Last update 24 May 2025

MGTA-ATACs(Heidelberg Pharma Research GmbH)

Overview

Basic Info

Drug Type
Antibody drug conjugate (ADC)
Synonyms-
Target
CD45 x c-Kit
Action
modulators, inhibitors
Mechanism
CD45 modulators(Leukocyte common antigen modulators), c-Kit inhibitors(Stem cell growth factor receptor inhibitors)
Therapeutic Areas
NeoplasmsCongenital DisordersHemic and Lymphatic Diseases
Active Indication
Genetic Diseases, InbornHematologic Neoplasms
Inactive Indication-
Originator Organization
Heidelberg Pharma Research GmbH
Active Organization
Magenta Therapeutics, Inc.Magenta Therapeutics, Inc.Heidelberg Pharma Research GmbH
Inactive Organization-
License Organization-
Drug Highest PhasePreclinical
First Approval Date-
Regulation-

Structure/Sequence

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Related

100 Clinical Results associated with MGTA-ATACs(Heidelberg Pharma Research GmbH)
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100 Translational Medicine associated with MGTA-ATACs(Heidelberg Pharma Research GmbH)
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100 Patents (Medical) associated with MGTA-ATACs(Heidelberg Pharma Research GmbH)
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100 Deals associated with MGTA-ATACs(Heidelberg Pharma Research GmbH)
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
Genetic Diseases, InbornPreclinical
United States
Magenta Therapeutics, Inc.Magenta Therapeutics, Inc.
30 Nov 2022
Genetic Diseases, InbornPreclinical
Germany
Heidelberg Pharma Research GmbH
30 Nov 2022
Hematologic NeoplasmsPreclinical
United States
Magenta Therapeutics, Inc.Magenta Therapeutics, Inc.
30 Nov 2022
Hematologic NeoplasmsPreclinical
Germany
Heidelberg Pharma Research GmbH
30 Nov 2022
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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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