Last update 08 May 2025

Tri-modal CAR+TCR+hnCD16+iPSC-derived T cells(Fate)

Overview

Basic Info

Drug Type
Induced pluripotent stem cells (iPSC), CAR-T
Synonyms-
Target
BCMA x CD16a x MICA x MICB x NY-ESO-1
Action
inhibitors, modulators
Mechanism
BCMA inhibitors(B-cell maturation protein inhibitors), CD16a modulators(Low affinity immunoglobulin gamma Fc region receptor III-A modulators), MICA inhibitors(MHC class I polypeptide-related sequence A inhibitors)
+ [2]
Therapeutic Areas
Neoplasms
Active Indication
Solid tumor
Inactive Indication-
Originator Organization
Fate Therapeutics, Inc.Fate Therapeutics, Inc.
Active Organization
Fate Therapeutics, Inc.Fate Therapeutics, Inc.
Inactive Organization-
License Organization-
Drug Highest PhasePreclinical
First Approval Date-
Regulation-

Related

100 Clinical Results associated with Tri-modal CAR+TCR+hnCD16+iPSC-derived T cells(Fate)
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100 Translational Medicine associated with Tri-modal CAR+TCR+hnCD16+iPSC-derived T cells(Fate)
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100 Patents (Medical) associated with Tri-modal CAR+TCR+hnCD16+iPSC-derived T cells(Fate)
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100 Deals associated with Tri-modal CAR+TCR+hnCD16+iPSC-derived T cells(Fate)
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
Solid tumorPreclinical
United States
Fate Therapeutics, Inc.Fate Therapeutics, Inc.
10 Nov 2022
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
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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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