A Research Study Looking Into the Effect of NNC0519-0130 on Blood Levels of a Birth Control Pill and Emptying of the Stomach in Women After Menopause
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Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Na · None · Treatment
Enrollment
47actual
Sites
1
Country
Germany
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2024-07-18 | actual | When the study began enrolling |
| Primary completion | 2025-09-10 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2025-09-30 | actual | The whole study's end, after follow-up |
| First posted | 2024-07-22 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-03-12 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Diabetes Mellitus, Type 2
Interventions
- Drug: NNC0519-0130
- Drug: Levonorgestrel + Ethinylestradiol
- Drug: Paracetamol
Primary outcomes
what the primary-completion date above is the date OFArea under the ethinylestradiol plasma concentration time curve during a dosing interval at steady state
measured Day 8
Area under the ethinylestradiol plasma concentration time curve during a dosing interval at steady state
measured Day 188
Area under the levonorgestrel plasma concentration time curve during a dosing interval at steady state
measured Day 8
Area under the levonorgestrel plasma concentration time curveduring a dosing interval at steady state
measured Day 188
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