Dose Escalation, Safety, Pharmacokinetic and Pharmacodynamic, First in Man Study, of SAR125844 Single Agent Administered as Slow Intravenous Infusion in Adult Patients With Advanced Malignant Solid Tumors

Trial Profile

Dose Escalation, Safety, Pharmacokinetic and Pharmacodynamic, First in Man Study, of SAR125844 Single Agent Administered as Slow Intravenous Infusion in Adult Patients With Advanced Malignant Solid Tumors

Completed
Phase of Trial: Phase I

Latest Information Update: 13 Nov 2017

At a glance

  • Drugs SAR 125844 (Primary)
  • Indications Solid tumours
  • Focus Adverse reactions; First in man; Therapeutic Use
  • Acronyms SARMET
  • Sponsors Sanofi
  • Most Recent Events

    • 13 Nov 2017 Results assessing antitumor response and safety, published in the European Journal of Cancer.
    • 02 Feb 2016 Planned End Date changed from 1 May 2017 to 1 Apr 2017, as reported by the ClinicalTrials.gov record.
    • 02 Feb 2016 Planned primary completion date changed from 1 May 2017 to 1 Apr 2017, as reported by the ClinicalTrials.gov record.
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