clinical trial · NCT07345494
A Global Pregnancy Registry to Assess Maternal, Fetal, and Infant Outcomes Following Exposure to YORVIPATH® (Palopegteriparatide) During Pregnancy and Breastfeeding
HypoparathyroidismPalopegteriparatide
brief summary
The purpose of this registry study is to collect both prospective and retrospective data in women exposed to palopegteriparatide during pregnancy to assess risk of pregnancy and maternal complications, and adverse effects on the developing fetus, neonate, and infant and to assess infant outcomes through at least the first year of life.
started
Feb 18, 2026
primary completion
Jan 1, 2036
completion
Jan 1, 2036
last updated
Mar 2, 2026
sourced from ClinicalTrials.gov · pharmadog mirrors structured fields, not the full protocol