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RECRUITING
NCT06738017
PHASE1

Study of BMN 349 Single Dose in PiZZ and PiMZ/MASH Adult Participants

Sponsor: BioMarin Pharmaceutical

View on ClinicalTrials.gov

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

Interventions

DRUG

BMN 349

250mg oral tablet

DRUG

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