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Hereditary Angioedema clinical trials

View clinical trials related to Hereditary Angioedema.

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NCT ID: NCT00914966 Completed - Clinical trials for Hereditary Angioedema

A Study to Evaluate the Safety and Effect of Escalating Doses of CINRYZE

Start date: August 31, 2009
Phase: Phase 4
Study type: Interventional

The objectives of the study were: 1. To assess the safety and tolerability of escalating doses of CINRYZE. 2. To assess the effect of an escalating dose algorithm for CINRYZE on hereditary angioedema (HAE) attack rates. 3. To assess the immunogenicity of CINRYZE.

NCT ID: NCT00912093 Completed - Clinical trials for Hereditary Angioedema

A Study of Icatibant in Patients With Acute Attacks of Hereditary Angioedema (FAST-3)

Start date: July 16, 2009
Phase: Phase 3
Study type: Interventional

This study is being conducted to evaluate the efficacy and safety of icatibant compared to placebo in patients experiencing acute attacks of hereditary angioedema (HAE).

NCT ID: NCT00851409 Completed - Clinical trials for Hereditary Angioedema

A Study of the Safety and Immunogenicity of Repeated rhC1INH Administration

OPERA
Start date: June 2009
Phase: Phase 2
Study type: Interventional

Hereditary angioedema ("HAE") is a disease characterized by recurrent tissue swelling affecting various body locations. Recent literature shows that patients with frequent attacks may benefit from long-term prophylaxis. This study aims to evaluate the safety and prophylactic effect of weekly administrations of 50 IU/kg recombinant C1 Inhibitor ("rhC1INH").

NCT ID: NCT00748202 Completed - Clinical trials for Hereditary Angioedema

Berinert P Study of Subcutaneous Versus Intravenous Administration

PASSION
Start date: September 2008
Phase: Phase 3
Study type: Interventional

The study is performed to investigate the subcutaneous (s.c.) versus intravenous (i.v.) administration of Berinert P in patients with hereditary angioedema (HAE) to establish a second administration mode in cases where i.v. access is not suitable. The study is planned as a single centre, randomized, open-label, cross-over pharmacokinetic study. Subjects will either start with s.c. or i.v. pasteurised C1-Inhibitor concentrate (Berinert P) and than switch to the treatment not administered before.

NCT ID: NCT00500656 Completed - Clinical trials for Hereditary Angioedema

Subcutaneous Treatment With Icatibant for Acute Attacks of Hereditary Angioedema (HAE)

FAST2
Start date: March 1, 2005
Phase: Phase 3
Study type: Interventional

Primary Outcome Measures: The primary endpoint was the time to onset of symptom relief of the first attack in the double blind phase. H0: λ icatibant/λ tranexamic acid =1 versus H1: λ icatibant/λ tranexamic acid ≠1 Where: λ icatibant refers to the hazard rate under icatibant and λ tranexamic acid refers to the hazard rate under tranexamic acid. Secondary Outcome Measures: - Additional efficacy assessments (Time to Almost Complete Symptom Relief) - Safety and tolerability - Pharmacoeconomics

NCT ID: NCT00462709 Completed - Clinical trials for Hereditary Angioedema

Open-Label C1 Esterase Inhibitor (C1INH-nf) for the Prevention of Acute Hereditary Angioedema (HAE) Attacks

CHANGE 3
Start date: June 27, 2006
Phase: Phase 3
Study type: Interventional

The study objective was to evaluate the safety and efficacy of prophylactic use of C1INH-nf for the prevention of acute HAE attacks.

NCT ID: NCT00438815 Completed - Clinical trials for Hereditary Angioedema

Open-Label C1 Esterase Inhibitor (C1INH-nf) for the Treatment of Acute Hereditary Angioedema (HAE) Attacks

CHANGE 2
Start date: September 21, 2006
Phase: Phase 3
Study type: Interventional

The study objective was to evaluate the safety and efficacy of repeat use of C1INH-nf for the treatment of acute HAE attacks.

NCT ID: NCT00432510 Completed - Clinical trials for Hereditary Angioedema

Pharmacokinetics of C1 Esterase Inhibitor in Hereditary Angioedema Subjects

Start date: October 9, 2006
Phase: Phase 1
Study type: Interventional

The study objective was to describe the pharmacokinetics (PK) of one or two doses of C1 esterase inhibitor (C1INH-nf) in hereditary angioedema (HAE) subjects who were not experiencing an HAE attack.

NCT ID: NCT00292981 Completed - Clinical trials for Hereditary Angioedema

C1 Esterase Inhibitor in Hereditary Angioedema (HAE)(Extension Study)

Start date: August 2005
Phase: Phase 3
Study type: Interventional

Hereditary angioedema (HAE) is a rare disorder characterized by congenital lack of functional C1 esterase inhibitor. If not treated adequately, the acute attacks of HAE can be life-threatening and may even result in fatalities, especially in case of involvement of the larynx.The planned extension study is designed to enrol subjects that participated in the pivotal study in order to provide them with C1-INH for treatment of acute HAE attacks for 24 months or until the licensing procedure for C1-INH is finalized, whatever comes first.

NCT ID: NCT00289211 Completed - Clinical trials for Hereditary Angioedema

C1 Esterase Inhibitor (C1INH-nf) for the Treatment of Acute Hereditary Angioedema (HAE) Attacks

Start date: March 14, 2005
Phase: Phase 3
Study type: Interventional

The study objective was to determine the safety and efficacy of C1INH-nf for the treatment of acute HAE attacks.