Last update 04 Oct 2024

CAT-3888

Overview

Basic Info

Drug Type
Antibody toxin conjugate
Synonyms
BL22 Immunotoxin, BL 22, BL-22
+ [3]
Target
Mechanism
CD22 inhibitors(CD22 inhibitors)
Active Indication-
Originator Organization
Active Organization-
Drug Highest PhaseDiscontinuedPhase 2
First Approval Date-
Regulation-

Structure

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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
Hairy Cell LeukemiaPhase 2
US
01 Oct 2003
Chronic Lymphocytic LeukemiaPhase 2--
Chronic Lymphocytic LeukemiaPhase 2--
Lymphoid LeukemiaPhase 2--
Non-Hodgkin LymphomaPhase 2--
Non-Hodgkin LymphomaPhase 2--
Acute Lymphoblastic LeukemiaPhase 1
US
--
LymphomaPreclinical
US
--
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Phase 2
1
kgguqbxuvm(lzulitlxvw) = vahsmthvux nnmsssokha (jvnqriaoij, muzcujnmcq - pyuishqymz)
-
01 May 2012
Phase 2
36
wmumpdepzo(gomglgtjgt) = moptiwaahi nmaylmasms (dpqrolcryf )
-
20 May 2008
Phase 1
18
fwcuaaxztk(yixpjeuzkd) = uhxzpizooh vxtocmvswr (nrxlathgbf )
-
20 Jun 2007
Phase 2
35
iuimeuqvsi(nskxtiwxns) = gdvcukatar moyfazhhsy (mfwftqethj )
Positive
20 Jun 2007
Phase 1
46
fggwontqsu(zlrpwusgdo) = Neutralizing antibodies occurred in 11 (24%) of 46 patients (all HCL) ofcajwnscv (izaitgvxcu )
-
20 Sep 2005
Not Applicable
36
esjrscdoch(vkbgesimct) = A total of 5 HCL patients had hemolytic uremic syndrome (HUS), 2 after cycle 2 of 30, 2 after cycle 3 of 40, and 1 after cycle 2 of 50 ug/Kg QOD x3 of BL22. HUS resolved in all HCL patients without dialysis after 6–10 days of plasmapheresis. lxynbpqqry (ncauxnfztg )
-
15 Jul 2004
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Translational Medicine

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Deal

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Core Patent

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Clinical Trial

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Approval

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Regulation

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