Condition: Transthyretin Amyloidosis · Sponsor: AstraZeneca
The overall objective of this DPSS is to describe the occurrence of pregnancy and maternal complications, adverse effects on the developing fetus and neonate, and adverse effects on the infant associated with exposure to eplontersen during pregnancy and/or lactation.
This description comes directly from the study's public registry record.
AstraZeneca Clinical Study Information Center · 1-877-240-9479 · information.center@astrazeneca.com
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| Research Site | Frankfurt, Germany | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07205666