CLINICAL TRIALS PROFILE FOR SURFAXIN
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All Clinical Trials for SURFAXIN
Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
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NCT00215540 ↗ | SURFAXIN® Treatment for Prevention of Bronchopulmonary Dysplasia (BPD) in Very Low Birth Weight (VLBW) Infants. | Terminated | Windtree Therapeutics | Phase 2 | 2005-02-01 | SURFAXIN® (lucinactant) treatment will be examined in very low birth weight infants to prevent development of chronic lung disease, commonly known as bronchopulmonary dysplasia (BPD), in premature infants who have required continued intubation and received surfactants for the prevention or treatment of respiratory distress syndrome (RDS). |
NCT00215553 ↗ | KL₄Surfactant Treatment in Patients With ARDS | Terminated | Windtree Therapeutics | Phase 2 | 2001-05-01 | Lung wash with KL₄Surfactant of individual lung segments using a bronchoscope compared to usual care alone consisting primarily of assisted (mechanical) ventilation in patients with acute respiratory distress syndrome(ARDS). |
NCT00807235 ↗ | Feasibility Study of Aerosolized Surfaxin in the Prevention of Respiratory Distress Syndrome (RDS) in Premature Infants | Terminated | Windtree Therapeutics | Phase 2 | 2005-01-01 | To evaluate the feasibility, safety and tolerability of aerosolized lucinactant delivered by nasal continuous positive airway pressure (nCPAP) for the prevention of respiratory distress syndrome (RDS) in premature infants. |
NCT04389671 ↗ | The Safety and Preliminary Tolerability of Lyophilized Lucinactant in Adults With Coronavirus Disease 2019 (COVID-19) | Recruiting | Windtree Therapeutics | Phase 2 | 2020-11-02 | This is a multicenter, single-treatment study. Subjects will consist of adults with COVID-19 associated acute lung injury who are being cared for in a critical care environment. |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
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