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Clinical Trials in the EU / 2022-502911-12-00
Completed Phase I/II

A Phase 1/2, Global, Open-Label, Extension Study to Evaluate the Long-Term Safety and Clinical Activity of mRNA-3927 in Participants Previously Enrolled in the mRNA-3927-P101 Study

2022-502911-12-00 · tracked via the Priya Life Science EU tracker
Sponsor
Moderna Inc.
Sponsor type
Pharmaceutical company
Therapeutic area
Nutritional and Metabolic Diseases
Decision date
23/02/2026
Enrollment target
13
Sites
Spain, Netherlands, France

Condition studied

Propionic Acidemia

Investigational medicinal product(s)

mRNA-3927

Eligibility

Age group
0-17 years, 18-64 years
Sex
Female, Male

Primary endpoint

Incidence and severity of AEs (including mRNA-3927 -related and not related AEs), SAEs, and AEs leading to treatment discontinuation.

Endpoint detail

Annualized frequency of Investigator-reported MDEs., Annualized frequency of Investigator-reported MDE-related hospitalizations., Annualized frequency of Investigator-reported PA-related hospitalizations., Annualized frequency of Investigator-reported PA-related urgent healthcare encounters.

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2022-502911-12-00 on CTIS ↗ ← All trials in the EU