Resumen

The purpose of this study is to assess pregnancy outcomes, and maternal, as well as neonatal events of interest in healthy pregnant women and their new-borns. The study will also determine incidence of lower respiratory tract illness (LRTI) caused by respiratory syncytial virus (RSV) in the new-borns during their first year of life.

Elegibilidad

Edad mínima: 18 YearsEdad máxima: 40 YearsSexo: ALL

Criterios de inclusión

Healthy pregnant women 18-45years of age who are ≥ 24 0/7 weeks GA at screening and ≤ 27 6/7 weeks GA at Visit 1, as established by ultrasound examination and/or last menstrual period (LMP) date
Women with pre-pregnancy body mass index (BMI) ≥18.5 and ≤ 39.9 kg/m2.
Women whose pregnancy is considered low risk, based on medical history, obstetric history, and clinical findings during the current pregnancy
Women who had no significant findings (such as abnormal fetal morphology, amniotic fluid levels, placenta, or umbilical cord) observed during a Level 2 ultrasound (fetal morphology assessment).
Human Immunodeficiency Virus (HIV) uninfected women who have been tested within the past year and have documented HIV negative test results.
Individuals who give written or witnessed/thumb printed informed consent after the study has been explained according to local regulatory requirements.
The informed consent given at screening should either include consent for both the mother's participation and participation of the infant after the infant's birth (if consistent with local regulations/guidelines), or consent for the mother's participation and expressed willingness to consider permitting the infant to take part after the infant has been born (if local regulations/guidelines require parent(s) to provide an additional informed consent after the infant's birth).
Both mother and father should consent if local regulations/guidelines require it.
Individuals who consent to have cord blood collected at delivery for the purpose of the study;
Individuals who plan to reside in the study area for at least one year after delivery.
Individuals who are in good health as determined by the outcome of medical history, physical examination and clinical judgment of the investigator;
Individuals who, in the opinion of the investigator can and will comprehend and comply with all study procedures
Infants who were in utero at the time maternal (and paternal, if required) informed consent was given, and who are live-born.
If local law requires it: Written or witnessed/thumb printed informed consent for study participation of the infant obtained from parent(s)/Legally Accepted Representative \[LAR(s)\] within 21 days of birth.

Criterios de exclusión

Child in care
Individuals pregnant with a fetus with a confirmed or suspected major congenital anomaly at the time of enrolment.
Individuals determined to have one of the following conditions associated with increased risk for a serious obstetrical complication
Gestational hypertension;
Gestational diabetes uncontrolled by diet and exercise;
Pre-eclampsia or eclampsia;
Multiple pregnancy;
Intrauterine growth restriction;
Placenta previa;
Polyhydramnios;
Oligohydramnios;
Individuals determined to have (during the current pregnancy) one of the following infections or conditions associated with risk of adverse outcome:
Known or suspected:
Syphilis infection,
Parvovirus B19,
Rubella infection,
primary herpes simplex infection,
primary cytomegalovirus infection,
varicella infection,
Zika infection,
Active tuberculosis infection,
Incompetent cervix or cerclage
Individuals who have any underlying condition or infection that would predispose them to increased risk for a serious obstetrical complication that is not mentioned above
Individuals who have behavioural or cognitive impairment or psychiatric disease that, in the opinion of the investigator, could interfere with the subject's ability to participate in the study;
Individuals who have known or suspected impairment of the immune system, an active autoimmune disorder that is not well-controlled, or who are receiving systemic immunosuppressive therapy;
Individuals participating in any concurrent clinical trial during the current pregnancy;

Intervenciones

procedure

Blood sample collection

Venous blood samples will be collected from the maternal subjects at Day 1 and Day 56 of the study and at delivery.

procedure

Cord blood sample collection

Collection of cord blood samples from maternal subjects will occur, at delivery

other

Maternal Diary Card

Completion of Diary Card about health by pregnant woman/ mother, from enrolment through week 6 post delivery.

procedure

Nasal Swab collection

Collection of nasal swabs from infants with potential LRTIs, from birth to 12 months of age.

other

Infant Diary Card

Completion of Diary Card about health of infant from birth to 12 months of age.

A Prospective Epidemiological Study of Pregnancy Outcomes and of Events of Interest in Pregnant Women, Neonates and Infants (PEPNI)

Resumen

Elegibilidad

Criterios de inclusión

Criterios de exclusión

Intervenciones

Blood sample collection

Cord blood sample collection

Maternal Diary Card

Nasal Swab collection

Infant Diary Card

Ubicaciones

GSK Investigational Site

GSK Investigational Site

GSK Investigational Site

GSK Investigational Site

GSK Investigational Site

GSK Investigational Site

Patrocinadores