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A Study to Assess the Amount of Palopegteriparatide in Breast Milk of Lactating Females Requiring YORVIPATH® (Palopegteriparatide)

NCT07264634 RECRUITING

This is an observational, opportunistic lactation study to be conducted in lactating female participants who are currently receiving therapeutic doses of YORVIPATH as part of their usual care and who have chosen to breastfeed their infant(s). The potential transfer of palopegteriparatide into breast milk will be assessed.

Details

Lead sponsorAscendis Pharma A/S
StatusRECRUITING
Enrolment10
Start date2026-03-19
Completion2028-01

Conditions

Interventions

Primary outcomes

Countries

United States