Phase
Condition
Vascular Diseases
Treatment
nomacopan (rVA576)
Clinical Study ID
Ages 6-18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Aged ≥ 0.5 and < 18 years at the time of diagnosis of TMA.
Undergone allogeneic or autologous HSCT.
TMA diagnosis within a year of their allogeneic or autologous HSCT.
Clinical or histological diagnosis of TMA
Provision of written informed consent.
Provision of informed assent
Exclusion
Exclusion Criteria:
Patients weighing less than 5 kg.
Patients with a positive direct Coombs' test.
Patients who do not receive nomacopan within 21 days of the initial diagnosis ofTMA.
Patients having an active systemic or organ system bacterial or fungal infection orprogressive severe infection at the time of diagnosis of TMA
Grade 4 Acute graft-versus-host disease (GVHD)
Received eculizumab or any other complement blocker therapy at any time.
Known hypersensitivity to the active ingredient or excipients
If an enrolled patient has a positive ADAMTS13 test (<10%) returned from their screening assessment, the patient should be withdrawn from the study
Study Design
Study Description
Connect with a study center
Uniwersytecki Szpital Kliniczny im. Jana Mikulicza Radeckiego we Wroclawiu
Wrocław, 50556
PolandSite Not Available
Great Ormond Street Hospital (GOSH)
London, WC1N3JH
United KingdomSite Not Available
St. Georges University Hospital
London, SW170QT
United KingdomSite Not Available
The Royal Marsden NHS Foundation Trust
London, SM25PT
United KingdomSite Not Available
Royal Manchester Children's Hospital
Manchester, M139WL
United KingdomSite Not Available
Children's Hospital Los Angeles
Los Angeles, California 90027
United StatesSite Not Available
Stanford Children's Hospital
Palo Alto, California 94304
United StatesSite Not Available
Duke University Medical Center, Children's Health Center
Durham, North Carolina 27710
United StatesSite Not Available
Children's Hospitall of Philadelphia
Philadelphia, Pennsylvania 19104
United StatesSite Not Available

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