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Active clinical trials for "Angioedemas, Hereditary"

Results 31-40 of 134

A Study of Lanadelumab in Persons With Hereditary Angioedema (HAE) Type I or II

Hereditary Angioedema (HAE)

The main aim of this study is to compare the number of HAE attacks occuring in persons using lanadelumab with the number of HAE attacks before lanadelumab treatment was started. Data from participants who start the study after 1 March 2021, will be collected for 24 months; data from all other participants (who started the study before 1 March 2021) will be collected for 36 months. Participants will report information in a smartphone application at study start and for the next 3 months and then every 6 months until the study ends; data will also be collected by the study doctor during routine clinic visits

Active10 enrollment criteria

C1-inhibitor in Allergic ASThma Patients

Asthma

The purpose of this proof-of-concept study is to determine the effect of Intestinal Microbiota Depletion or Intravenous Administration of C1-inhibitor on Inflammation and Coagulation after Bronchial Instillation of House Dust Mite Allergen and Lipopolysaccharide in Allergic Asthma Patients

Terminated18 enrollment criteria

A Phase II, Cross-over Clinical Trial Evaluating the Efficacy and Safety of KVD900 in the On-demand...

Hereditary Angioedema

This study is a randomized, double-blind, placebo-controlled, phase II, cross-over clinical trial evaluating the efficacy and safety of KVD900, in the treatment of hereditary angioedema attacks in adult subjects.

Completed23 enrollment criteria

A Study to Assess the Clinical Efficacy of Donidalorsen (Also Known as IONIS-PKK-LRx and ISIS 721744)...

Hereditary Angioedema

The purpose of this study was to evaluate the clinical efficacy, safety, and tolerability of donidalorsen in participants with hereditary angioedema (HAE) type 1 (HAE-1), HAE type 2 (HAE-2), or HAE with normal C1-inhibitor (C1-INH) and to evaluate the effect of donidalorsen on plasma prekallikrein (PKK) and other relevant biomarkers.

Completed12 enrollment criteria

Open-label, Single-arm Study to Assess the Pharmacokinetics, Safety, and Tolerability of a Single...

Hereditary Angioedema (HAE)

This is a single-dose study to evaluate the pharmacokinetics, safety, and tolerability of icatibant administered to adult Japanese subjects.

Completed11 enrollment criteria

Study to Determine How BCX4161 is Metabolized and Eliminated by the Body

Hereditary Angioedema

The purpose of the study is to assess the extent that radioactive dose of BCX4161 taken by mouth ends up in the urine, feces and expired air. If there are metabolites of BCX4161 made by the body, the chemical composition of these metabolites and their profile over time in blood and urine will be determined.

Completed14 enrollment criteria

A Drug-Drug Interaction Study to Evaluate Drug Transporter Interactions

Hereditary Angioedema

This is an open-label, three part study to evaluate the effect of BCX7353 on drug transporters as well as the effect of an inhibitor of drug transport on BCX7353.

Completed18 enrollment criteria

A Relative Bioavailability Study of Two Formulations of BCX7353

Hereditary Angioedema

This is an open-label, randomized study to investigate the relative bioavailability of two formulations of BCX7353 and to determine if there is a food effect

Completed12 enrollment criteria

Study of C1 Inhibitor (Human) for the Prevention of Angioedema Attacks and Treatment of Breakthrough...

Hereditary Angioedema (HAE)

The purpose of this study is to determine if an investigational treatment is safe and well tolerated when administered by intravenous (IV) infusion in Japanese subjects with HAE.

Completed25 enrollment criteria

A Single Dose Safety, Tolerability, Pharmacokinetic and Food Effect Study of KVD900 in Healthy Volunteers...

Hereditary Angioedema

A safety, tolerability, pharmacokinetic and food effect study of KVD900 in healthy volunteers.

Completed24 enrollment criteria
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