GLASSIA Safety, Immunogenicity, and Bronchoalveolar Lavage Study

PHASE3CompletedINTERVENTIONAL
Enrollment

34

Participants

Timeline

Start Date

March 8, 2016

Primary Completion Date

July 29, 2020

Study Completion Date

July 29, 2020

Conditions
Alpha1-antitrypsin Deficiency
Interventions
BIOLOGICAL

GLASSIA

Participants will receive weekly IV infusions of GLASSIA at 60 mg/kg BW active A1PI protein administered at a rate of 0.2 mL/kg/min for 25 weeks (25 planned infusions) via an IV administration.

Trial Locations (18)

19140

Temple University School of Medicine, Philadelphia

21286

Pulmonary Critical Care Associates of Baltimore, Towson

27103

Southeastern Research Center LLC, Winston-Salem

29425

Medical University of South Carolina (MUSC), Charleston

33136

University of Miami, Miami

33321

DBC Research Corp, Pembroke Pines, Tamarac

33331

Cleveland Clinic Florida - Weston, Weston

45415

Dayton Respiratory Research Center, Dayton

46360

LaPorte County Institute for Clinical Research, Inc., Michigan City

60637

University of Chicago Medical Center, Chicago

63401

Hannibal Clinic, Hannibal

75708

University of Texas Health Science Center at Tyler, Tyler

77005

Renovatio Clinical-Respiratory & Sleep Disorders Specialists, The Woodlands

85724

Arizona Board of Regents, University of Arizona, Tucson

90024

UCLA Medical Center, Los Angeles

90048

Cedars Sinai Medical Center, Division of Pulmonary and Critical Care Medicine, Los Angeles

95817

University of California Davis Health System, Sacramento

N6A 5W9

LHSC - Victoria Hospital, London

All Listed Sponsors
lead

Baxalta now part of Shire

INDUSTRY

NCT02525861 - GLASSIA Safety, Immunogenicity, and Bronchoalveolar Lavage Study | Biotech Hunter | Biotech Hunter