HomeTrialNCT04632953
🔬NCT04632953ACTIVE NOT RECRUITING

Long-Chain Fatty Acid Oxidation Disorders In-Clinic Disease Monitoring Program

Study Summary

The primary objective of this study is to assess the long-term safety, including pregnancy, infant, and lactation outcomes, of patients with LC-FAOD who are enrolled in the DMP.

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment150 participants
Primary Completion
Lead SponsorUltragenyx Pharmaceutical Inc
Data Retrieved2026-04-11 04:25:35.045646+00:00
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