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Patients with CD22(+) B-cell lymphomas will be treated with escalating doses as a 192 hr infusion of immunotoxin in a Phase I study to determine dose limiting toxicity evidence of response.
Patients with CD22(+) B-cell lymphomas will be treated with escalating doses as a 192 hr infusion of immunotoxin in a Phase I study to determine dose limiting toxicity evidence of response.
Age
All ages
Sex
ALL
Healthy Volunteers
No
National Cancer Institute (NCI)
Bethesda, Maryland, United States
Start Date
July 1, 1991
Completion Date
April 1, 2001
Last Updated
March 4, 2008
24
Estimated participants
IgG-RFB4-SMPT-dgA
DRUG
Lead Sponsor
National Cancer Institute (NCI)
NCT05006716
NCT06026319
Data Source & Attribution
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