Clinical trial

Pharmacokinetics of Patupilone After a Single Intravenous Administration in…

NCT00426140 · Novartis Pharmaceuticals, Industry · Completed

Key facts

NCT number NCT00426140
Title Pharmacokinetics of Patupilone After a Single Intravenous Administration in Patients With Advance Solid Tumor Malignancies.
Official title An Open-label Single Center Study to Characterize the Absorption, Distribution, Metabolism, and Elimination (ADME) of Patupilone (EPO906) After a Single Intravenous Administration of 10 mg/m2 [14C] Patupilone in Patients With Advanced Solid Tumor Malignancies.
Lead sponsor Novartis Pharmaceuticals, Industry
Status Completed
Phase Phase 1
Study type Interventional
Conditions Advanced Malignancies, Solid Tumors
Intervention type Drug
Interventions Patupilone
Enrollment 5
Start date Aug 1, 2006
Primary completion Nov 1, 2006
First posted Jan 24, 2007
Last update posted Dec 8, 2020
Countries 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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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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