CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 75 enrolled
Drug / intervention
recombinant human C1 inhibitor +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00262301
NCT00262301Phase 3Completed

A Randomized, Placebo-controlled, Double-blind Phase III Study of the Efficacy and Safety of Recombinant Human C1 Inhibitor for the Treatment of Acute Attacks in Patients With Hereditary Angioedema

Pharming Technologies B.V.·interventional·Posted Dec 6, 2005·Updated Oct 2, 2012

In Brief

A Phase 3 clinical trial evaluating recombinant human C1 inhibitor and Placebo for Hereditary Angioedema and 2 related conditions. Completed, enrolled 75 participants across 2 sites in 2 countries.

Detailed Summary

Hereditary angioedema ("HAE") is a genetic disorder characterized by sudden recurrent attacks of local swelling (angioedema). These attacks are often painful and disabling, and, in some cases, life-threatening. "HAE" is caused by mutations in the "C1INH" gene that leads to a decrease in the blood level of functional "C1INH". This multi-center study was designed to assess the safety and tolerability, efficacy and pharmacodynamics/ pharmacokinetics of recombinant human C1 inhibitor ("rhC1INH") in the treatment of acute hereditary angioedema attacks.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesNetherlands, Romania
Collaborators--

Timeline

Phase 3CompletedFinished
200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedDec 6, 2005
Enrollment StartJun 1, 2004
Primary CompletionJul 1, 2009
Study CompletionOct 1, 2009
TodayJul 2, 2026
Enrollment to primary: 5.1 yearsPosted 20.6 years ago

Interventions

recombinant human C1 inhibitordrug

IV

Placebodrug

IV