Registry Study of Revcovi Treatment in Patients With ADA-SCID

CompletedOBSERVATIONAL
Enrollment

32

Participants

Timeline

Start Date

September 30, 2019

Primary Completion Date

January 18, 2023

Study Completion Date

January 18, 2023

Conditions
Adenosine Deaminase Severe Combined Immunodeficiency
Interventions
BIOLOGICAL

elapegademase-lvlr

Revcovi is administered intramuscularly (i.m.). Weekly dosage is calculated in mg/kg of body weight, and can be adjusted over the course of the trial based on ADA activity and dAXP concentration as well as on clinical assessment by the treating physician.

Trial Locations (14)

14203

UBMD Pediatrics Outpatient Center, Buffalo

15224

UPMC Children's Hospital of Pittsburgh, Pittsburgh

17033

Penn State Children's Hospital, Hershey

20010

Children's National, Washington D.C.

27705

Duke University Hospital, Durham

33701

University of South Florida Allergy Immunology Clinic, St. Petersburg

38105

Le Bonheur Children's Hospital, Memphis

55404

Children's Minnesota, Minneapolis

63110

St. Louis Children's Hospital - Washington University School of Medicine, St Louis

70118

Childrens Hospital of New Orleans, New Orleans

92123

Allergy & Asthma Medical Group and Research Center, A P.C., San Diego

94158

UCSF - University of California, San Francisco

98101

Seattle Children's, Seattle

90095-1752

University of California Los Angeles, Los Angeles

All Listed Sponsors
lead

Chiesi Farmaceutici S.p.A.

INDUSTRY

NCT03878069 - Registry Study of Revcovi Treatment in Patients With ADA-SCID | Biotech Hunter | Biotech Hunter