A Study of Spinraza (Nusinersen) Exposure in Pregnant Women With Spinal Muscular Atrophy (SMA) Within Existing SMA Registries
- Conditions
- Muscular Atrophy, Spinal
- Interventions
- Other: No Intervention
- Registration Number
- NCT05789758
- Lead Sponsor
- Biogen
- Brief Summary
The primary objectives of the study are to prospectively evaluate pregnancy complications and outcomes in participants with SMA, birth outcomes and adverse effects in infants born to participants with SMA, who were exposed to nusinersen up to 14 months prior to the first day of their last menstrual period (LMP) before conception, 14.5 months before the date of conception, and/or at any time during their pregnancy. The secondary objective of the study is to evaluate pregnancy outcomes in participants with SMA exposed to nusinersen as compared with participants without SMA who were not exposed to nusinersen (e.g., participants from external, general population comparators).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Female
- Target Recruitment
- 20
- Participant who is currently pregnant (or was pregnant during the relevant exposure window) and enrolled in the United States (US) network of the ISMAR registry, the United Kingdom (UK) Adult SMA REACH, or the Germany, Austria, or Switzerland network of the SMArtCARE registry
- Genetic documentation of spinal muscular atrophy linked to chromosome 5q (5q SMA)
- Documentation that the participant was exposed to nusinersen up to 14 months prior to the first day of their LMP before conception, 14.5 months before conception, and/or at any time during their pregnancy
Key
- Treatment with risdiplam at any time from the first day of their LMP, 2 weeks prior to the date of conception (approximately 5 half-lives), and/or plans to receive treatment with risdiplam during pregnancy
NOTE: Other protocol defined Inclusion/Exclusion criteria may apply
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Nusinersen Treated Participants No Intervention Pregnant participants with SMA who are exposed to nusinersen during the relevant window defined as 14 months prior to the first day of the participant's last menstrual period before conception, 14.5 months before conception and anytime during pregnancy and are enrolled in the registries, International Spinal Muscular Atrophy Registry (ISMAR) and SMArtCARE will be followed prospectively up to 3 months post-delivery, the infants will be followed up to 2 years post-delivery and the available data is collected retrospectively.
- Primary Outcome Measures
Name Time Method Number of Infants Small for Gestational Age Birth Up to 10 years Birth weight will be classified as small for gestational age (\<10th percentile), appropriate (10th-90th percentile), or large (\>90th percentile).
Number of Spontaneous Abortions Up to 10 years Spontaneous abortion is defined as any loss of a fetus due to natural causes at \<20 weeks of gestation.
Number of Fetal Deaths Up to 10 years Fetal deaths include early fetal loss which is fetal death occurring at ≥20 weeks but \<28 weeks of gestation and late fetal loss which is fetal death occurring at ≥28 weeks of gestation.
Number of Maternal Deaths Up to 10 years Maternal deaths during pregnancy, labor, delivery, or up to 12 weeks after delivery will be reported.
Number of Pregnancy Terminations Up to 10 years Pregnancy termination is defined as any induced or voluntary fetal loss during pregnancy.
Number of Live Births Up to 10 years Live births include premature births which is defined as delivery at \<37 weeks of gestation, full term birth which is defined as delivery at ≥37 weeks of gestation.
Number of Major Congenital Malformations (MCMs) Up to 10 years MCMs (interchangeably referred to as congenital malformations, congenital anomalies, and birth defects) are abnormalities in structural development that are medically or cosmetically significant, are present at birth, and persist in postnatal life unless or until repaired.
Number of Neonatal, Perinatal, and Infant Deaths Up to 10 years Neonatal death is defined as death occurring in a newborn prior to 28 days after birth. Perinatal death is defined as death occurring at or after 28 days and prior to 12 weeks after birth. Infant death is defined as death occurring between 12 and 52 weeks after birth, inclusive.
Number of Ectopic and Molar Pregnancies Up to 10 years Ectopic pregnancy is defined as a pregnancy that occurs outside of the uterine cavity. Molar pregnancy is defined as genetically abnormal conceptions characterized by abnormal chorionic villi, trophoblastic hyperplasia, poor fetal development, and an increased risk of malignant disease development.
Number of Infants With Abnormal Postnatal Growth and Development and Neurobehavioral Impairment Up to 10 years Abnormal postnatal growth and development and neurobehavioral impairment in infants up to 24 months of age will be reported.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (10)
St George's University NHS Foundation Trust
🇬🇧London, Greater London, United Kingdom
The Northern Care Alliance NHS Foundation Trust
🇬🇧Salford, Greater Manchester, United Kingdom
University Hospital Southampton NHS Foundation Trust
🇬🇧Southampton, Hampshire, United Kingdom
Nottingham University Hospitals Trust
🇬🇧Nottingham, Nottinghamshire, United Kingdom
The Robert Jones and Agnes Hunt Orthopaedic Hospital NHS Foundation Trust
🇬🇧Oswestry, Shropshire, United Kingdom
Sheffield Teaching Hospitals NHS Foundation Trust
🇬🇧Sheffield, South Yorkshire, United Kingdom
The Newcastle upon Tyne Hospitals NHS Foundation Trust
🇬🇧Newcastle upon Tyne, Tyne And Wear, United Kingdom
University Hospitals Birmingham NHS Foundation Trust
🇬🇧Birmingham, West Midlands, United Kingdom
North Bristol NHS Trust
🇬🇧Bristol, United Kingdom
Research Site
🇺🇸Cambridge, Massachusetts, United States