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|a (UBBS_Klinische_Studien_WHO)EUCTR2017-000348-17-GB
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|a (UBBS_Klinische_Studien_WHO)CSL842_3001
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|a (UBBS_Klinische_Studien_WHO)2017-000348-17-BE
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|a Efficacy and safety of human plasma-derived C1-esterase inhibitor as add-on to standard of care for the treatment of refractory antibody mediated rejection (AMR) in adult renal transplant recipients
|b A Double-blind, Randomized-Withdrawal, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Human Plasma-Derived C1-esterase Inhibitor as Add-on to Standard of Care for the Treatment of Refractory Antibody Mediated Rejection in Adult Renal Transplant Recipients
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|a WHO International Clinical Trials Registry Platform (https://www.who.int/ictrp/en/), First posted: 12-05-2017, Last updated: 2023-06-29
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|a Medical Condition: Refractory AMR in adult renal transplant participants MedDRA version: 20.0Level: PTClassification code 10023439Term: Kidney transplant rejectionSystem Organ Class: 10021428 - Immune system disorders;Therapeutic area: Body processes [G] - Immune system processes [G12]
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|a Study Type: Interventional
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|a Phase: Phase 3
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|a Recruitment Status: Authorised-recruitment may be ongoing or finished
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Klinische Studie