Clinical trial

Efficacy Study of DX-88 (Ecallantide) to Treat Acute Attacks of Hereditary…

NCT00457015 · Shire, Industry · Completed

Key facts

NCT number NCT00457015
Title Efficacy Study of DX-88 (Ecallantide) to Treat Acute Attacks of Hereditary Angioedema (HAE)
Official title EDEMA4: A Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study to Assess the Efficacy and Safety of DX-88 (Ecallantide) for the Treatment of Acute Attacks of Hereditary Angioedema
Lead sponsor Shire, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Hereditary Angioedema (HAE)
Intervention type Drug
Interventions ecallantide, Phosphate Buffer Saline (PBS), pH 7.0
Enrollment 96
Start date Apr 1, 2007
Primary completion Jun 1, 2008
Completion Jun 1, 2008
First posted Apr 5, 2007
Last update posted Jun 8, 2021
Countries Canada, Jordan, United States

At a glance

  • 10–99 Study sites
  • Yes 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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