NCT05047692已完成1 期
A Dose Escalation, Multicenter, Open, Phase I Study to Assess the Safety and Immunogenicity of AdCLD-CoV19-1, a COVID-19 Preventive Vaccine in Healthy Volunteers.
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 40
- 试验地点
- 3
- 主要终点
- Incidence of unsolicited AEs
研究概览
简要总结
This is a Phase 1 clinical trial to assess the safety and immunogenicity of AdCLD-CoV19-1 in healthy adults.
详细描述
This is a dose-escalation, multi-center, open-label, Phase 1 clinical trial. We assess the safety of AdCLD-CoV19-1 and immune responses against SARS-CoV-2. DSMB will evaluate safety when events occurred during the whole study period.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Sequential
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 19 Years 至 64 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Able and willing to agree informed consent and aged 19 to 64 years.
- •The BMI index is 18.5 kg/m2 to 30.0 kg/m
- •Able and willing to medically effective contraception during the whole study period.
- •Agreement to refrain from blood donation during the whole study period.
排除标准
- •Anyone deemed infected by COVID-
- •Determined to be a close-contact of SARS-CoV-2 confirmed case or classified to symptomatic patient of COVID-19 prior to vaccination.
- •Clinically significant abnormal ranges of laboratory measurement, ECG, Chest X-ray at screening visit.
- •Positive in HIV, HBV, HCV test at screening visit.
- •Acute fever(≥ 38℃) or suspected infectious disease, symptoms of infectious disease(cough, difficulty breathing, chills, muscle aches, headache, sore throat, loss of smell, or loss of taste, etc.) within 3 days prior to vaccination.
- •Chronic respiratory disease: Asthma, chronic obstructive pulmonary disease, active tuberculosis, latent tuberculosis under treatment.
- •Clinically significant active or any history of disease: Hepatobiliary system, kidney, central or peripheral nervous system (epilepsy, seizure, etc.), endocrine system (uncontrolled diabetes, hyperlipidemia, etc.), cardiovascular system (congestive heart failure, coronary artery disease, myocardial infarction, control Hypertension, etc.), blood tumor, urinary system, mental, musculoskeletal system, immune system (rheumatoid arthritis, systemic lupus erythematosus).
- •Immunosuppressive disease including immunodeficiency disease.
- •Scheduled to undergo any surgery during the whole study period.
- •Healthcare worker who provide medical care to SARS-CoV-2 cases or occupationally in high risk for SARS-CoV-2 exposure during the whole study period.
- •Prisoners or subjects who are compulsorily detained. (involuntary incarceration)
- •History of SARS or MERS.
- •Allergic reaction or hypersensitivity to any ingredient of AdCLD-CoV19-
- •Having hemophilia at risk of causing serious bleeding when injected intramuscularly or receiving anticoagulants.
- •Any history of malignant disease within the past 5 years. History of hypersensitivity to inoculate vaccine such as Guillain-Barre syndrome.
- •History of serious adverse reaction or allergic reaction to inoculate vaccine.
- •Urticaria past 5 years prior to vaccination.
- •History of hereditary angioneurotic edema or acquired angioneurotic edema.
- •History of solid organ or bone marrow transplantation.
- •Suspected or a history of drug or alcohol abuse past 12 month before vaccination.
- •Receipt of vaccine of SARS-CoV, MERS-CoV, SARS-CoV-
- •Receipt of adenovirus vector based vaccine.
- •Chronic use of immunosuppressant or immune modifying drug within 6 months prior to vaccination. (use of inhaled, topical, nasal, and ophthalmic corticosteroids are allowed)
- •Having relied on antipsychotic drugs and narcotic analgesics within 6 months before vaccination or difficult to comply with the clinical trial procedure at the judgment of the investigator.
- •Administered to other investigational product or medical device within 6 months before vaccination.
- •Other vaccination history within 30 days prior to vaccination or being scheduled within 30 days after vaccination.
- •Receipt of immunoglobulin or any blood product within 3 month prior to vaccination.
- •Pregnant(including positive hCG test at screening visit) or breastfeeding female.
- •Those who are directly related to the investigator.
- •Other condition deemed ineligible for the study at the discretion of investigator.
结局指标
主要结局
Incidence of unsolicited AEs
时间窗: Through 28 days post-vaccination
Incidence of solicited adverse events(AEs)
时间窗: Through 7 days post-vaccination
次要结局
- Incidence of serious adverse events(SAEs)(Through 12 months post-vaccination)
- Geometric mean titer(GMT) of neutralization antibody against wild type SARS-CoV-2(4 weeks post-vaccination)
- GMT of S protein specific antibody(2, 4, 26, 52 weeks post-vaccination)
- S protein specific T cell response(2, 4, 26, 52 weeks post-vaccination)
- Incidence of adverse events of special interest(AESIs)(Through 12 months post-vaccination)
- Seroconversion rate(SCR) of neutralization antibody against wild type SARS-CoV-2(4 weeks post-vaccination)
研究者
研究点 (3)
Loading locations...
相似试验
已完成
1 期
Safety and Immunogenicity Study of AdCLD-CoV19: A COVID-19 Preventive Vaccine in Healthy VolunteersCOVID-19NCT04666012Cellid Co., Ltd.150
终止
2 期
Safety and Immunogenicity of COVID-19 Vaccine, AdCLD-CoV19-1COVID-19VaccinesNCT05520970Cellid Co., Ltd.4
已完成
1 期
Safety and Immunogenicity of AdCLD-CoV19-1 OMI as a Booster: A SARS-CoV-2 (COVID-19) Preventive VaccineCOVID-19VaccinesNCT05576623Cellid Co., Ltd.320
Unknown
1 期
Study of Safety and Efficacy of BZ019 in (R/R) Large B-cell LymphomaLarge B-cell LymphomaNCT04250324Shanghai Cell Therapy Group Co.,Ltd21
已完成
1 期
Phase 1 ID93 + GLA-SE Vaccine Trial in Healthy Adult VolunteersPulmonary TuberculosisNCT01599897Access to Advanced Health Institute (AAHI)60