drugset / Trial / NCT01335958

Safety and Pharmacokinetics of DMUC5754A Administered Intravenously to Patients With Platinum-Resistant Ovarian Cancer or Unresectable Pancreatic Cancer

NCT01335958 ↗

Phase 1 Completed 77 enrolled Genentech, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is a Phase I, multi-center, open-label, dose-escalation study of DMUC5754A administered as a single agent by intravenous (IV) infusion to patients with platinum-resistant ovarian cancer or unresectable pancreatic cancer.

Timeline

Start
2011-04
Primary completion
2014-02
Completion
2014-02

Drugs

EvaluationDrugModalityDoseRoute
Subject SOFITUZUMAB VEDOTIN Unknown 0.3 mg/kg Intravenous
Subject SOFITUZUMAB VEDOTIN Unknown 0.8 mg/kg Intravenous
Subject SOFITUZUMAB VEDOTIN Unknown 1.6 mg/kg Intravenous
Subject SOFITUZUMAB VEDOTIN Unknown 3.2 mg/kg Intravenous