Difference between revisions of "Moxetumomab pasudotox (Lumoxiti)"
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==History of changes in FDA indication== | ==History of changes in FDA indication== | ||
− | * | + | *2018-09-13: Initial approval for adult patients with relapsed or refractory [[Hairy cell leukemia|hairy cell leukemia (HCL)]] who received at least two prior systemic therapies, including treatment with a purine nucleoside analog (PNA). ''(Based on Study 1053)'' |
− | + | ==History of changes in EMA indication== | |
+ | *2021-02-08: Initial authorization for treatment of adult patients with relapsed or refractory [[Hairy cell leukemia|hairy cell leukaemia (HCL)]] after receiving at least two prior systemic therapies. | ||
+ | *2021-07-23: Authorization withdrawn at manufacturer request, for commercial reasons | ||
==Also known as== | ==Also known as== | ||
+ | *'''Generic name:''' moxetumomab pasudotox-tdfk | ||
*'''Code names:''' CAT-8015, HA22 | *'''Code names:''' CAT-8015, HA22 | ||
*'''Brand name:''' Lumoxiti | *'''Brand name:''' Lumoxiti | ||
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[[Category:Intravenous medications]] | [[Category:Intravenous medications]] | ||
− | |||
[[Category:Immunotoxin]] | [[Category:Immunotoxin]] | ||
− | [[Category:Anti-CD22 | + | [[Category:Anti-CD22 immunotoxins]] |
[[Category:Hairy cell leukemia medications]] | [[Category:Hairy cell leukemia medications]] | ||
[[Category:FDA approved in 2018]] | [[Category:FDA approved in 2018]] | ||
+ | [[Category:EMA approved in 2021]] | ||
+ | [[Category:EMA withdrawn in 2021]] |
Latest revision as of 22:29, 3 July 2023
Mechanism of action
A recombinant immunotoxin consisting of the Fv portion of the anti-CD22 antibody covalently fused to a 38 KDa fragment of Pseudomonas exotoxin-A (PE38)
Diseases for which it is used
History of changes in FDA indication
- 2018-09-13: Initial approval for adult patients with relapsed or refractory hairy cell leukemia (HCL) who received at least two prior systemic therapies, including treatment with a purine nucleoside analog (PNA). (Based on Study 1053)
History of changes in EMA indication
- 2021-02-08: Initial authorization for treatment of adult patients with relapsed or refractory hairy cell leukaemia (HCL) after receiving at least two prior systemic therapies.
- 2021-07-23: Authorization withdrawn at manufacturer request, for commercial reasons
Also known as
- Generic name: moxetumomab pasudotox-tdfk
- Code names: CAT-8015, HA22
- Brand name: Lumoxiti