Plain-English translation of NCT05040373 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This is a safety monitoring program for women who are pregnant or planning to become pregnant while taking patisiran, a medication used to treat hereditary transthyretin-mediated amyloidosis (a rare nerve disease). Researchers want to gather real-world information about how pregnancy progresses, any complications that occur, and the health of babies born to women exposed to this medication. This helps doctors understand whether the medication is safe to use during pregnancy.
When women with rare diseases need ongoing medication, doctors need good information about whether that medication might affect pregnancy or the developing baby. This program fills that gap by collecting and studying actual pregnancy experiences from women taking this medication.
You likely qualify if…
You likely don't qualify if…
You would share medical records and information about your pregnancy, any complications you experienced, and your baby's health after birth. This is not an experimental study where you take a new medication — instead, you're providing information about a medication you're already taking or have already taken. The program aims to enroll about 10 women total and involves sharing your existing medical information with the research team.
AI-generated summary from trial data · Jun 1, 2026 · Not medical advice
United States
France
Germany
Italy
Netherlands
Sponsor
Alnylam Pharmaceuticals
Enrollment target
~10 participants
Started
August 2020
Primary completion
October 2030
Sex
Female only
Last updated on clinicaltrials.gov in June 2026.
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Central contact
Alnylam Clinical Trial Information Line
Alnylam Pharmaceuticals
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