Phase 1 Safety Evaluation of PfSPZ Vaccine in Pregnant Women in Mali (MalVIP1)
试验速览
- 阶段
- 1 期
- 状态
- 撤回
- 入组人数
- 400
- 试验地点
- 1
- 主要终点
- Safety using a composite of adverse maternal and birth outcomes
研究概览
简要总结
Background:
Malaria is a disease that affects many people in Africa. It is caused by germs carried by some mosquitoes. A person bitten by an infected mosquito will get malaria. Most malaria infections cause only mild symptoms or none at all, but sometimes the disease can be deadly. Malaria can also harm pregnant women. They may lose their pregnancies or deliver too early, and the mother and newborn may die. An experimental malaria vaccine (PfSPZ) has shown some protection against malaria infection. It is not yet known if PfSPZ is safe for pregnant women.
Objective:
To test the PfSPZ vaccine in pregnant women.
Eligibility:
Healthy women aged 18 to 34 years at 14 to 32 weeks gestation with 1 fetus.
Design:
The study will be in Mali. Participants will have about 40 clinic visits over 20 months.
They will be screened. They will have an ultrasound exam and a test of their heart function. They will have blood and urine tests.
Participants will receive an injection through a needle into a vein on 3 visits over 1 month. Some will receive the PfSPZ vaccine; others will be injected with salt water. They will not know which injection they are getting.
After the last injection, participants will visit the clinic every 2 weeks. They will have blood tests at each visit.
After giving birth, participants and their infants will visit the clinic every 2 weeks for 4 months; then they will have visits each month until the infant is 1 year old. The infant will be examined and will have blood tests at each visit.
详细描述
Study Description:
A randomized double blind, placebo-controlled study to assess the safety, tolerability, immunogenicity and protective efficacy of a 1, 8, 29-day regimen of 9x105 PfSPZ of PfSPZ Vaccine or placebo (normal saline) in healthy pregnant women and their fetus/newborn. The first immunization is to be administered at 16 0/7 to 32 6/7 weeks of gestation and targeted to be completed prior to delivery. Offspring and post-partum women will be followed for 12 months post-delivery.
The study is composed of two cohorts (3rd trimester: Arms 1A, 2A, 2nd trimester: Arms 1B, 2B) with two arms (PfSPZ Vaccine, normal saline placebo) and associated offspring. Enrollment and vaccinations will be staggered for safety with only third trimester women (n=30; based on guidance provided by regulatory bodies) enrolling first in two separate subsets (n=10 [5 PfSPZ Vaccine/5 normal saline], n=20 [10 PfSPZ Vaccine/10 normal saline]) and receiving all three doses of vaccine in a staggered manner and undergoing safety reviews prior to further enrollments. Third trimester enrollment in this staggered manner is to account for any significant events occurring immediately post initial vaccinations with the smaller first subset of women (n=10; DSMB review). After all third trimester pregnancy outcomes are reviewed (by DSMB, FDA, Sponsor, EC/IRB), an additional cohort of women in their second trimester will be vaccinated in two separate subsets (n=10 [5 PfSPZ Vaccine/5 normal saline], n=20 [10 PfSPZ Vaccine/10 normal saline]) separated by at least six weeks. A longer time period of review will be conducted during the 2nd trimester out of additional safety measures to ensure no significant events of concern occur post receipt of a full vaccination series (n=10; DSMB review) before proceeding to the last subset of women (n=20).
Arm 1 (9x10^5 PfSPZ Vaccine): (n = 30) pregnant women will receive three doses of PfSPZ Vaccine (9x10^5 PfSPZ) via direct venous inoculation (DVI) at 1, 8, 29 days
- Arm 1A: (n=15) women 28 0/7 to 32 6/7 WGA (third trimester) at time of first vaccination
- Arm 1B: (n=15) women 16 0/7 to 27 6/7 WGA (second trimester) at time of first vaccination
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- — 至 34 Years（Child, Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •INCLUSION CRITERIA:
- •In order to be eligible to participate in this study, an individual must meet all of the following
- •Willing and able to provide consent for study participation for herself and for her infant prior to initiation of any study procedures
- •Stated willingness to comply with all study procedures and availability of both mother and offspring for the duration of the study
- •Healthy, pregnant women 18-34 years of age (inclusive)
- •Singleton pregnancy (confirmed by ultrasound)
- •Gestational weeks of pregnancy, confirmed by best obstetrical estimate, at minimum of 16 weeks 0 days and a maximum of 32 weeks 6 days of gestation at the time of the first dose of PfSPZ Vaccine and minimum 14 weeks 0 days and maximum of 32 week 0 days of gestation at the time of the first dose of IPTp
- •-Note: women may be screened prior to 16 0/7 weeks gestation for dating of pregnancy
- •Documented first, second, or third trimester ultrasound with singleton gestation and no significant fetal anomalies or other abnormalities
- •Able to provide proof of identity to the satisfaction of the study clinician completing the enrollment process
- •Identified antenatal care provider outside of the study team
- •In good general health as evidenced by medical history
- •Willing to have blood samples stored for future research
排除标准
- •An individual who meets any of the following criteria will be excluded from participation in this
- •Medical, behavioral, cognitive, or psychiatric disease that in the opinion of the investigator affects the ability of the participant to understand and comply with the study protocol
- •Hemoglobin (Hgb), WBC, absolute neutrophils, and platelets outside the local laboratory defined limits of normal per trimester and >= Grade 2 (participants may be included at the investigator s discretion for not clinically significant abnormal values)
- •Alanine transaminase (ALT) or creatinine (Cr) level above the local laboratory-defined (per trimester) upper limit of normal and >= Grade 2 (participants may be included at the investigator s discretion for not clinically significant abnormal values)
- •Infected with HIV, hepatitis B, hepatitis C, syphilis, toxoplasmosis, rubella as documented by testing at screening
- •Sickle cell disease (HbSS or HbSC) or sickle trait (HbAS) by testing at screening
- •Clinically significant abnormal ECG such as abnormal QTc
- •History of receipt of the following:
- •Investigational malaria vaccine in the last 5 years
- •Immunoglobulins and/or blood products within 6 months of enrollment
- •Investigational product within 3 months of enrollment
- •Chronic (>=14 days) oral or IV corticosteroids (excluding topical or nasal) at immunosuppressive doses (i.e., prednisone >=20 mg/day or equivalent) or immunosuppressive drugs within 30 days of enrollment
- •Live vaccine within 30 days of enrollment
- •Non-live vaccine within 14 days of enrollment or planned receipt of a killed vaccine within 14 days of scheduled vaccination
- •Known medical problems:
- •Pre-existing autoimmune or antibody-mediated diseases (e.g. systemic lupus erythematosus,
- •rheumatoid arthritis, multiple sclerosis, Sj(SqrRoot)(Delta)gren s syndrome, or autoimmune thrombocytopenia)
- •Severe asthma (defined as asthma that is unstable or required emergent care, urgent care, hospitalization, or intubation during the past two years, or that has required the use of oral or parenteral corticosteroids at any time during the past two years)
- •Immunodeficiency disorder
- •Asplenia or functional asplenia
- •Diabetes (inclusive of Type 1, 2, or gestational)
- •Deep venous thrombosis or thromboembolic event (current or prior history)
- •Seizures (exception is simple febrile seizures during childhood)
- •History of prior uterine surgery
- •Evidence of clinically significant neurologic, cardiac, pulmonary, hepatic, endocrine, rheumatologic, autoimmune, hematological, oncologic, or renal disease by history, physical examination, and/or laboratory studies
- •Medical, occupational, or family problems as a result of alcohol or illicit drug use during the past 12 months
- •History of a severe allergic reaction or anaphylaxis following previous vaccinations or medications
- •Known allergies or other contraindications against: PfSPZ Vaccine, human serum albumin
- •Positive screening testing or diagnostics for entities (pathogens, diseases) deleterious to pregnancy
- •Nullipara (P<1) or grandimultipara (P>=5)
- •Body mass index (BMI) at enrollment >=30
- •Prior or current pregnancy history of:
- •2 or more spontaneous miscarriages
- •Any unexplained stillbirths
- •Any unexplained neonatal deaths
- •Infant with major congenital anomalies
- •Infant with known genetic disorder
- •Preterm deliveries (< 37 0/7 WGA)
- •Severe pre-eclampsia and/or eclampsia
- •Gestational hypertension
- •Gestational diabetes
- •Red blood cell isoimmunization
- •Cervical insufficiency or incompetent cervix
- •Polyhydramnios or oligohydramnios
- •Premature contractions or preterm labor
- •Bleeding through gestation
- •Known intrauterine fetal growth restriction
- •Use of anti-coagulants during pregnancy
- •Receipt of progesterone during current pregnancy
- •Prior Cesarean section
- 另有 2 项未显示
研究组 & 干预措施
Arm 2
(n = 30) pregnant women will receive normal saline via DVI at 1, 8, 29 days
干预措施: Normal Saline (Drug)
Arm 1
(n = 30) pregnant women will receive three doses of PfSPZ Vaccine (9x10^5 PfSPZ) via direct venous inoculation (DVI) at 1, 8, 29 days
干预措施: PfSPZ Vaccine (Biological)
Arm 1
(n = 30) pregnant women will receive three doses of PfSPZ Vaccine (9x10^5 PfSPZ) via direct venous inoculation (DVI) at 1, 8, 29 days
干预措施: PfSPZ Diluent (Other)
结局指标
主要结局
Safety using a composite of adverse maternal and birth outcomes
时间窗: One year
Composite endpoint of adverse maternal or birth outcomes defined as: preterm birth, miscarriage, stillbirth, early neonatal death, direct maternal death, low birth weight, small for gestational age (counts and proportions)
次要结局
- Safety and tolerability in pregnant women and their fetuses using solicited adverse events (AEs), unsolicited AEs, and laboratory abnormalities(7 and 14 days post injection; 6 months after delivery)