Hereditary angioedema (HAE) research hub
13 indexed studies · 5 currently recruiting
- ongoing, recruitingTherapeutic confirmatory (Phase III)
A Phase 3 Open-label Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Efficacy of CSL312 (Garadacimab) in the Prophylactic Treatment of Hereditary Angioedema in Pediatric Subjects 2 to 11 Years of Age
This study is testing a new medicine, garadacimab, for children aged 2-11 with hereditary angioedema (HAE). It aims to see how safe the medicine is, how it moves through the body, and if it helps prevent HAE attacks. Researchers will also check for any side effects.
Germany · Italy - ongoing, recruitingHuman Pharmacology (Phase I)- Other
A Phase I, open-label, randomized, two period, cross-over study in healthy subjects to assess the bioavailability of different formulations of deucrictibant administered as single dose under fasting condition.
This study is looking at how well different versions of a new medicine for hereditary angioedema (HAE) are absorbed by the body. Healthy volunteers will take a single dose of the medicine and have their blood checked. We want to find the best way to give this new treatment.
Hungary - active not recruiting
A Study of Lanadelumab in Teenagers and Adults With Hereditary Angioedema (HAE)
This study looks at how a medicine called lanadelumab helps teenagers and adults in the UK with a swelling condition called Hereditary Angioedema (HAE). We're comparing their HAE attacks before and after starting this treatment to see how well it works.
United Kingdom - recruitingPHASE3
Long-Term, Open-label Study of Oral Deucrictibant Extended-Release Tablet for Prophylaxis Against Angioedema Attacks in Adolescents and Adults With HAE
This study is looking at a new tablet, deucrictibant, for teenagers and adults with Hereditary Angioedema (HAE). It aims to see if taking it daily can safely and effectively reduce painful swelling attacks over a long period.
United States · Argentina · Australia - enrolling by invitationPHASE2, PHASE3
Extension Study of Oral PHA-022121 for Acute Treatment of Angioedema Attacks in Patients With Hereditary Angioedema
This study looks at a new daily medicine called deucrictibant for people aged 12 and over with hereditary angioedema (HAE). It's for long-term use to treat sudden swelling attacks, including dangerous swelling in the throat. Researchers want to see how safe and effective it is over time.
United States · Argentina · Australia - ongoing, recruitingTherapeutic use (Phase IV)
A phase 4 open-label study to evaluate the safety after switching to CSL312 (Garadacimab) from current prophylactic HAE treatment in subjects with HAE ≥ 12 years of age
This study looks at the safety of switching to a new medication called garadacimab for people aged 12 and over with Hereditary Angioedema (HAE). It aims to see how common side effects are after making the switch from their usual treatment.
Germany - enrolling by invitationPHASE3
A Long-Term Study of Navenibart in Participants With Hereditary Angioedema
This study looks at a new medicine called navenibart for people with hereditary angioedema (HAE). It checks how safe and effective it is over a long time. Only people who were in a previous study with this medicine can join.
United States · Brazil · Bulgaria - active not recruitingPHASE3
Study of Oral Deucrictibant Extended-Release Tablet for Prophylaxis Against Angioedema Attacks in Adolescents and Adults With HAE
This study is looking at a new tablet, deucrictibant, to see if it can help prevent swelling attacks in people with Hereditary Angioedema (HAE). It includes adults and children aged 12 and over, comparing the new drug to a dummy pill (placebo).
United States · Argentina · Brazil - active not recruitingPHASE3
A Study of Navenibart in Participants With Hereditary Angioedema
This study is testing a new medicine, navenibart, for people with Hereditary Angioedema (HAE). Researchers want to see if it safely and effectively prevents swelling attacks in adults and teenagers with HAE.
United States · Australia · Austria - recruiting
A Study of Lanadelumab in Children With Hereditary Angioedema (HAE) in Multiple Countries
This study looks at how well a medicine called lanadelumab (Takhzyro) works for children aged 2-11 with a rare swelling condition called Hereditary Angioedema (HAE). We're checking how long children go without swelling attacks when taking this medicine in their daily lives, using existing medical records.
Argentina · France · Germany - ongoing, recruitingHuman Pharmacology (Phase I)- Other
A Phase I, Open-Label, Randomized, Two-Period, Cross-Over Study in Healthy Subjects to Assess the Influence of a High-Calorie, High-Fat Meal on the Bioavailability of a 40 mg Extended-Release (XR) Deucrictibant Oral Formulation Administered as a Single Dose.
This study is looking at how a new medicine, deucrictibant, is absorbed by the body. We're testing if eating a big, fatty meal changes how much of the medicine gets into your system when you take it as an extended-release tablet in healthy people.
Hungary - recruitingPHASE3
Phase 3 Extension Study of ADX-324 in Participants With Hereditary Angioedema (HAE)
This study is an extension of a previous trial for people with a condition called hereditary angioedema (HAE). It's looking at the long-term safety and how well a medicine, ADX-324, works for HAE types 1 and 2. Participants would have already taken part in the earlier study.
United States · Argentina · Australia - ongoing, recruitingPhase I and Phase II (Integrated)- Other
A Phase 1b/2 Single and Multiple Dose Study to Assess the Safety, Tolerability, Clinical Activity, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of STAR-0215 in Participants with Hereditary Angioedema (The ALPHA-STAR Trial)
This study is testing a new medicine called STAR-0215 for people with Hereditary Angioedema (HAE). We want to check if it's safe, how much your body handles, and if it helps reduce swelling attacks. It's an early-stage study to understand the medicine better.
Czechia · Poland · Bulgaria