Clin2
NCT04270058Possibly a fitNot yet recruiting

Tracking TEGSEDI safety during pregnancy

Hereditary Transthyretin-mediated Amyloidosis With PolyneropathyPregnancy

Part of Brain & nervous system, Genetic & congenital, Women’s health & pregnancy clinical trials.

This study tracks the safety of the medicine TEGSEDI during pregnancy for women with hATTR-PN, a rare genetic nerve condition. It compares outcomes between those who took TEGSEDI while pregnant and those who did not, to better understand any risks.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
20 people
Ages
Any age
Study type
Observational

Who can take part

  • You are pregnant and have taken TEGSEDI within 25 weeks before conception or during pregnancy, OR you are pregnant and have a diagnosis of hATTR-PN but have not taken TEGSEDI.
  • You are willing and able to provide informed consent.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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