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Odevixibat Pregnancy and Lactation Surveillance Program: A Study to Evaluate the Safety of Odevixibat During Pregnancy and/or Lactation

Odevixibat Pregnancy and Lactation Surveillance Program: A Post-marketing, Long-term, Observational, Descriptive Study to Assess the Risk of Pregnancy and Maternal Complications and Adverse Effects on the Developing Fetus, Neonate, and Infant Among Individuals Exposed to Odevixibat During Pregnancy and/or Lactation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06258902
Enrollment
20
Registered
2024-02-14
Start date
2023-09-28
Completion date
2032-05-31
Last updated
2026-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy Related

Keywords

Rare disease, PFIC, Pregnancy, Lactation

Brief summary

The participants of this study will be of any age who are exposed to at least 1 dose of odevixibat at any time during pregnancy (from 1 day prior to conception to pregnancy outcome) and/or at any time during lactation (up to 12 months of infant age or weaning, whichever comes first. This study will collect data obtained via a variety of sources, including enrolled pregnant or lactating participants, the healthcare providers (HCP) involved in their care or the care of their infants, if applicable, and Albireo pharmacovigilance. Study start date is either start of data collection or first patient enrolled whatever occurs earlier. The surveillance program is strictly observational; the schedule of office visits and all treatment regimens are determined by HCPs. Only data that are routinely documented in patients' medical records as part of usual care will be collected. No additional laboratory tests or HCP assessments will be required as part of this surveillance program.

Interventions

None listed

Sponsors

Ipsen
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE

Inclusion criteria

* Exposure to at least 1 dose of odevixibat at any time during pregnancy (from 1 day prior to conception to pregnancy outcome) and/or at any time during lactation (up to 12 months of infant age or weaning, whichever comes first). * Informed consent or IRB-/EC-approved waiver of informed consent (not applicable if reported by Albireo PV according to usual pharmacovigilance practices)

Exclusion criteria

* Refusal to provide informed consent, if required

Design outcomes

Primary

MeasureTime frameDescription
Prevalence rate of major congenital malformations (MCM) at birthAt birthAn abnormality of body structure or function that is present at birth; is of prenatal origin (i.e. birth defect); has significant medical, social or cosmetic consequences for the affected individual; and typically requires medical intervention.

Secondary

MeasureTime frameDescription
Prevalence rate of minor congenital malformations at birthAt birth
Prevalence rate of molar or ectopic pregnancyThroughout pregnancy, an average of 9 monthsMolar pregnancy is defined as an abnormal pregnancy that happens when a sperm fertilizes an egg that does not contain any genetic material. Ectopic pregnancy is defined as a pregnancy that occurs outside of the uterine cavity, usually in one of the fallopian tubes.
Prevalence rate of fetal lossThroughout pregnancy, an average of 9 monthsA fetal loss that occurs for any reason at any time during pregnancy. This includes spontaneous abortion (SAB), stillbirth, elective or therapeutic abortion, fetal loss (type not specified).
Prevalence rate of live birthAt birthThe birth of a living fetus at ≥ 20 gestational weeks or, if gestational age is unknown, weighing ≥ 350g.
Prevalence rate of preterm birthAt birth
Prevalence rate of small for gestational age (SGA)At birthBirth weight \<10th percentile for sex and gestational age using standard growth charts for full and preterm live-born infants.
Prevalence rate of neonatal deathWithin the first 28 days of life
Prevalence rate of infant deathThroughout the first year of life
Prevalence rate of postnatal growth deficiencyThroughout the first year of lifeWeight, length or head circumference in \<10th percentile for sex and age using standard growth charts.
Prevalence rate of infant developmental delayThroughout the first year of lifeFailure to achieve the developmental milestones for chronological age, as defined by the Centers for Disease Control and Prevention (CDC)
Prevalence rate of infant hospitalization due to serious illnessThroughout the first year of lifeInfant hospital visit due to a serious (i.e. results in significant disability, incapacity, or death; is life-threatening; requires inpatient or prolonged hospitalization; or is considered medically important)

Countries

United States

Contacts

CONTACTIpsen Clinical Study Enquiries
clinical.trials@ipsen.comSee e mail
STUDY_DIRECTORIpsen Medical Director

Ipsen

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 1, 2026