Last reviewed · How we verify
NCT02614872
Study to Evaluate the Safety and Efficacy of Intravenous Glassia® Treatment in Lung Transplantation
Phase 2 trial testing GLASSIA® and Institution standard of care (SOC) in Transplantation, Lung Rejection in 30 participants. Completed in 7 May 2019.
11 April 2019
Quick facts
| Lead sponsor | Kamada, Ltd. |
|---|---|
| Phase | Phase 2 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 30 |
| Start date | 26 July 2016 |
| Primary completion | 11 April 2019 |
| Estimated completion | 7 May 2019 |
| Sites | 1 location across Israel |
Drugs / interventions tested
- GLASSIA® and Institution standard of care (SOC) — full drug profile →
Conditions studied
- Transplantation, Lung Rejection — all drugs for Transplantation, Lung Rejection →
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):
-
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 -
The COPD Pipeline XXX.
Gross N. · · 2015 · cited 1× · PMID 28848873 · DOI 10.15326/jcopdf.3.1.2015.0181
Verify or expand the search:
- PubMed search for NCT02614872
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other Kamada, Ltd. trials
Trials by the same sponsor.
- NCT04550325 — Safety, PK and PD of Kamada Anti-SARS-CoV-2 in COVID-19 · Phase 1, PHASE2 · completed
- NCT02912845 — Post-marketing Study of KamRAB Administered as a Single Dose With Active Rabies Vaccine in Children Exposed to Rabies · Phase 3 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT02614872 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Kamada, Ltd.
- Last refreshed: 1 September 2021
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