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Norris Cotton Cancer CenterNorris Cotton Cancer Center
In This Section
 
A Phase I/II Study of De-immunized DI-Leu16-IL2 Immunocytokine Administered Subcutaneously in Patients with B-cell Non-Hodgkin Lymphoma (NHL)
Principal Investigator (?)
Lansigan, Frederick
Study Number
F13023
Summary
An open-label, dose-escalation trial of the safety, tolerability, pharmacokinetics (PK), biological, and clinical activity of DI-Leu16-IL2 administered to patients with CD20 (B-lymphocyte antigen CD20) positive Non-Hodgkin Lymphoma (NHL) that have failed standard rituximab-containing therapy. Following peripheral blood B cell depletion with rituximab (if needed) each patient will receive DI-Leu16-IL2 administered as a subcutaneous (SC) injection for three consecutive days every three weeks. 
Phase (?)
Phase III
Sponsor (?)
Contact

Darcie Findley

Available at the following location(s)

Lebanon

View more details from ClinicalTrials.gov.

Contact Information

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