Hereditary Angioedema: Clinical Trials

16 trials for Hereditary Angioedema, newest first

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16 completed. 16 Phase 2, 4 Phase 3, 1 Phase 1.

By phase and status

PhaseTrialsStatus
Phase 216Completed 16
Phase 34Completed 4
Phase 11Completed 1

Follow Hereditary Angioedema: new trials by email Literature Review of Hereditary Angioedema trials Research Report on Hereditary Angioedema

Trials (filtered) newest first · largest first

All 16 trials

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
A Study of Navenibart (STAR-0215) in Participants With Hereditary Angioedema
Navenibart - Hereditary Angioedema
Phase 1 / Phase 2CompletedAstria Therapeutics, Inc.292023-02-212026-05-08
Dose-ranging Study of Oral PHA-022121 for Acute Treatment of Angioedema Attacks in Patients With Hereditary Angioedema
Deucrictibant, Placebo - Hereditary Angioedema, Hereditary Angioedema Type I
Phase 2CompletedPharvaris Netherlands B.V.742021-02-032025-12-17
An Extension Study of Donidalorsen (IONIS-PKK-LRx) in Participants With Hereditary Angioedema
Donidalorsen - Hereditary Angioedema
Phase 2CompletedIonis Pharmaceuticals, Inc.202020-03-312026-05-08
A Study to Assess the Clinical Efficacy of Donidalorsen (Also Known as IONIS-PKK-LRx and ISIS 721744) in Participants With Hereditary Angioedema
Donidalorsen, Placebo - Hereditary Angioedema
Phase 2CompletedIonis Pharmaceuticals, Inc.232020-01-072023-04-03
A Phase II, Cross-over Clinical Trial Evaluating the Efficacy and Safety of KVD900 (Sebetralstat) in the On-demand Treatment of Angioedema Attacks in Adult Subjects With Hereditary Angioedema Type I or II
KVD900, Placebo - Hereditary Angioedema
Phase 2CompletedKalVista Pharmaceuticals, Ltd.842019-07-022025-05-02
A Study to Investigate CSL312 in Subjects With Hereditary Angioedema (HAE)
Factor XIIa antagonist monoclonal antibody, Placebo - Hereditary Angioedema
Phase 2CompletedCSL Behring442018-10-292022-11-08
A Long Term Safety Study of BCX7353 in Hereditary Angioedema
BCX7353 - Hereditary Angioedema, HAE
Phase 2 / Phase 3CompletedBioCryst Pharmaceuticals3872018-02-162023-06-18
12-Week Safety and Efficacy Study of BCX4161 as an Oral Prophylaxis Against HAE Attacks
BCX4161, Placebo - Hereditary Angioedema, HAE
Phase 2 / Phase 3CompletedBioCryst Pharmaceuticals1102014-12-172025-11-17
A Phase 2 HAE Prophylaxis Study With Recombinant Human C1 Inhibitor
Recombinant human C1 inhibitor, Placebo - Hereditary Angioedema
Phase 2CompletedPharming Technologies B.V.322014-12-012017-12-08
Safety and Efficacy of Oral BCX4161 as a Prophylactic Treatment for HAE
BCX4161, Placebo - Hereditary Angioedema
Phase 2CompletedBioCryst Pharmaceuticals242013-11-012014-08-18
Safety of Ruconest in 2-13 Year Old Hereditary Angioedema (HAE) Patients
rhC1INH - Hereditary Angioedema
Phase 2CompletedPharming Technologies B.V.572012-01-172024-03-29
A Study to Evaluate the Safety and Pharmacology of Subcutaneous Administration of CINRYZE With Recombinant Human Hyaluronidase
CINRYZE with rHuPH20 - Hereditary Angioedema
Phase 2CompletedShire122011-09-122021-07-19
A Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Subcutaneous CINRYZE Administration
CINRYZE - Hereditary Angioedema
Phase 2CompletedShire262010-06-072021-07-09
A Study of the Safety and Immunogenicity of Repeated rhC1INH Administration
Recombinant Human C1 Inhibitor - Genetic Disorders, Hereditary Angioedema
Phase 2CompletedPharming Technologies B.V.252009-06-012018-06-26
Recombinant Human C1 Inhibitor for the Treatment of Acute Attacks in Patients With Hereditary Angioedema
Recombinant Human C1 Inhibitor, placebo - Hereditary Angioedema, Angioneurotic Edema
Phase 2 / Phase 3CompletedPharming Technologies B.V.772005-07-012013-02-22
Human C1 Esterase Inhibitor (C1-INH) in Subjects With Acute Abdominal or Facial Hereditary Angioedema (HAE) Attacks
C1 Esterase Inhibitor, Placebo - Hereditary Angioedema
Phase 2 / Phase 3CompletedCSL Behring1262005-06-012015-03-31

Narrower conditions

Angioedemas, Hereditary (16)  ·  Angioedema (3)  ·  Genetic Diseases, Inborn (1)  ·  Hereditary Angioedema Types I and II (1)

Broader conditions

Cardiovascular Diseases (16)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (16)  ·  Hereditary Complement Deficiency Diseases (16)  ·  Hypersensitivity (16)  ·  Hypersensitivity, Immediate (16)  ·  Immune System Diseases (16)  ·  Immunologic Deficiency Syndromes (16)  ·  Primary Immunodeficiency Diseases (16)  ·  Skin Diseases (16)  ·  Skin Diseases, Vascular (16)  ·  Skin and Connective Tissue Diseases (16)  ·  Urticaria (16)  ·  Vascular Diseases (16)  ·  Genetic Diseases, Inborn (15)  ·  Angioedema (13)

Interventions

Complement C1 Inhibitor Protein (5)  ·  conestat alfa (4)  ·  IONIS-PKK-LRx (2)  ·  SERPING1 protein, human (2)  ·  Sodium Chloride (2)  ·  avoralstat (2)  ·  donidalorsen (2)  ·  berotralstat (1)  ·  sebetralstat (1)

Sponsors

Pharming Technologies B.V. (4)  ·  BioCryst Pharmaceuticals (3)  ·  CSL Behring (2)  ·  Ionis Pharmaceuticals, Inc. (2)  ·  Shire (2)  ·  Astria Therapeutics, Inc. (1)  ·  KalVista Pharmaceuticals, Ltd. (1)  ·  Pharvaris Netherlands B.V. (1)

Countries

United States (13)  ·  Germany (8)  ·  United Kingdom (7)  ·  Canada (6)  ·  Czechia (6)  ·  Hungary (6)  ·  Italy (6)  ·  Netherlands (6)  ·  Israel (5)  ·  North Macedonia (5)  ·  Poland (5)  ·  Romania (4)  ·  Australia (3)  ·  Bulgaria (3)  ·  France (3)

Top investigators

Anurag Relan, MD (2)  ·  Bruno Giannetti, MD (1)  ·  Henriette Farkas, MD (1)  ·  Marc Riedl, MD MS (1)  ·  Marcus Maurer, MD (1)  ·  Marcus Maurer, Prof MD (1)

Results publications

PMID 36326435, PMID 19767078, PMID 20674826, PMID 20920772, PMID 23535096, PMID 23987198, PMID 28284978, PMID 28754491, PMID 30993784, PMID 34161665, PMID 35219377, PMID 35294812, PMID 35820771, PMID 36408587, PMID 36774155, PMID 38006972, PMID 38009241, PMID 38020288, PMID 38710185, PMID 40490218, PMID 41794053, PMID 41802598, PMID 41865747, PMID 42159953, PMID 42268494, PMID 42318595

NIH funding

2004 (1), 2018 (1), 2019 (1)