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A Study to Assess the Amount of Palopegteriparatide in Breast Milk of Lactating Females Requiring YORVIPATH® (Palopegteriparatide)
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 sponsor | Ascendis Pharma A/S |
|---|---|
| Status | RECRUITING |
| Enrolment | 10 |
| Start date | 2026-03-19 |
| Completion | 2028-01 |
Conditions
- Hypoparathyroidism
Interventions
- Palopegteriparatide
Primary outcomes
- To evaluate the transfer of palopegteriparatide into human breast milk of lactating female participants who are breastfeeding while being treated with YORVIPATH — 6 days
Countries
United States