Clinical trial

Safety and Tolerability of I.V. Infusion of MB07133 in Patients With…

NCT00073736 · Ligand Pharmaceuticals, Industry · Completed

Key facts

NCT number NCT00073736
Title Safety and Tolerability of I.V. Infusion of MB07133 in Patients With Unresectable Hepatocellular Carcinoma
Official title A Phase 1/2 Open-Label Study to Assess the Safety, Tolerability, and Pharmacokinetics of Intravenous Infusion of MB07133 in Subjects With Unresectable Hepatocellular Carcinoma and Child-Pugh Class A Liver Function
Lead sponsor Ligand Pharmaceuticals, Industry
Status Completed
Phase Phase 1/Phase 2
Study type Interventional
Conditions Hepatocellular Carcinoma
Intervention type Drug
Interventions MB07133 300mg/m2/day, MB07133 600 mg/m2/day, MB07133 1200 mg/m2/day, MB07133 1800 mg/m2/day, MB07133 2400 mg/m2/day
Enrollment 28
Start date Sep 1, 2003
Primary completion Jul 1, 2007
First posted Dec 5, 2003
Last update posted Aug 12, 2011
Countries Hong Kong, Taiwan, United States

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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