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Clinical Trials/NCT04970004
NCT04970004
Withdrawn
N/A

A Retrospective Observational Study of Adult and Pediatric Patients With Thrombotic Microangiopathy (TMA) After Hematopoietic Stem Cell Transplant (HSCT)

Alexion Pharmaceuticals, Inc.1 site in 1 countryJuly 12, 2021

Overview

Phase
N/A
Intervention
Not specified
Conditions
Stem Cell Transplant Complications
Sponsor
Alexion Pharmaceuticals, Inc.
Locations
1
Primary Endpoint
Proportion of patients achieving TMA Response
Status
Withdrawn
Last Updated
3 years ago

Overview

Brief Summary

This is an observational, retrospective study designed to assess outcomes in patients diagnosed with hematopoietic stem cell transplant-associated thrombotic microangiopathy (HSCT-TMA) who were not treated with complement component (C5) inhibitor therapy. Data required to evaluate study outcomes will be abstracted from the medical records of all patients who meet study eligibility criteria.

Registry
clinicaltrials.gov
Start Date
July 12, 2021
End Date
April 1, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Body weight ≥ 5 kg at the time of HSCT-TMA diagnosis
  • Documented TMA diagnosis within 6 months from the HSCT
  • Evidence of renal dysfunction
  • Presence of hypertension

Exclusion Criteria

  • History or presence of familial or acquired 'a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13' (ADAMTS13) deficiency (activity \< 5%)
  • Shiga toxin-related hemolytic uremic syndrome (ST-HUS)
  • Positive direct Coombs test
  • Diagnosis of disseminated intravascular coagulation
  • History or presence of bone marrow/graft failure
  • Diagnosis of veno-occlusive disease
  • Received a complement inhibitor (eg, eculizumab) post-HSCT through 12 months post TMA diagnosis

Outcomes

Primary Outcomes

Proportion of patients achieving TMA Response

Time Frame: During the 26-week period after HSCT-TMA diagnosis

TMA Response is defined as platelet count ≥ 50,000/mm\^3, lactate dehydrogenase \< 1.5 upper limit of normal, absence of schistocytes (if present at baseline), and increase in eGFR ≥ 30% from baseline or discontinuation of dialysis (for patients on dialysis at baseline)

Secondary Outcomes

  • Proportion of patients achieving TMA response(During the 52-week period after HSCT-TMA diagnosis)
  • Changes in individual components of TMA response(From baseline to 26 weeks and to 52 weeks after HSCT-TMA diagnosis)
  • Overall survival(At 26 weeks and 52 weeks after HSCT-TMA diagnosis)
  • Nonrelapse mortality(At 26 weeks and 52 weeks after HSCT-TMA diagnosis)

Study Sites (1)

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