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NCT02614872

Study to Evaluate the Safety and Efficacy of Intravenous Glassia® Treatment in Lung Transplantation

Completed Phase 2 Last updated 1 September 2021
What this trial tests

Phase 2 trial testing GLASSIA® and Institution standard of care (SOC) in Transplantation, Lung Rejection in 30 participants. Completed in 7 May 2019.

Timeline
26 July 2016
Primary endpoint
11 April 2019
7 May 2019

Quick facts

Lead sponsorKamada, Ltd.
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment30
Start date26 July 2016
Primary completion11 April 2019
Estimated completion7 May 2019
Sites1 location across Israel

Drugs / interventions tested

Conditions studied

Sponsor

Kamada, Ltd. — full company profile →

Who can join

18 and older, any sex, with Transplantation, Lung Rejection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study evaluates the safety and efficacy of intravenous GLASSIA® treatment in lung transplantation.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Alpha-1 Antitrypsin Substitution for Extrapulmonary Conditions in Alpha-1 Antitrypsin Deficient Patients.
    Baranovski BM, Schuster R, Nisim O, Brami I, et al · · 2018 · cited 8× · PMID 30723784 · DOI 10.15326/jcopdf.5.4.2017.0161
  2. The COPD Pipeline XXX.
    Gross N. · · 2015 · cited 1× · PMID 28848873 · DOI 10.15326/jcopdf.3.1.2015.0181

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Other Kamada, Ltd. trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02614872.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing