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Trials / Completed

CompletedNCT01283776

Cyclophosphamide as Sole Graft-Versus-Host-Prophylaxis After Allogeneic Stem Cell Transplantation

A Phase II Study to Investigate the Efficacy of Cyclophosphamide as Sole Graft-Versus-Host-Prophylaxis After Allogeneic Stem Cell Transplantation

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
11 (actual)
Sponsor
University of Cologne · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

A phase II clinical study to assess the efficacy of post-transplantation cyclophosphamide as single-agent GvHD prophylaxis after allogeneic hematopoietic stem cell transplantation in patients with multiple myeloma or lymphoma and to describe the influence of the modified immunosuppression concept on relapse rates, minimal residual disease, immune reconstitution and chimerism.

Conditions

Interventions

TypeNameDescription
DRUGCyclophosphamide100 mg/kg total dose, infused on day +3 and +3 after allogeneic stem cell transplantation

Timeline

Start date
2011-03-01
Primary completion
2013-12-01
Completion
2014-06-01
First posted
2011-01-26
Last updated
2014-06-10

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT01283776. Inclusion in this directory is not an endorsement.

Cyclophosphamide as Sole Graft-Versus-Host-Prophylaxis After Allogeneic Stem Cell Transplantation (NCT01283776) · Clinical Trials Directory