A Follow-up Study to Describe the Safety of Study Participants Who Received RSVPreF3 Maternal Vaccination (Any Dose) or Controls From Previous RSV MAT Studies During Any Pregnancy Conceived Post Vaccination/Control
Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
GlaxoSmithKline
Age
9–49
Sex
FEMALE
Healthy volunteers
Accepted
You may be eligible if
Retrospective cohort
Adult/Adolescent Participant:
Adult/Adolescent study participant from any of the prior RSV MAT studies who have either received RSV MAT vaccine or control (placebo, Tdap or influenza vaccine).
Study participant:
* who has reached 2 years+2 months post vaccine/control prior to/at enrolment or
* who has not reached 2 years+2 months post vaccine/control prior to/at enrolment but is a Woman of Nonchildbearing Potential (WONCBP) at study enrolment, or recipient of bilateral tubal ligation prior to study enrolment.
Study participant with any pregnancy conceived post vaccination/control, that has reached Day 42 post-delivery prior to/at enrollment.
Provide signed and dated informed consent form.
Be willing to comply with all study requirements and be available for the duration of the study.
Infant Participant:
Participant live born as the result of a pregnancy followed in an adult/adolescent participant in this study.
Signed and dated informed consent form obtained from the participant's parent(s)/LAR(s) prior to performance of any study-specific procedure.
Prospective cohort
Adult/Adolescent Participant:
Adult/adolescent study participant from any of the prior RSV MAT studies who have either received RSV MAT vaccine or control (placebo, Tdap or influenza vaccine).
Study participant:
* who has not reached 2 years+2 months post vaccine/control prior to/at enrollment or
* who has reached at least 2 years+2 months post vaccine/control but has an ongoing pregnancy (prior to Day 42 post-delivery) at enrollment. Participants who have reached 2 years post-vaccine/control before enrollment but are pregnant at enrollment will be enrolled and followed until Day 42 post-delivery for the pregnancy ongoing at enrollment.
Female participants of childbearing potential.
Provide signed and dated informed consent form.
Be willing to comply with all study procedures and be available for the duration of the study.
Infant Participant:
Participant live born as the result of a pregnancy followed in an adolescent/adult participant in this study.
Participant's parent(s)/LAR(s), in the opinion of the investigator, can and will comply with the requirements of the protocol.
Signed and dated informed consent form obtained from the participant's parent(s)/LAR(s) prior to performance of any study-specific procedure.
You may not be if
Adult/adolescent participant otherwise eligible for the prospective cohort:
Woman of Nonchildbearing Potential (WONCBP) at study enrollment, or recipient of bilateral tubal ligation prior to study enrollment, if she has not conceived a pregnancy post-vaccine/control and does not plan to use any additional measures to attempt to conceive a pregnancy (e.g., sterilization reversal or IVF).
Infant participant:
Child in care.
Clareo Health | A Follow-up Study to Describe the Safety of Study Participants Who Received RSVPreF3 Maternal Vaccination (Any Dose) or Controls From Previous RSV MAT Studies During Any Pregnancy Conceived Post Vaccination/Control
