Last update 31 May 2025

Epratuzumab I-131

Overview

Basic Info

Drug Type
Radiolabeled antibody, Therapeutic radiopharmaceuticals
Synonyms
Anti-CD22 monoclonal antibody LL2-I-131, Monoclonal antibody LL2-I-131, IMMU LL2-I-131
+ [2]
Target
CD22
Action
modulators
Mechanism
CD22 modulators(CD22 modulators), ADCC(Antibody-dependent cell-mediated cytotoxicity (ADCC) effects)
Therapeutic Areas
NeoplasmsImmune System DiseasesHemic and Lymphatic Diseases
Active Indication-
Inactive Indication
Non-Hodgkin Lymphoma
Originator Organization
Immunomedics, Inc.Immunomedics, Inc.
Active Organization-
Inactive Organization
Repligen Corp.Repligen Corp.Immunomedics, Inc.Immunomedics, Inc.
License Organization-
Drug Highest PhaseDiscontinuedPhase 2
First Approval Date-
Regulation-
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Structure/Sequence

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Related

100 Clinical Results associated with Epratuzumab I-131
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100 Translational Medicine associated with Epratuzumab I-131
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100 Patents (Medical) associated with Epratuzumab I-131
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100 Deals associated with Epratuzumab I-131
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Non-Hodgkin LymphomaPhase 2
United States
--
Non-Hodgkin LymphomaPhase 2-
Repligen Corp.Repligen Corp.
-
Non-Hodgkin LymphomaPhase 2-
Immunomedics, Inc.Immunomedics, Inc.
-
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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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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Biosimilar

Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.
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Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.

Regulation

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