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Clinuvel Pharmaceuticals LimitedASX: CUV

FDA awards SCENESSE Fast Track designation for EPP treatment

Jul 5, 2016 at 10:48 PM EDT · Issued by Clinuvel Pharmaceuticals Limited

Filed with ASX · Jul 5, 2016 at 10:48 PM EDT · 3 pages · English

On 6ix: 6ix.com/news/fda-awards-scenesse-fast-track-designation-for-epp-treatment

Watch Clinuvel Pharmaceuticals' latest callClinuvel Pharmaceuticals (ASX:CUV) Q4 2026 Earnings Call · Replay · Aug 27↗

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Earlier from Clinuvel Pharmaceuticals

  • SCENESSE launched in EuropeJun 22, 2016
  • SCENESSE Treatment in EuropeMay 18, 2016
  • SCENESSE attains breakthrough European Market AuthorisationMar 30, 2016
  • US patent for alpha-MSH and analoguesMar 30, 2016
  • Patent to assist drug as potential skin cancer preventativeMar 30, 2016

Later from Clinuvel Pharmaceuticals

  • FDA accept SCENESSE clinical data package for NDA submissionJul 18, 2016
  • Clinuvel completes combination therapy pre-clinical studyAug 3, 2016
  • FDA Schedules Pre-NDA Meeting for SCENESSEOct 12, 2016
  • SCENESSE - NICE England UpdateOct 17, 2016
  • CLINUVEL agrees with FDA on New Drug Application timelinesNov 8, 2016
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