Press Releases

May 15th, 2020
BioCryst Celebrates HAE Patients with HAE Global Walk

May 4th, 2020
CSL Behring is Committed to Supporting Patients

May 1st, 2020
Pharming to Support Patients Continuity in Care

April 22nd, 2020
Takeda Expands Patient Assistance in the U.S. During COVID-19 Crisis

April 21st, 2020
Pharming reports encouraging results from use of RUCONEST® in COVID-19 patients

April 6th, 2020
Mensaje de la Directora de Salud de la HAEA, Lois Perry

April 6th, 2020
A Message from the Director of HAE Health Lois Perry

April 6th, 2020
GLOBAL PLASMA LEADERS COLLABORATE TO ACCELERATE DEVELOPMENT OF POTENTIAL COVID-19 HYPERIMMUNE THERAPY

March 19th, 2020
An Important Message Regarding HAEA Upcoming Events

March 18th, 2020
How Our Pharmaceutical Companies Are Managing the Coronavirus Situation.

March 6th, 2020
A Message from HAEA Nurse Case Manager Troyce Venturella

January 13th, 2020
KalVista Pharmaceuticals Provides Update on Oral Hereditary Angioedema Franchise

November 27th, 2018
JAMA Publishes Complete Results of Phase 3 HELP Study™ Evaluating Lanadelumab as a Preventive Treatment for Hereditary Angioedema

August 23rd, 2018
Shire Announces FDA Approval of TAKHZYRO™ (lanadelumab-flyo), a First-of-its-Kind mAb Preventive Treatment for Hereditary Angioedema

June 21st, 2018
Shire Announces FDA Approval for Label Expansion of CINRYZE® (C1 esterase inhibitor [human]) for Prevention of Attacks in Pediatric Hereditary Angioedema Patients

May 16th, 2018
KalVista Pharmaceuticals Recognizes HAE Day

April 9th, 2018
HAEA comments on ICER HAE therapy assessment

February 25th, 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

February 15th, 2018
Shire Announces FDA Acceptance of sBLA for CINRYZE® (C1 esterase inhibitor [human]) for Pediatric Hereditary Angioedema Use

January 24th, 2018
FDA Grants Approval to Shire for Technology Transfer of CINRYZE® (C1 esterase inhibitor [human]) Drug Product Manufacturing Process to Vienna, Austria Manufacturing Site

January 22nd, 2018
BioCryst Pharmaceuticals and Idera Pharmaceuticals Announce Merger to Combine Capabilities to Serve More Patients with Rare Diseases

January 8th, 2018
A Big Pharma-funded charity that helps patients pay for drugs just sued the government

January 5th, 2018
KalVista Pharmaceuticals Commences Two Clinical Trials

September 29th, 2017
RUCONEST® provided clinically meaningful relief of symptoms in children with hereditary angioedema

September 14th, 2017
KalVista Pharmaceuticals Reports Fiscal First Quarter Results

September 11th, 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

September 11th, 2017
Pharming announces conclusion of FDA End of Phase 2 interactions on RUCONEST® for Prophylaxis of HAE

September 5th, 2017
BioCryst Announces Positive Results from its APeX-1 Phase 2 Trial in HAE

July 26th, 2017
Pharming announces publication of RUCONEST® prophylactic data in The Lancet

July 23rd, 2017
FDA Approves HAEGARDA® King Of Prussia, PA

June 22nd, 2017
FDA Approves First Subcutaneous C1 Esterase Inhibitor To Treat Rare Genetic Disease

May 24th, 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

May 24th, 2017
Shire's Investigational Treatment Lanadelumab Reduces Hereditary Angioedema Monthly Attack Rate by 87% Versus Placebo in Phase 3 26-week Pivotal Trial

April 13th, 2017
BioCryst Expands Development of BCX7353 to Explore Treatment of Acute HAE Attacks

March 23rd, 2017
New England Journal of Medicine Publishes Pivotal Phase III Data for CSL Behring’s Subcutaneous C1-Esterase Inhibitor in HAE Patients

Ianice Viel
Patient Advocate /
Social Media Manager