A Phase 2 Open-Label Study to Assess the Pharmacodynamics, Pharmacokinetics, Safety and Tolerability of AKCEA-ANGPTL3-LRX (ISIS 703802) Administered Subcutaneously to Patients With Familial Chylomicronemia Syndrome (FCS)

Trial Profile

A Phase 2 Open-Label Study to Assess the Pharmacodynamics, Pharmacokinetics, Safety and Tolerability of AKCEA-ANGPTL3-LRX (ISIS 703802) Administered Subcutaneously to Patients With Familial Chylomicronemia Syndrome (FCS)

Recruiting
Phase of Trial: Phase II

Latest Information Update: 16 Feb 2018

At a glance

  • Drugs IONIS ANGPTL3 LRx (Primary)
  • Indications Hyperlipoproteinaemia type I
  • Focus Therapeutic Use
  • Sponsors Akcea Therapeutics; Ionis Pharmaceuticals
  • Most Recent Events

    • 07 Feb 2018 Planned End Date changed from 31 Jul 2018 to 30 Sep 2018.
    • 07 Feb 2018 Planned primary completion date changed from 30 Apr 2018 to 30 Jul 2018.
    • 06 Dec 2017 Status changed from not yet recruiting to recruiting.
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