2018│2017
September 20, 2018
Health Canada has authorized TAKHZYROTM (lanadelumab injection), a first-of-its- kind monoclonal antibody treatment for the prevention of hereditary angioedema (HAE) attacks
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June 21, 2018
Shire Announces FDA Approval for Label Expansion of CINRYZE® (C1 esterase inhibitor [human]) for Prevention of Attacks in Pediatric Hereditary Angioedema Patients
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May 16, 2018
KalVista Pharmaceuticals Recognizes HAE Day
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April 9, 2018
HAEA comments on ICER HAE therapy assessment
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February 25, 2018
FDA Accepts Shire’s Biologics License Application (BLA) and Grants Priority Review for Lanadelumab for the Prevention of Attacks in Hereditary Angioedema (HAE) Patients
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February 15, 2018
Shire Announces FDA Acceptance of sBLA for CINRYZE® (C1 esterase inhibitor [human]) for Pediatric Hereditary Angioedema Use
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January 24, 2018
FDA Grants Approval to Shire for Technology Transfer of CINRYZE® (C1 esterase inhibitor [human]) Drug Product Manufacturing Process to Vienna, Austria Manufacturing Site
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January 22, 2018
BioCryst Pharmaceuticals and Idera Pharmaceuticals Announce Merger to Combine Capabilities to Serve More Patients with Rare Diseases
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January 8, 2018
A Big Pharma-funded charity that helps patients pay for drugs just sued the government
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January 5, 2018
KalVista Pharmaceuticals Commences Two Clinical Trials
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September 29, 2017
RUCONEST® provided clinically meaningful relief of symptoms in children with hereditary angioedema
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September 14, 2017
KalVista Pharmaceuticals Reports Fiscal First Quarter Results
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September 11, 2017
Shire’s Investigational Subcutaneous C1 esterase inhibitor (C1 INH [Human]) Liquid for Injection (SHP616) Significantly Reduces Hereditary Angioedema Monthly Attack Rate Versus Placebo in a Phase 3 Pivotal Trial
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September 11, 2017
Pharming announces conclusion of FDA End of Phase 2 interactions on RUCONEST® for Prophylaxis of HAE
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September 5, 2017
BioCryst Announces Positive Results from its APeX-1 Phase 2 Trial in HAE
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July 26, 2017
Pharming announces publication of RUCONEST® prophylactic data in The Lancet
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July 23, 2017
FDA Approves HAEGARDA® King Of Prussia, PA
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June 22, 2017
FDA Approves First Subcutaneous C1 Esterase Inhibitor To Treat Rare Genetic Disease
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May 24, 2017
Attune Pharmaceuticals Announces Positive Data from Recent Pre-Clinical Studies for ATN-249, an Oral Plasma Kallikrein Inhibitor for the Treatment of HAE at C1-INH Deficiency Workshop
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May 24, 2017
Shire’s Investigational Treatment Lanadelumab Reduces Hereditary Angioedema Monthly Attack Rate by 87% Versus Placebo in Phase 3 26-week Pivotal Trial
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April 13, 2017
BioCryst Expands Development of BCX7353 to Explore Treatment of Acute HAE Attacks
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March 23, 2017
New England Journal of Medicine Publishes Pivotal Phase III Data for CSL Behring’s Subcutaneous C1-Esterase Inhibitor in HAE Patients
