GSK2862277
/ GSK
- LARVOL DELTA
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May 30, 2020
A randomised, placebo-controlled pilot study of a nebulised antitumour necrosis factor receptor-1 domain antibody in patients at risk of postoperative lung injury.
(PubMed, Eur J Anaesthesiol)
- P2 | "Pre-operative treatment with a single 26 mg inhaled dose of GSK2862277 did not result in significantly lower postoperative alveolar capillary leak or extra vascular lung water. Unexpectedly small increases in transpulmonary thermodilution-measured PVPI and extra vascular lung water index at completion of surgery suggest less postoperative lung injury than historically reported, which may have also compromised a clear assessment of efficacy in this trial. GSK2862277 was well tolerated, resulted in expected lung exposure and reduced biomarkers of lung permeability and inflammation."
Clinical • Journal • Immunology • CCL3
March 24, 2013
A Study to Investigate the Safety Tolerability Pharmacokinetics, and Pharmacodynamics of Inhaled and Intravenous GSK2862277 in Healthy Volunteers
(clinicaltrials.gov)
- P1; N=54; Completed; Sponsor: GlaxoSmithKline
Clinical • New P1 trial
November 20, 2013
A Study to Investigate the Safety Tolerability Pharmacokinetics, and Pharmacodynamics of Inhaled and Intravenous GSK2862277 in Healthy Volunteers
(clinicaltrials.gov)
- P1; N=54; Completed; Sponsor: GlaxoSmithKline; Recruiting ➔ Completed
Clinical • Trial completion
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