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Study of BMN 349 Single Dose in PiZZ and PiMZ/MASH Adult Participants
Sponsor: BioMarin Pharmaceutical
Summary
The goal of this clinical trial is to assess the safety and tolerability of a single oral dose of BMN 349 in participants with PiZZ or PiMZ/MASH. Primary outcome measures include incidence of any adverse events (including serious adverse events, dose limit toxicities, and adverse events of special interest), incidence of any laboratory test abnormalities, incidence of lung function test abnormalities and 12-lead ECG parameters. Participants will receive a single dose of either BMN 349 or placebo and then monitored for safety and tolerability.
Official title: A Randomized, Double-Blind, Placebo-Controlled, Single Oral Dose Study Evaluating the Safety and Pharmacokinetics of BMN 349 in Homozygous for the Z Mutation of Alpha 1 Antitrypsin Gene (PiZZ) and Heterozygous for the Z Mutation (PiMZ/MASH)
Key Details
Gender
All
Age Range
18 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
12
Start Date
2025-02-21
Completion Date
2025-09
Last Updated
2025-09-08
Healthy Volunteers
No
Conditions
Interventions
BMN 349
250mg oral tablet
Placebo
250mg oral tablet
Locations (8)
University of California, San Diego
San Diego, California, United States
Saint Louis University
St Louis, Missouri, United States
Medpace Clinical Pharmacology Unit
Cincinnati, Ohio, United States
The Medical University of South Carolina
Charleston, South Carolina, United States
NHS Lothian
Edinburgh, UK, United Kingdom
Royal Free London NHS Foundation Trust
London, UK, United Kingdom
Nottingham University Hospitals
Nottingham, UK, United Kingdom
University Hospital Southampton NHS Foundation Trust
Southampton, UK, United Kingdom