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Bempedoic Acid Pregnancy Surveillance Program

Esperion Therapeutics logo

Esperion Therapeutics

Status

Enrolling

Conditions

Hyperlipidemias
Pregnancy

Treatments

Drug: Bempedoic Acid / Ezetimibe
Drug: Bempedoic Acid

Study type

Observational

Funder types

Industry

Identifiers

NCT05103254
1002-074

Details and patient eligibility

About

Bempedoic acid pregnancy surveillance program

Full description

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.

Enrollment

20 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

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:

Trial contacts and locations

1

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Central trial contact

Esperion Therapuetics

Data sourced from clinicaltrials.gov

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