Last update 25 Oct 2025

Monoclonal antibody G250RIT(Janssen Biotech)

Overview

Basic Info

Drug Type
Radiolabeled antibody, Therapeutic radiopharmaceuticals
Synonyms
WX-G250RIT
Target
CAIX
Action
modulators
Mechanism
CAIX modulators(Carbonic anhydrase IX modulators)
Therapeutic Areas
NeoplasmsDigestive System DisordersUrogenital Diseases
Active Indication-
Inactive Indication
Biliary Tract NeoplasmsKidney NeoplasmsRenal Cell Carcinoma
Originator Organization
Janssen Biotech, Inc.Janssen Biotech, Inc.
Active Organization-
Inactive Organization
Janssen Global Services LLCJanssen Global Services LLCWilex GmbH Im- u. Export von Investitions- und Verbrauchsgüter
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 Monoclonal antibody G250RIT(Janssen Biotech)
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100 Translational Medicine associated with Monoclonal antibody G250RIT(Janssen Biotech)
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100 Patents (Medical) associated with Monoclonal antibody G250RIT(Janssen Biotech)
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100 Deals associated with Monoclonal antibody G250RIT(Janssen Biotech)
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Biliary Tract NeoplasmsPhase 2
Netherlands
Wilex GmbH Im- u. Export von Investitions- und Verbrauchsgüter
-
Biliary Tract NeoplasmsPhase 2-
Janssen Global Services LLCJanssen Global Services LLC
-
Kidney NeoplasmsPhase 2
Germany
Wilex GmbH Im- u. Export von Investitions- und Verbrauchsgüter
-
Renal Cell CarcinomaPhase 2-
Wilex GmbH Im- u. Export von Investitions- und Verbrauchsgüter
-
Renal Cell CarcinomaPhase 2-
Janssen Global Services LLCJanssen Global Services LLC
-
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

No Data

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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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