Last update 31 Jan 2026

Anti-CDH17/CD3 bispecific antibody(Tavotek)

Overview

Basic Info

Drug Type
Bispecific T-cell Engager (BiTE)
Synonyms-
Target
CD3 x CDH17
Action
stimulants, antagonists
Mechanism
CD3 stimulants(T cell surface glycoprotein CD3 stimulants), CDH17 antagonists(Cadherin-17 antagonists)
Therapeutic Areas
NeoplasmsDigestive System DisordersRespiratory Diseases+ [1]
Active Indication-
Inactive Indication
Breast CancerColorectal CancerLung Cancer+ [1]
Originator Organization
Tuochuang Biotechnology Suzhou Co Ltd.Tuochuang Biotechnology Suzhou Co Ltd.
Active Organization-
Inactive Organization
Tuochuang Biotechnology Suzhou Co Ltd.Tuochuang Biotechnology Suzhou Co Ltd.
License Organization-
Drug Highest PhaseDiscontinuedDiscovery
First Approval Date-
Regulation-

Related

100 Clinical Results associated with Anti-CDH17/CD3 bispecific antibody(Tavotek)
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100 Translational Medicine associated with Anti-CDH17/CD3 bispecific antibody(Tavotek)
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100 Patents (Medical) associated with Anti-CDH17/CD3 bispecific antibody(Tavotek)
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100 Deals associated with Anti-CDH17/CD3 bispecific antibody(Tavotek)
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Breast CancerDiscovery
China
Tuochuang Biotechnology Suzhou Co Ltd.Tuochuang Biotechnology Suzhou Co Ltd.
01 Aug 2022
Colorectal CancerDiscovery
China
Tuochuang Biotechnology Suzhou Co Ltd.Tuochuang Biotechnology Suzhou Co Ltd.
01 Aug 2022
Lung CancerDiscovery
China
Tuochuang Biotechnology Suzhou Co Ltd.Tuochuang Biotechnology Suzhou Co Ltd.
01 Aug 2022
Stomach CancerDiscovery
China
Tuochuang Biotechnology Suzhou Co Ltd.Tuochuang Biotechnology Suzhou Co Ltd.
01 Aug 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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