RecruitingNCT05040373

Patisiran-Lipid Nanoparticle (LNP) Pregnancy Surveillance Program

Patisiran-LNP Pregnancy Surveillance Program


Sponsor

Alnylam Pharmaceuticals

Enrollment

10 participants

Start Date

Aug 1, 2020

Study Type

OBSERVATIONAL

Conditions

Summary

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.


Eligibility

Sex: FEMALE

Inclusion Criteria1

  • Documentation that the patient was exposed to patisiran-LNP at any point starting from 12 weeks before LMP or at any point during pregnancy

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Locations(7)

Clinical Trial Site

Iowa City, Iowa, United States

Clinical Trial Site

Nantes, France

Clinical Trial Site

Münster, Germany

Clinical Trial Site

Pavia, Italy

Clinical Trial Site

Groningen, Netherlands

Clinical Trial Site

Lisbon, Portugal

Clinical Trial Site

Madrid, Spain

View Full Details on ClinicalTrials.gov

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NCT05040373


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