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- Klinische proef NCT07705789
The Role of interferOn and Complement in SecondAry thRombotic micrioangiOpathy (ROSARIO)
The Role of interferOn and Complement in SecondAry thRombotic micrioangiOpathy (ROSARIO)
Study rationale: Viral infections, such as CMV, are a risk factor for TA-TMA (transplantation-associated TMA). Viral infections increase interferon (IFN) levels and high IFN levels are associated with thrombotic microangiopathy (TMA). IFNs contribute to TMA pathogenesis through suppression of VEGF transcription. Disruption of the VEGF signalling pathway in the kidney is associated with TMA.
Primary objective: To determine the association between IFN levels and the development of biopsy-proven or clinically diagnosed TA-TMA.
Secondary objective(s): To explore the relationship between complement activation and IFN in patients with TMA.
To explore if high IFN levels are associated with low VEGF-A levels. Endpoint: The study aims to investigate the role of IFN in the pathogenesis of secondary thrombotic microangiopathy (focusing on patients with TA-TMA). It seeks to clarify whether IFN, next to complement dysregulation, is a driver of endothelial damage and TMA in these patients.
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Studietype
Inschrijving (Geschat)
Fase
- Niet toepasbaar
Contacten en locaties
Studiecontact
- Naam: Sofie A Dhaese, MD, PhD
- Telefoonnummer: +320050452200
- E-mail: sofie.dhaese@azsintjan.be
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria:
Participants eligible for inclusion in this study must meet all of the following criteria:
- Voluntary written informed consent of the participant or their legally authorized representative has been obtained prior to any screening procedures
- At least 18 years of age at the time of signing the Informed Consent Form (ICF)
Specifically for the patients with TMA (G1 and G4):
- Patients after allogeneic or autologous hematopoietic stem cell transplantation (HSCT) OR patients after solid organ transplantation OR patients with DITMA AND
- Tissue diagnosis of TMA (pathological diagnosis) OR
Clinical diagnosis of TMA based on the following criteria, with ≥4 out of 6 features fulfilled within 14 days (15,52,53):
de novo Coombs negative hemolytic anemia OR (in case of HSCT)
- failure to achieve transfusion independence despite neutrophil engraftment
- hemoglobin decline by ≥ 1g/dL
- new onset transfusion dependence
otherwise unexplained de novo thrombocytopenia (< 50 x 109/L) OR a 25% decrease in platelet count OR (in case of HSCT)
- failure to achieve platelet engraftment despite neutrophil engraftment
- higher than expected transfusion needs
- refractory to platelet transfusion *≥50% reduction in platelet count after full platelet engraftment
- lactate dehydrogenase (LDH) above the upper limit of normal
- schistocytes (=>2 / high power field (HPF)
- new onset hypertension OR worsening of existing hypertension requiring additional antihypertensive therapy
- proteinuria > 1g/g creatinine on a random urine protein-to-creatinine ratio Date of TMA diagnosis = first date when ≥4 out of the 6 features are fulfilled.
Specifically for the group of patients without TMA, with infection (G2):
- Patients after allogeneic or autologous hematopoietic stem cell transplantation (HSCT) OR patients after solid organ transplantation AND
- Symptomatic viral infection (evaluated by the treating physician).
Specifically for the group of patients without TMA, without infection (G3):
- Patients after allogeneic or autologous hematopoietic stem cell transplantation (HSCT) OR patients after solid organ transplantation AND
- No symptomatic viral infection (evaluated by the treating physician).
Exclusion Criteria:
Participants eligible for this study must not meet any of the following criteria:
- Participant has a personal or family history of aHUS
- Participant has a history of malignant hypertension
- Participant has a history of active cancer, excluding the haematological cancer for which the patient received the stem cell transplantation (if applicable)
- The participant received prior complement inhibition
- The participant received prior anti-interferon treatment
- If applicable: Female who is pregnant, breast-feeding or intends to become pregnant the following year or is of child-bearing potential and not using an adequate, highly effective contraceptive
- Participation in an interventional study with an investigational medicinal product (IMP) or device
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: NVT
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Ander: Patients with HSCT-TMA or SOT-TMA
blood and urine collection
|
blood sampling at designated time points
urine collection at designated time points
|
|
Ander: Patients after HSCT or SOT with a viral infection, without TMA
blood and urine collection
|
blood sampling at designated time points
urine collection at designated time points
|
|
Ander: Patients after HSCT or SOT without a viral infection, without TMA
blood and urine collection
|
blood sampling at designated time points
urine collection at designated time points
|
|
Ander: Patients with drug-induced TMA (DITMA)
blood and urine collection
|
blood sampling at designated time points
urine collection at designated time points
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Interferon signature
Tijdsspanne: Time point 1: baseline Time point 2: up to week 52
|
6-gene interferon signature
|
Time point 1: baseline Time point 2: up to week 52
|
|
VEGF-A
Tijdsspanne: Time point 1: baseline Time point 2: up to week 52
|
VEGF-A level
|
Time point 1: baseline Time point 2: up to week 52
|
|
Complement analysis (serum)
Tijdsspanne: Time point 1: baseline Time point 2: up to week 52
|
CH50, AP50, C3, C3d, C4 and C5b-9 at timepoint 1 and C5b-9 at time point 2
|
Time point 1: baseline Time point 2: up to week 52
|
Medewerkers en onderzoekers
Sponsor
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Cytopenie
- Hematologische ziekten
- Bloedplaatjesstoornissen
- Trombocytopenie
- Hemische en lymfatische ziekten
- Trombotische microangiopathieën
- Onderzoekstechnieken
- Exemplaarbehandeling
- Klinische laboratoriumtechnieken
- Diagnostische technieken en procedures
- Diagnose
- Buren
- Chirurgische procedures, operatief
- Bloedspecimenverzameling
- Urine -specimencollectie
Andere studie-ID-nummers
- ROSARIO
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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