Leukemia Clinical Trial
Official title:
Phase I Trial of Targeted Atomic Nano-Generators (Actinium-225-Labeled Humanized Anti-CD33 Monoclonal Antibody HuM195) in Patients With Advanced Myeloid Malignancies
The purpose of this study is to find a safe dose of actinium-225 when it is labeled to
HuM195. This will be done with a "phase I trial," in which a preset schedule of doses gets
more powerful for each new group of patients as the trial progresses. If too many serious
side effects are seen with a certain dose, no one will be treated with a higher dose, and
some additional patients may be treated with a lower dose to make sure that this dose is
safe. The starting dose of actinium-225 in this study is less than doses that are known to
be safe in animals.
Antibodies are proteins that are produced by the immune system and help the body to fight
foreign substances, such as bacteria or viruses. HuM195 was made by putting human leukemia
cells into mice. Most of the mouse parts of this antibody were replaced with human parts.
Only the part of the antibody that binds to the leukemia cells was kept from the mouse.
HuM195 attaches to leukemia cells but does not attach to most normal cells. It can kill
small amounts of disease by identifying the leukemia cells as "foreign." HuM195 has worked
less well against large amounts of leukemia since the normal immune cells needed to kill
leukemia cells are lowered in most patients with leukemia.
n/a
Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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