Phase 1/2 Open-Label, Multiple-dose, Dose-escalation Study to Evaluate the Safety and Tolerability of IMO-8400 in Patients With Relapsed or Refractory Waldenstrom's Macroglobulinemia.

Trial Profile

Phase 1/2 Open-Label, Multiple-dose, Dose-escalation Study to Evaluate the Safety and Tolerability of IMO-8400 in Patients With Relapsed or Refractory Waldenstrom's Macroglobulinemia.

Suspended
Phase of Trial: Phase I/II

Latest Information Update: 28 Oct 2016

At a glance

  • Drugs IMO 8400 (Primary)
  • Indications Waldenstrom's macroglobulinaemia
  • Focus Adverse reactions
  • Sponsors Idera Pharmaceuticals
  • Most Recent Events

    • 28 Oct 2016 According to an Idera Pharmaceuticals media release, this trial has been suspended due to prioritization of the clinical development plans for IMO-2125, assessment showing level of clinical activity seen in the WM trial does not support monotherapy and the Companys commercial assessment of IMO-8400
    • 28 Oct 2016 Status changed from active, no longer recruiting to suspended, as reported by an Idera Pharmaceuticals media release.
    • 17 Mar 2016 Planned number of patients changed from 24 to 60 as per ClinicalTrials.gov record.
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