Last update 22 Nov 2025

225Ac-h8C3 mAb

Overview

Basic Info

Drug Type
Radiolabeled antibody, Therapeutic radiopharmaceuticals
Synonyms
225Ac-h8C3
Target
Melanin
Action
inhibitors
Mechanism
Melanin inhibitors
Therapeutic Areas
NeoplasmsSkin and Musculoskeletal Diseases
Active Indication-
Inactive Indication
Melanoma
Originator Organization
Radimmune Therapeutics, Inc.Radimmune Therapeutics, Inc.
University of SaskatchewanUniversity of Saskatchewan
Active Organization-
Inactive Organization
University of SaskatchewanUniversity of SaskatchewanRadimmune Therapeutics, Inc.Radimmune Therapeutics, Inc.
License Organization-
Drug Highest PhasePendingPreclinical
First Approval Date-
Regulation-

Structure/Sequence

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Related

100 Clinical Results associated with 225Ac-h8C3 mAb
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100 Translational Medicine associated with 225Ac-h8C3 mAb
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100 Patents (Medical) associated with 225Ac-h8C3 mAb
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100 Deals associated with 225Ac-h8C3 mAb
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
MelanomaPreclinical
United States
Radimmune Therapeutics, Inc.Radimmune Therapeutics, Inc.
18 Nov 2020
MelanomaPreclinical
Canada
University of SaskatchewanUniversity of Saskatchewan
18 Nov 2020
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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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