Clinical trial

Toxicities Associated With Subcutaneous Administration of Ethyol (Amifostine)…

NCT00130143 · The Dale & Frances Hughes Cancer Center, Other · Completed

Key facts

NCT number NCT00130143
Title Toxicities Associated With Subcutaneous Administration of Ethyol (Amifostine) for the Prevention of Radiation-Induced Toxicities
Official title Open-Label Prospective Trial Evaluating the Toxicities Associated With Subcutaneous Administration of Ethyol (Amifostine) for the Prevention of Radiation-Induced Toxicities
Lead sponsor The Dale & Frances Hughes Cancer Center, Other
Collaborators MedImmune LLC Industry
Status Completed
Study type Interventional
Conditions Head and Neck Cancer, Lung Cancer
Intervention type Drug
Interventions Ethyol (Amifostine)
Enrollment 20
Start date Jun 1, 2003
Completion Sep 1, 2004
First posted Aug 15, 2005
Last update posted Sep 27, 2005
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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