration and 7 days before study visits for the duration of the trial.

  20. Use of illicit intranasal drugs in the 5 years before study product administration or plans to use during the study.
  21. Current smoker (including cigarettes, marijuana, and vaping) or smoking within the prior 3 months.
  22. Planned international travel between study product administration and Day 29 visit.
  23. Any significant nasal or upper airway disease*.

    *Including, but not limited to, being prone to epistaxis, has a history of inflammatory rhinitis (including allergic rhinitis) that requires daily medications, cochlear implants, head/neck radiation history, anosmia/dysosmia, and certain ear, nose and throat (ENT) conditions, including major anatomic nasopharyngeal abnormality or sinus polyp disease due to chronic sinusitis.

  24. Living with a person who has a condition that predisposes to high risk of severe COVID-19 or >/=2 conditions that predisposes to increased risk of COVID-19 per IDSA guidelines.
  25. Healthcare workers with patient-facing responsibilities.
  26. Resides in or works in a nursing home or other skilled nursing facility.
  27. Allergy or contraindications to nirmatrelvir, ritonavir, or remdesivir.

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:预防
  • 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:Arm 1
Healthy adults will receive a single dose of 1x10^2 FFU RVX-sCPD9 vaccine. It will be administered intranasally through a nasal atomization device with a spray divider to provide 0.25mL in each nostril. 3 sentinel participants, under 50 years of age, will be enrolled first and then the reminder. N= 20
RVX-sCPD9 is a live-attenuated SARS-CoV-2 vaccine candidate engineered from the ancestral B.1 strain for intranasal administration to prevent coronavirus disease 2019 (COVID-19) and reduce viral transmission. The vaccine was generated through two complementary attenuation strategies: a codon-pair-deoptimization of the viral genome that reduced viral fitness while preserving protein amino acid sequence, and a deletion of the spike furin cleavage site (FCS), a modification known to prevent horizontal transmission and further attenuate pathogenicity.
实验性的:Arm 2
Healthy adults will receive a single dose of 1x10^3 FFU RVX-sCPD9 vaccine. It will be administered intranasally through a nasal atomization device with a spray divider to provide 0.25mL in each nostril. 3 sentinel participants, under 50 years of age, will be enrolled first and then the reminder. N= 20
RVX-sCPD9 is a live-attenuated SARS-CoV-2 vaccine candidate engineered from the ancestral B.1 strain for intranasal administration to prevent coronavirus disease 2019 (COVID-19) and reduce viral transmission. The vaccine was generated through two complementary attenuation strategies: a codon-pair-deoptimization of the viral genome that reduced viral fitness while preserving protein amino acid sequence, and a deletion of the spike furin cleavage site (FCS), a modification known to prevent horizontal transmission and further attenuate pathogenicity.
实验性的:Arm 3
Healthy adults will receive a single dose of 1x10^4 FFU RVX-sCPD9 vaccine. It will be administered intranasally through a nasal atomization device with a spray divider to provide 0.25mL in each nostril. 3 sentinel participants, under 50 years of age, will be enrolled first and then the reminder. N= 20
RVX-sCPD9 is a live-attenuated SARS-CoV-2 vaccine candidate engineered from the ancestral B.1 strain for intranasal administration to prevent coronavirus disease 2019 (COVID-19) and reduce viral transmission. The vaccine was generated through two complementary attenuation strategies: a codon-pair-deoptimization of the viral genome that reduced viral fitness while preserving protein amino acid sequence, and a deletion of the spike furin cleavage site (FCS), a modification known to prevent horizontal transmission and further attenuate pathogenicity.
实验性的:Arm 4
Healthy adults will receive a single dose of 5x10^4 FFU RVX-sCPD9 vaccine. It will be administered intranasally through a nasal atomization device with a spray divider to provide 0.25mL in each nostril. 3 sentinel participants, under 50 years of age, will be enrolled first and then the reminder. N= 20
RVX-sCPD9 is a live-attenuated SARS-CoV-2 vaccine candidate engineered from the ancestral B.1 strain for intranasal administration to prevent coronavirus disease 2019 (COVID-19) and reduce viral transmission. The vaccine was generated through two complementary attenuation strategies: a codon-pair-deoptimization of the viral genome that reduced viral fitness while preserving protein amino acid sequence, and a deletion of the spike furin cleavage site (FCS), a modification known to prevent horizontal transmission and further attenuate pathogenicity.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Occurrence of abnormal clinical safety laboratory adverse events (AEs)
大体时间:Through Day 15
Through Day 15
Occurrence of Adverse Events of Special Interest (AESIs)
大体时间:Through Day 181
Through Day 181
Occurrence of Medically-Attended Adverse Events (MAAEs)
大体时间:Through Day 181
Through Day 181
Occurrence of solicited local adverse events (AEs)
大体时间:Through Day 15
Through Day 15
Occurrence of solicited systemic adverse events (AEs)
大体时间:Through Day 15
Through Day 15
Occurrence of unsolicited adverse events (AEs)
大体时间:Through Day 29
Through Day 29
Occurrence of New-Onset Chronic Medical Conditions (NOCMCs)
大体时间:Through Day 181
Through Day 181
Occurrence of Serious Adverse Events (SAEs)
大体时间:Through Day 181
Through Day 181

次要结果测量

结果测量
大体时间
Nasal mucosal Immunoglobulin A (IgA) anti-S binding antibodies
大体时间:Through Day 181
Through Day 181
Nasal mucosal Immunoglobulin G (IgG) anti-S binding antibodies
大体时间:Through Day 181
Through Day 181
Serum anti-S binding Immunoglobulin A (IgA) antibodies
大体时间:Through Day 181
Through Day 181
Serum anti-S binding Immunoglobulin G (IgG) antibodies
大体时间:Through Day 181
Through Day 181
Serum anti-S neutralizing antibodies
大体时间:Through Day 181
Through Day 181

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 (估计的)

2026年9月5日

初级完成 (估计的)

2027年11月15日

研究完成 (估计的)

2027年11月15日

研究注册日期

首次提交

2026年7月9日

首先提交符合 QC 标准的

2026年7月9日

首次发布 (实际的)

2026年7月14日

研究记录更新

最后更新发布 (实际的)

2026年9月18日

上次提交的符合 QC 标准的更新

2026年9月17日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

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

在美国制造并从美国出口的产品

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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