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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

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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

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 27 Nov 2017

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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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