Hereditary Angioedema (HAE) (C1 Esterase Inhibitor [C1-INH] Deficiency) is an indication for drug development with over 30 pipeline drugs currently active. According to GlobalData, preregistered drugs for Hereditary Angioedema (HAE) (C1 Esterase Inhibitor [C1-INH] Deficiency) have a 85.71% likelihood of approval (LoA) indication benchmark. GlobalData’s report assesses how phase transition success rate (PTSR) and likelihood of approval (LoA) scores for pipeline drugs in Hereditary Angioedema (HAE) (C1 Esterase Inhibitor [C1-INH] Deficiency) compared to historical benchmarks. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
Hereditary Angioedema (HAE) (C1 Esterase Inhibitor [C1-INH] Deficiency) overview
Hereditary angioedema (HAE) is a rare inherited disease that causes considerable swelling in various body tissues, such as the abdomen or face. Symptoms include severe abdominal pain and cramping, dehydration, diarrhea and shock, hoarse voice, difficulty swallowing,and difficulty breathing. Treatment includes medications such as epinephrine, antihistamines, and corticosteroids.
For a complete picture of PTSR and LoA scores for drugs in Hereditary Angioedema (HAE) (C1 Esterase Inhibitor [C1-INH] Deficiency), buy the report here.
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