Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 3:31 PM
Ignite Modification Date:
2025-12-24 @ 3:31 PM
NCT ID:
NCT00710892
Eligibility Criteria:
INCLUSION CRITERIA:
At the time of transplant:
A. Patients (up to 65 years of age) with:
1. ALL or high grade NHL that is Stage III or IV and has relapsed or is considered to be primary refractory disease.
2. Myelodysplastic syndrome.
3. AML after first relapse or with primary refractory disease.
4. CML
5. Hemophagocytic lymphohistiocytosis (HLH); familial hemophagocytic lymphohistiocytosis (FLH); viral-associated hemophagocytic syndrome (VAHS); patients with severe chronic active Epstein Barr virus infection (SCAEBV) with predilection for T or NK cell malignancy; X-linked lymphoproliferative disease (XLP)
B. Lack of suitable conventional donor (i.e. 5/6 or 6/6 related, or 5/6 or 6/6 unrelated donor) or presence of a rapidly progressive disease not permitting time to identify an unrelated donor.
At the time of allodepleted T cell infusion:
1. Engrafted with ANC greater than 500.
2. Must have greater than or equal to 50% donor chimerism in either peripheral blood or bone marrow, or relapse of their original disease.
3. Life expectancy greater than 30 days
4. Lansky/Karnofsky scores greater than or equal to 60
5. Absence of severe renal disease (creatinine greater than 2X normal for age)
6. Absence of severe hepatic disease (direct bilirubin greater than 2 mg/dL, or SGOT greater than 200
7. Oxygen saturation greater than 94% on room air
8. Patient/Guardian able to give informed consent
EXCLUSION CRITERIA:
At the time of transplant:
1\. Pregnancy\*
At the time of allodepleted T cell infusion:
1. GvHD
2. Severe intercurrent infection
3. Pregnancy\*
4. Other investigational drugs in the prior 30 days
* Pregnancy test only required for at-risk individuals, defined as female patients of childbearing potential who have received a reduced-intensity conditioning regimen.
Healthy Volunteers:
False
Sex:
ALL
Maximum Age:
65 Years
Study:
NCT00710892
Study Brief:
Protocol Section:
NCT00710892