A Phase 1a Open-Label, Dose-Escalation Study of the Safety and Pharmacokinetics of OMP-313M32 Administered as a Single Agent to Subjects With Locally Advanced or Metastatic Solid Tumors

Trial Profile

A Phase 1a Open-Label, Dose-Escalation Study of the Safety and Pharmacokinetics of OMP-313M32 Administered as a Single Agent to Subjects With Locally Advanced or Metastatic Solid Tumors

Recruiting
Phase of Trial: Phase I

Latest Information Update: 28 Jul 2017

At a glance

  • Drugs OMP 313M32 (Primary)
  • Indications Solid tumours
  • Focus Adverse reactions
  • Sponsors OncoMed Pharmaceuticals
  • Most Recent Events

    • 09 May 2017 According to an OncoMed Pharmaceuticals media release, Johanna Bendell, M.D., Associate Director of the Drug Development Program at Sarah Cannon Research Institute is a lead investigator for the study.
    • 04 May 2017 According to an OncoMed Pharmaceuticals media release, first patient has been dosed in the study.
    • 26 Apr 2017 Status changed from not yet recruiting to recruiting.
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