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Trials / Recruiting

RecruitingNCT04846959

Study to Evaluate Pregnancy Outcomes in Risankizumab Exposed Pregnancies Relative to Those Non-risankizumab Exposed Pregnancies in Women With FDA Approved Indications

Risankizumab Pregnancy Exposure Registry: a Prospective Observational Study on the Safety of Risankizumab Exposure in Pregnant Women and Their Offspring

Status
Recruiting
Phase
Study type
Observational
Enrollment
818 (estimated)
Sponsor
AbbVie · Industry
Sex
Female
Age
Healthy volunteers
Not accepted

Summary

The objective of this registry is to compare outcomes of risankizumab-exposed pregnancies with those of pregnancies that were not exposed to risankizumab among women with plaque psoriasis, psoriatic arthritis (PsA), Crohn's disease (CD), or other conditions for which risankizumab is an FDA-approved treatment. The registry is designed to estimate the association between risankizumab and maternal, fetal, and infant outcomes by comparing the prevalence rates of these outcomes in the exposed and unexposed populations. Approximately 818 female participants with pregnancy will be enrolled (409 participants exposed to risankizumab and 409 without exposure) at multiple sites across the United States. Participants will not receive risankizumab as part of this study. Maternal and fetal outcomes during pregnancy for female participants who received risankizumab or other treatment will be followed for and up to 1 year after delivery There may be a higher burden for participants in this study compared to standard of care. Participants will attend visits determined by HCPs during the study at a hospital or clinic. The pregnancy outcomes including side effects will be collected during routine clinical care.

Conditions

Interventions

TypeNameDescription
DRUGRisankizumabSubcutaneous Injection
DRUGComparatorSubcutaneous or Intravenous Injection

Timeline

Start date
2021-07-30
Primary completion
2032-06-01
Completion
2032-06-01
First posted
2021-04-15
Last updated
2025-07-17

Locations

2 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04846959. Inclusion in this directory is not an endorsement.