Patisiran-Lipid Nanoparticle (LNP) Pregnancy Surveillance Program
Recruiting
Observational Study
Hereditary Transthyretin-mediated (hATTR) Amyloidosis
Polyneuropathy
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Sex
- Female
- Study type
- Observational
- Participants needed
- 10 (estimated)
- Sponsor
- Alnylam Pharmaceuticals · Industry
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About This Trial
The purpose of this study is to collect and evaluate pregnancy outcomes, pregnancy complications, and fetal/neonatal/infant outcomes in women exposed to patisiran-LNP.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Documentation that the patient was exposed to patisiran-LNP at any point starting from 12 weeks before LMP or at any point during pregnancy
Exclusion Criteria:
* There are no exclusion criteria for participation in this program.
Contacts