A Phase 3, Multicenter, Randomized, Double-Masked and Placebo-Controlled Study Evaluating the Safety of a 5.0% Concentration of Lifitegrast Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (SONATA)

Trial Profile

A Phase 3, Multicenter, Randomized, Double-Masked and Placebo-Controlled Study Evaluating the Safety of a 5.0% Concentration of Lifitegrast Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (SONATA)

Completed
Phase of Trial: Phase III

Latest Information Update: 15 Aug 2017

At a glance

  • Drugs Lifitegrast (Primary)
  • Indications Dry eyes
  • Focus Adverse reactions; Registrational
  • Acronyms SONATA
  • Sponsors SARcode Bioscience; Shire
  • Most Recent Events

    • 15 Aug 2017 According to a Shire media release, based on the data from this and other four trials (see profiles 251148, 245946, 239552 and 239399), the Marketing Authorization Application (MAA) for lifitegrast, submitted on 07 August 2017, has been validated by the UK as the Reference Member State involved in the Decentralized Procedure (DCP) MAA was submitted to Denmark, Norway, Sweden, Finland, the UK, Germany, the Netherlands, France, Italy, Portugal, Spain and Greece.
    • 17 Jun 2017 Results evaluating the combined evidence from 5 clinical trials of lifitegrast ophthalmic solution 5.0% (LIF) in subjects with dry eye disease presented at the 18th Annual Congress of the European League Against Rheumatism
    • 14 Feb 2017 According to a Shire Pharma media release, company has filed a New Drug Submission (NDS) with Health Canada for the marketing authorization of lifitegrast for the treatment of dry eye disease in adults in Canada.
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