Clinical Trials Directory

Trials / Completed

CompletedNCT01397864

C1 Inhibitor Registry in the Treatment of Hereditary Angioedema (HAE) Attacks

C1 Inhibitor Treatment Registry to Assess the Safety and Immunological Profile of Ruconest in the Treatment of HAE Attacks

Status
Completed
Phase
Study type
Observational
Enrollment
181 (actual)
Sponsor
Pharming Technologies B.V. · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

This is a non-interventional treatment Registry of Hereditary Angioedema (HAE) patients treated with C1 inhibitor, either plasma-derived (pdC1INH) or the recombinant human form (rhC1INH / Ruconest), to observe adverse events and insufficient efficacy, and to assess the immunological profile following single and repeated treatment with Ruconest.

Detailed description

see below

Conditions

Interventions

TypeNameDescription
DRUGrhC1INH or pdC1INHC1 inhibitor, either plasma-derived (pdC1INH) or the recombinant human form (Ruconest)

Timeline

Start date
2011-07-01
Primary completion
2024-10-18
Completion
2024-12-10
First posted
2011-07-20
Last updated
2025-04-08

Locations

17 sites across 13 countries: Bulgaria, Croatia, Czechia, France, Germany, Hungary, Italy, North Macedonia, Norway, Poland, Slovakia, Slovenia, Sweden

Source: ClinicalTrials.gov record NCT01397864. Inclusion in this directory is not an endorsement.