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Thymosin Alfa 1 in Recipients of Allogeneic Hematopoietic Transplantation for Hematological Malignancies

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Contents

clinicaltrials.gov/study/NCT00580450
Is a
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Clinical study
0

Clinical Study attributes

NCT Number
NCT005804500
Trial Recruitment Size
90
Trial Sponsor
University of Perugia
University of Perugia
0
Clinical Trial Start Date
2007
0
Primary Completion Date
2007
0
Study Completion Date
2010
0
Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Treatment0
Intervention Type
Drug0
Interventional Trial Phase
Phase 20
Phase 10
Official Name
Phase I/II Clinical Trial on Thymosin Alfa 1 of Allogeneic Hematopoietic Transplantation0
Last Updated
December 24, 2007
0
Allocation Type
Randomized0
Intervention Model
Parallel Assignment0
Masking Type
None (Open Label)0

Other attributes

Intervention Treatment
Thymosin alpha 10
Study summary

The purpose of this trial is to determine safety and efficacy of 16 weeks treatment with thymosin alpha 1 given at 1.6 mg dose once daily by subcutaneous injection in adult patients with hematological undergone allogenic bone marrow transplantation and CMV positive. The efficacy will be explored assessing the ability of thymosin alpha1 to prevent the infection complications.

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