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Active, not recruiting Phase 4 Interventional

Assessment of Potential for Chronic Liver Injury in Participants Treated With Epidiolex (Cannabidiol) Oral Solution

ClinicalTrials.gov ID: NCT05044819

Public ClinicalTrials.gov record NCT05044819. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 3:30 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Long-term Safety Study to Assess the Potential for Chronic Liver Injury in Participants Treated With Epidiolex (Cannabidiol) Oral Solution

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will monitor for potential chronic liver injury and liver fibrosis, in participants treated with cannabidiol oral solution.

Study identification

NCT ID
NCT05044819
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 4
Lead sponsor
Jazz Pharmaceuticals
Industry
Enrollment
154 participants

Conditions and interventions

Eligibility (public fields only)

Age range
1 Year and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 7, 2021 (Actual)
Primary completion
Aug 1, 2027 (Estimated)
Completion
Mar 31, 2028 (Estimated)
Last update posted
Aug 26, 2026

2021 – 2028

United States locations

U.S. sites
26
U.S. states
17
U.S. cities
25
Facility City State ZIP Site status
Clinical Trial Site Little Rock Arkansas 72758 —
Clinical Trial Site Downey California 90242 —
Clinical Trial Site Long Beach California 90806 —
Clinical Trial Site Sacramento California 95817 —
Clinical Trial Site Miami Florida 33136 —
Clinical Trial Site Miami Florida 33176 —
Clinical Trial Site Orlando Florida 32806 —
Clinical Trial Site Tampa Florida 33606 —
Clinical Trial Site Augusta Georgia 30912 —
Clinical Trial Site Wichita Kansas 67214 —
Clinical Trial Site Lexington Kentucky 40504 —
Clinical Trial Site Baltimore Maryland 21205 —
Clinical Trial Site Boston Massachusetts 02114 —
Clinical Trial Site New Brunswick New Jersey 08901 —
Clinical Trial Site New York New York 10016 —
Clinical Trial Site Charlotte North Carolina 28203 —
Clinical Trial Site Durham North Carolina 27708 —
Clinical Trial Site Cincinnati Ohio 45219 —
Clinical Trial Site Oklahoma City Oklahoma 73104 —
Clinical Trial Site Philadelphia Pennsylvania 19107 —
Clinical Trial Site Charleston South Carolina 29425 —
Clinical Trial Site Austin Texas 78758 —
Clinical Trial Site Dallas Texas 75251 —
Clinical Trial Site Houston Texas 77030 —
Clinical Trial Site Round Rock Texas 78681 —
Clinical Trial Site Winchester Virginia 22601 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05044819, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 26, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05044819 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →