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Pregnancy Surveillance Program of Patients Exposed to Epidiolex/Epidyolex During Pregnancy

Pregnancy Surveillance Program of Patients Exposed to Epidiolex/Epidyolex During Pregnancy

Recruiting
Female
Phase N/A
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Overview

The purpose of this study is to evaluate pregnancy-related health outcomes in participants who are exposed to Epidiolex/Epidyolex during pregnancy and their infant up to 12 months of life.

Eligibility

Inclusion Criteria:

  1. Patients with exposure to at least 1 dose of Epidiolex/Epidyolex during the 13 days prior to their LMP or at any time during pregnancy.
  2. Verbal or written informed consent to participate

Exclusion criteria:

  1. Patients exposed to a non-regulatory approved product containing Cannabidiol (CBD) during pregnancy who do not also have exposure to Epidiolex during the 13 days prior to their LMP or during the pregnancy.

Study details
    Maternal Complications
    Pregnancy Complication
    Birth Outcomes
    Adverse
    Pregnancy

NCT06113237

Jazz Pharmaceuticals

21 July 2025

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