A Study of Lanadelumab to Prevent Hereditary Angioedema (HAE) Attacks in Children

PHASE3CompletedINTERVENTIONAL
Enrollment

21

Participants

Timeline

Start Date

August 19, 2019

Primary Completion Date

October 30, 2021

Study Completion Date

October 30, 2021

Conditions
Hereditary Angioedema
Interventions
DRUG

Lanadelumab

Participants will receive 150 mg dose of lanadelumab every 2 or 4 weeks, depending on the participants age, over the 52-week treatment period.

Trial Locations (17)

1125

Semmelweis Egyetem., Budapest

10029

Icahn School of Medicine at Mount Sinai, New York

10117

Charité - Universitätsmedizin Berlin., Berlin

20815

Institute Asthma and Allergy, Chevy Chase

28046

Hospital Universitario La Paz. Paseo de la Castellana, Madrid

28277

Clinical Research Center of Charlotte, Charlotte

43617

Toledo Institute of Clinical Research Asthma & Allergy Center, Toledo

45231

Bernstein Clinical Research Center, Cincinnati

60590

Klinikum der Johann-Wolfgang Goethe-Universitat., Frankfurt

63110

Washington University School of Medicine, St Louis

64546

Hämophilie Zentrum Rhein Main GmbH, Mörfelden-Walldorf

75231

AARA Research Center, Dallas

80112

IMMUNOe Research Centers, Centennial

90404

AIRE Medical of Los Angeles, Santa Monica

94598

Allergy & Asthma Clinical Research, Walnut Creek

07109

Hudson-Essex Allergy, Belleville

K1G6C6

Yang Medicine, Ottawa

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Shire

INDUSTRY

NCT04070326 - A Study of Lanadelumab to Prevent Hereditary Angioedema (HAE) Attacks in Children | Biotech Hunter | Biotech Hunter