The purpose of this post-marketing study is to assess the amount of guselkumab in breast milk of lactating women receiving guselkumab as part of their standard clinical care provided by their treating physician, for any of the approved indications.
Age range
18 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Guselkumab Concentrations at Steady State in Breast Milk (Q4W Maintenance Regimen)
Timeframe: Up to Day 29
Guselkumab Concentrations at Steady State in Breast Milk (Q8W Maintenance Regimen)
Timeframe: Up to Day 57
Estimated Daily Infant Dosage of Guselkumab Q4W Maintenance Regimen
Timeframe: Up to Day 29
Estimated Daily Infant Dosage of Guselkumab Q8W Maintenance Regimen
Timeframe: Up to Day 57