A Study to Evaluate the Benefit of RUCONEST® in Subjects Who Experience ADRs Related to IVIG Infusions

PHASE4CompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

June 13, 2018

Primary Completion Date

December 1, 2019

Study Completion Date

March 1, 2020

Conditions
CVI - Common Variable Immunodeficiency
Interventions
BIOLOGICAL

C1-esterase inhibitor [recombinant] (C1-INH-R)

C1-INH-R is FDA approved and indicated for the treatment of acute attacks of angioedema in adolescent and adult patients with Hereditary Angioedema (HAE) as a replacement for low levels of C1-esterase inhibitor or low function of C1-esterase inhibitor

Trial Locations (1)

80112

IMMUNOe Research Centers, Centennial

Sponsors
All Listed Sponsors
lead

IMMUNOe Research Centers

INDUSTRY

NCT03576469 - A Study to Evaluate the Benefit of RUCONEST® in Subjects Who Experience ADRs Related to IVIG Infusions | Biotech Hunter | Biotech Hunter