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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00032773
Other study ID # SGI-NIP-010
Secondary ID NIP-010
Status Terminated
Phase Phase 1/Phase 2
First received
Last updated
Start date January 30, 2002
Est. completion date November 3, 2005

Study information

Verified date October 2020
Source Astex Pharmaceuticals, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To determine a safe and effective dose of pentostatin in steroid-refractory aGvHD and to identify the minimal effective dose of pentostatin defined as the lowest dose that produces a response in 20% or more of patients while producing treatment failure (defines as death, grade 3/4 toxicity, or progressive disease) in 40% or less of patients.


Recruitment information / eligibility

Status Terminated
Enrollment 36
Est. completion date November 3, 2005
Est. primary completion date November 3, 2005
Accepts healthy volunteers No
Gender All
Age group 6 Months and older
Eligibility Inclusion: - Patients 6 months of age with grade 2 GVHD that is steroid-refractory - Must be engrafted with ANC 1000/mL, may still be transfusion dependent for platelets and PRBC - Time post stem cell infusion < 100 days - Written informed consent - Must have adequate renal function (creatinine clearance 40 mL/min/1.73 m2) Exclusion: - Post-transplant lymphoproliferative disease - Uncontrolled infection - Mental illness or other condition preventing full cooperation with the treatment and monitoring requirements of the study - ATG within the previous 14 days - Other immunosuppressive agents (including monoclonal antibodies) when initiated within the previous 7 days

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
pentostatin for injection


Locations

Country Name City State
United States MD Anderson Cancer Center Houston Texas

Sponsors (1)

Lead Sponsor Collaborator
Astex Pharmaceuticals, Inc.

Country where clinical trial is conducted

United States, 

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