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A Multicenter, Randomized, Open-Label, Controlled Trial to Assess the Safety and Tolerability of Lucinactant for Inhalation in Preterm Neonates 29 to 34 Weeks PMA: Dose Escalation and Study Extension

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Trial Profile

A Multicenter, Randomized, Open-Label, Controlled Trial to Assess the Safety and Tolerability of Lucinactant for Inhalation in Preterm Neonates 29 to 34 Weeks PMA: Dose Escalation and Study Extension

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 14 Jan 2020

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At a glance

  • Drugs Sinapultide (Primary)
  • Indications Neonatal respiratory distress syndrome
  • Focus Adverse reactions
  • Sponsors Discovery Laboratories; Windtree Therapeutics

    • Most Recent Events

    • 28 Nov 2016 Results published in the Windtree Therapeutics Media Release
    • 28 Nov 2016 According to a Windtree Therapeutics media release, data from this trial was presented at the 6th International Congress of European Neonatal and Perinatal Societies (UENPS)
    • 28 Apr 2016 According to a Windtree Therapeutics media release, data from this study will be presented as a poster at the 2016 Pediatric Academic Societies (PAS) Meeting 2016.

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