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NCT Number: NCT05103254

Bempedoic Acid Pregnancy Surveillance Program

Bempedoic acid pregnancy surveillance program

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Evidera, PPD business unit

Morrisville, North Carolina, 27560, United States

Location status: Recruiting

About this study

A surveillance study of females exposed to bempedoic acid or bempedoic acid/ezetimibe fixed combination drug product (FCDP) during pregnancy. Observational outcome data will be collected on pregnant females through pregnancy and infants through the first year of life.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Exposure to at least 1 dose of bempedoic acid or bempedoic acid/ezetimibe FCDP at any time during pregnancy (from first day of last menstrual period [LMP] to pregnancy outcome

Exclusion criteria

Treatment and study plan

Bempedoic acid

Drug

Bempedoic Acid 180 MG

Other names: Nexletol

Bempedoic Acid / Ezetimibe

Drug

Bempedoic Acid 180 MG / Ezetimibe 10 MG

Other names: Nexlizet

Primary outcomes

  1. Major congenital malformations (MCM)

    Time frame: Birth up to 12 months

    An 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 (CDC 2019a). MCMs will be defined and coded with criteria specified by US CDC Metropolitan Atlanta Congenital Defects Program (MACDP).

Secondary outcomes

  1. Minor congenital malformation

    Time frame: Birth up to 12 months

    An anomaly or abnormality of body structure that is present at birth, is of prenatal origin (i.e., birth defect), poses no significant health problem in the neonatal period, and tends to have limited social or cosmetic consequences for the affected individual (CDC 2019a). The surveillance program defines and codes minor congenital malformations with criteria specified as defined by CDC (CDC 2017).

  2. Spontaneous abortion

    Time frame: Time of conception up to birth

    An involuntary fetal loss or the expulsion of the products of conception occurring at < 20 gestational weeks.

  3. Stillbirth

    Time frame: Time of conception up to birth

    As defined by the American College of Obstetricians and Gynecologists (ACOG), an involuntary fetal loss occurring at ≥ 20 gestational weeks or, if gestational age is unknown, a fetus weighing ≥ 350 g.

  4. Elective termination

    Time frame: Time of conception up to birth

    A voluntary fetal loss or interruption of pregnancy, including pregnancy termination that occurs electively, to preserve maternal health or due to fetal abnormalities.

  5. Preterm birth

    Time frame: Time of conception up to birth

    A live birth occurring at < 37 gestational weeks.

  6. Small for gestational age (SGA)

    Time frame: Birth up to 12 months

    Weight at birth in < 10th percentile for sex and gestational age using standard growth charts for full and preterm live-born infants (Battaglia 1967). For the determination of SGA, the surveillance program will utilize the sex-specific international growth reference standards from the International Fetal and Newborn Growth Consortium for the 21st Century (INTERGROWTH-21st) for those born between 240/7 and 426/7 gestational weeks (Villar 2014; Villar 2016). The INTERGROWTH-21st standards are the latest available global reference standards, representing contemporary information from an international, multiethnic, diverse population, and have been specifically developed for modern research.

  7. Postnatal growth deficiency

    Time frame: Birth up to 12 months

    Weight in < 10th percentile for sex and chronological age using standard growth charts. Postnatal growth deficiency will be evaluated at 4 and 12 months of infant age. For the determination of postnatal growth deficiency, the surveillance program will utilize the sex-specific international growth reference standards from the World Health Organization for children ages 0 to 24 months. The World Health Organization growth standards are recommended for use in the US for infants and children 0 to 2 years of age (CDC 2010).

  8. Infant development deficiency

    Time frame: Birth up to 12 months

    Failure to achieve the developmental milestones for chronological age, as defined by the CDC (CDC 2019b). Infant developmental deficiency will be evaluated at 4 and 12 months of infant age for each CDC-defined category (social/emotional, language/communication, cognitive, and movement/physical development), separately.

Study contacts

Contact information is provided by the study sponsor or research team.

Esperion Therapuetics

CONTACT

[email protected]

1 833 377 7633 (Option 5)

Sponsors and collaborators

Lead sponsor

Esperion Therapeutics, Inc.

Industry

Registry information

Official study title

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 Women Exposed to Bempedoic Acid or Bempedoic Acid/Ezetimibe Fixed Combination Drug Product (FCDP) During Pregnancy

Important dates

Study start
2021
Primary completion
2032
Study completion
2032
First posted
Nov 2, 2021
Registry last updated
May 17, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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