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AEterna Zentaris Inc.

www.aezsinc.com

Latest From AEterna Zentaris Inc.

FDA Achieves Historically Low Eight-Month Median Drug Review Time In 2017

Median review times for US agency's drug center were 10 months from 2011 to 2013, and 11 months from 2015 to 2016.

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FDA Bests Annual Novel Drug Approval Record With Four Oks In One Week

The agency's Dec. 21 approval of Giapreza became novel drug No. 46 of 2017, topping the 2015 mark of 45.

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Pipeline Watch: Phase III Starts For BL-8040, Trigriluzole, MIN-101

Pipeline Watch is a weekly snapshot of selected late-stage clinical trial events announced by pharmaceutical and biotech companies at medical and industry conferences, in financial and company presentations, and in company releases and statements.

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Keeping Track: Approvals, A Burst Of Submissions, And Some Priority Reviews

The latest drug development news and highlights from our US FDA Performance Tracker.

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Company Information

  • Industry
  • Biotechnology
  • Pharmaceuticals
  • Therapeutic Areas
  • Cancer
  • Gynecological, Urological
  • Metabolic Disorders
  • Alias(es)
  • AEterna Laboratories Inc.
  • Ownership
  • Public
  • Headquarters
  • Worldwide
    • North America
      • USA
  • Parent & Subsidiaries
  • AEterna Zentaris Inc.
  • Senior Management
  • David Dodd, Pres. & CEO
    Richard Sachse, MD, PhD, SVP, CSO & CMO
    Jude Dinges, SVP, Chief Commercial Officer
  • Contact Info
  • AEterna Zentaris Inc.
    Phone: (843) 900-3223
    315 Sigma Dr.
    Ste. 302D
    Charleston, SC 29486
    USA
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