Last update 12 Dec 2025

TAA16/13

Overview

Basic Info

Drug Type
Bispecific antibody
Synonyms
TAA16/13_BsAb, TAA16/13
Target-
Action-
Mechanism-
Therapeutic Areas
NeoplasmsImmune System DiseasesHemic and Lymphatic Diseases+ [1]
Active Indication-
Inactive Indication
Anaplastic Large-Cell LymphomaNK-cell lymphomaPeripheral T-Cell Lymphoma
Originator Organization
PersonGen BioTherapeutics (Suzhou) Co., Ltd.PersonGen BioTherapeutics (Suzhou) Co., Ltd.
Active Organization-
Inactive Organization
PersonGen BioTherapeutics (Suzhou) Co., Ltd.PersonGen BioTherapeutics (Suzhou) Co., Ltd.
License Organization-
Drug Highest PhaseDiscontinuedPreclinical
First Approval Date-
Regulation-

Related

100 Clinical Results associated with TAA16/13
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100 Translational Medicine associated with TAA16/13
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100 Patents (Medical) associated with TAA16/13
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100 Deals associated with TAA16/13
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Anaplastic Large-Cell LymphomaPreclinical
China
PersonGen BioTherapeutics (Suzhou) Co., Ltd.PersonGen BioTherapeutics (Suzhou) Co., Ltd.
22 May 2023
NK-cell lymphomaPreclinical
China
PersonGen BioTherapeutics (Suzhou) Co., Ltd.PersonGen BioTherapeutics (Suzhou) Co., Ltd.
22 May 2023
Peripheral T-Cell LymphomaPreclinical
China
PersonGen BioTherapeutics (Suzhou) Co., Ltd.PersonGen BioTherapeutics (Suzhou) Co., Ltd.
22 May 2023
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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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