A Phase 1, Open-Label, Dose-Ranging, Safety and Pharmacokinetic Study to Determine the Maximum Tolerated Dose of RX-3117 Administered Orally as a Single-Agent to Subjects With Advanced Malignancies

Trial Profile

A Phase 1, Open-Label, Dose-Ranging, Safety and Pharmacokinetic Study to Determine the Maximum Tolerated Dose of RX-3117 Administered Orally as a Single-Agent to Subjects With Advanced Malignancies

Recruiting
Phase of Trial: Phase I/II

Latest Information Update: 12 Feb 2018

At a glance

  • Drugs Fluorocyclopentenylcytosine (Primary)
  • Indications Bladder cancer; Pancreatic cancer; Solid tumours
  • Focus Adverse reactions; Therapeutic Use
  • Sponsors Rexahn Pharmaceuticals
  • Most Recent Events

    • 12 Feb 2018 According to a Rexahn Pharmaceuticals media release, total of 27 patients with advanced bladder cancer were enrolled into the study.
    • 12 Feb 2018 According to a Rexahn Pharmaceuticals media release, the data from 2a portion were presented at the American Society of Clinical Oncology Genitourinary Cancers (ASCO GU) 2018 Annual Meeting
    • 12 Feb 2018 Results published in the Rexahn Pharmaceuticals Media Release
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