NCT06997653撤回2 期
Open-Label, Phase 2b Clinical Trial to Determine Efficacy, Safety, and Immunogenicity of Inactivated COVID-19 Vaccine (TURKOVAC) Against SARS-CoV-2 in Healthy Pregnant Women
干预措施
相关药物
试验速览
- 阶段
- 2 期
- 状态
- 撤回
- 试验地点
- 1
- 主要终点
- Incidence of Adverse Events
研究概览
简要总结
This study is an open-label and Phase 2b clinical trial of the COVID-19 inactivated TURKOVAC vaccine against SARS-CoV-2 in healthy pregnant women.
详细描述
The main purpose of this study is pregnant women who are at least in the second (13th to 27th weeks) and third (28th to 40th weeks) trimesters, to evaluate of the safety of two doses of TURKOVAC vaccine in who are naive (never vaccinated) and previously vaccinated with two doses of inactivated COVID-19 vaccine.
It is planned to include 30 healthy pregnant subjects between the ages of 18-45 (including both age groups) in the study. After the safety and immunogenicity data obtained from the interim analysis of 30 pregnant female subjects, it will be planned to increase the number of subjects.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Prevention
- 盲法
- None
盲法说明
Open-Label, National, Phase IIB Clinical Trial
入排标准
- 年龄范围
- 18 Years 至 45 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Subjects must meet all of the following inclusion criteria to be eligible for inclusion in the study:
- •Subjects willing and able to give signed informed consent to participate in study,
- •Healthy pregnant female subjects aged 18 - 45 years (including both groups),
- •Females in the second trimester of pregnancy (weeks 13 to 27) and in the third trimester (from week 28 to week 40),
- •Females who were previously vaccinated with two doses of inactivated vaccine also 3 months after their last menstrual period and more than 3 months have passed since they have vaccinated for their last dose,
- •Females without a current positive (real time-polymerase chain reaction (RT-PCR) - based viral RNA (Ribonucleic Acid) detection) or past (serological test or real time-polymerase chain reaction (RT-PCR -based viral RNA (Ribonucleic Acid) detection) positive diagnostic test result for SARS-CoV-2 infection,
- •In the opinion of the investigator, subjects capable and willing to comply with all study requirements,
- •Subjects who agree to comply with all study visits and procedures (who consent to blood and nasopharyngeal swab collection and who can answer automated phone calls from the study center).
排除标准
- •Subjects meeting any of the following criteria will be excluded from the study:
- •Subjects with fever (above 37,8°C) at the time of vaccination and/or up to 72 hours before (subjects may be screened again after acute condition has resolved),
- •Possible history of allergic disease or reaction (e.g. to the active substance) by any component of the study vaccines,
- •Any history of anaphylaxis,
- •Subjects with a medical or obstetric history that puts them at higher risk for maternal or fetal complications (e.g. chronic pregnancy-related disorders, birth defects, or genetic conditions during a previous pregnancy),
- •Subjects with an abnormal uterine cavity shown on hysterosalpingography or hysteroscopy,
- •Subjects with an abnormal pregnancy screening test (e.g. ultrasound fetal abnormalities, maternal blood screening),
- •Subjects with a history of malignancy within 2 years prior to screening (exceptions are squamous, basal cell carcinomas of the skin, carcinomas in situ of the cervix, or malignancy considered treated with minimal risk of recurrence),
- •Females with the presence of hydrosalpinx or endometrial polyp that are not treated surgically,
- •Females with the poor ovarian response (less than 3 mature follicles),
- •Females currently participating in a similar study of another inactive investigational product and currently using this investigational product or who have taken an inactive investigational product in the 28 days before their last menstruation period,
- •In case of clinical necessity, subjects with positive COVID-19 real time-polymerase chain reaction (RT-PCR) test results to be requested from the subjects,
- •Insufficient level of Turkish to perform the informed consent, except where briefing by an independent witness can be provided and is available,
- •Any other significant disease, disorder or finding that could significantly increase the subject's risk for participation in the study, affect the subject's ability to participate in the study, or impair the interpretation of study data; severe and/or uncontrolled cardiovascular disease, respiratory disease, gastrointestinal disease, liver disease, kidney disease, endocrine disorder, and neurological disease (mild/moderate well-controlled comorbidities are permitted),
- •Any confirmed or suspected immunosuppressive or immunodeficiency state; asplenia; recurrent severe infections and use of immunosuppressants (less than ≤14 days) in the last 6 months, excluding topical steroids or short-term oral steroids,
- •History of bleeding disorder (e.g. factor deficiency, coagulopathy or platelet disorder), or prior history of significant bleeding or bruising following intramuscular injections or venipuncture,
- •Continued use of anticoagulants such as coumarins and related anticoagulants (e.g. warfarin) or new oral anticoagulants (e.g. apixaban, rivaroxaban, dabigatran and edoxaban),
- •Subjects with cerebral venous sinus thrombosis, antiphospholipid syndrome, or a history of heparin-induced thrombocytopenia and thrombosis (HITT or HIT type 2),
- •Suspected or known current alcohol or drug addiction,
- •History of active or previous autoimmune neurological disorders (e.g. multiple sclerosis, Guillain-Barre syndrome, transverse myelitis) (Lumbar palsy will not be an exclusion criterion),
- •Subjects with severe renal impairment or liver failure,
- •Acute respiratory disease (moderate or severe illness with or without fever). (Subjects may be screened again after acute condition has resolved).
研究组 & 干预措施
TURKOVAC
Experimental
TURKOVAC-Dollvet vaccines produced by Dollvet Veterinary Vaccine Pharmaceutical Biological Substance Production Industry Co., Ltd.
干预措施: TURKOVAC (Biological)
结局指标
主要结局
Incidence of Adverse Events
时间窗: Incidence of adverse events throughout the entire study from first and second dose vaccinations.
Incidence of obstetric, fetal, and neonatal adverse events of TURKOVAC vaccine.
次要结局
- Neutralizing Antibodies and Pseudo-Neutralizing Antibodies(On days 0, 28±2 (for all subjects) 48±5, 84±5 ve 168±10 (for 50% of all subjects))
- SARS-CoV2 anti-spike protein immunoglobulin G(On days 0, 28±2 (for all subjects) 48±5, 84±5 ve 168±10 (for 50% of all subjects))
- T-Cell(On the 28th day)
- Protection Rate of TURKOVAC(24 hours (subjects with at least 1 symptom within 24 hours) and at least 14 days after the TURKOVAC vaccination dose.)
- The antibody Level in the Cord Blood(Between Visit 0 (-1 or 0. day) Visit 4 (168 day ±10) (At the time of birth))
- Antibody Persistence(6 months and 12 months after vaccination.)
- Incidence of Adverse Reactions(7 to 14 days after vaccination.)
- Incidence of Serious Adverse Events (SAE)(Up to day 365 after vaccination.)
研究者
研究点 (1)
Loading locations...
相似试验
Unknown
4 期
Clinical Trial of Inactivated SARS-CoV-2 Vaccine for Prevention of COVID-19 in Healthy AdultsCOVID-19NCT04962308Sinovac Research and Development Co., Ltd.1,400
进行中（未招募）
2 期
ABNCoV2 Vaccine in SARS-CoV-2 (COVID-19) Seronegative and Seropositive Adult SubjectsCOVID-19 DiseaseNCT05077267Bavarian Nordic197
撤回
2 期
Immunogenicity and Safety Study of the 3rd Booster Dose Using the High or Medium Dose of Inactivated Vaccine in Healthy Adults in in Hong KongCOVID-19NCT05254236Sinovac Research and Development Co., Ltd.
终止
2 期
TTAC-0001 Phase II Trial With Recurrent Glioblastoma Progressed on BevacizumabRecurrent GlioblastomaNCT03856099PharmAbcine19
已完成
不适用
Standard Antiretroviral v. Multi-class Therapy in Acutely HIV-1 Infected Antiretroviral-Naïve Subjects (ADARC 2007-01)HIV InfectionsNCT00525733Rockefeller University40