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NCT00004474

Phase III Randomized Study of Cyclophosphamide With or Without Antithymocyte Globulin Before Bone Marrow Transplantation in Patients With Aplastic Anemia

Completed Phase 3 Last updated 9 March 2018
What this trial tests

Phase 3 trial testing Anti-thymocyte globulin in Aplastic Anemia in 224 participants. Completed in 1 August 2007.

Timeline
1 September 1998
Primary endpoint
1 August 2007
1 August 2007

Quick facts

Lead sponsorRoswell Park Cancer Institute
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Primary purposetreatment
Enrollment224
Start date1 September 1998
Primary completion1 August 2007
Estimated completion1 August 2007
Sites4 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Roswell Park Cancer Institute

Who can join

Under 59, any sex, with Aplastic Anemia. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

OBJECTIVES: I. Compare outcome, including graft failure, graft versus host disease, and survival of HLA-identical sibling bone marrow transplants for aplastic anemia using cyclophosphamide with or without antithymocyte globulin as a conditioning regimen.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Anti-thymocyte globulin

Trials testing the same drug.

Other recruiting trials for Aplastic Anemia

Currently open trials in the same condition.

Other Roswell Park Cancer Institute trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00004474.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing