Last update 30 Oct 2025

MW-C1

Overview

Basic Info

Drug Type
Antibody drug conjugate (ADC)
Synonyms
MW C1
Target
CLDN1 x Tubulin
Action
inhibitors
Mechanism
CLDN1 inhibitors(Claudin 1 inhibitors), Tubulin inhibitors
Therapeutic Areas
NeoplasmsDigestive System DisordersRespiratory Diseases+ [1]
Active Indication
Hepatocellular CarcinomaSquamous Cell Carcinoma of Head and Necksquamous cell lung carcinoma+ [1]
Inactive Indication-
Originator Organization
Mabwell (Shanghai) Bioscience Co., Ltd.Mabwell (Shanghai) Bioscience Co., Ltd.
Active Organization
Mabwell (Shanghai) Bioscience Co., Ltd.Mabwell (Shanghai) Bioscience Co., Ltd.
Inactive Organization-
License Organization-
Drug Highest PhasePreclinical
First Approval Date-
Regulation-

Structure/Sequence

Molecular FormulaC39H67N5O7
InChIKeyDASWEROEPLKSEI-UIJRFTGLSA-N
CAS Registry474645-27-7
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Related

100 Clinical Results associated with MW-C1
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100 Translational Medicine associated with MW-C1
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100 Patents (Medical) associated with MW-C1
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100 Deals associated with MW-C1
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Hepatocellular CarcinomaPreclinical
China
Mabwell (Shanghai) Bioscience Co., Ltd.Mabwell (Shanghai) Bioscience Co., Ltd.
28 Apr 2025
Squamous Cell Carcinoma of Head and NeckPreclinical
China
Mabwell (Shanghai) Bioscience Co., Ltd.Mabwell (Shanghai) Bioscience Co., Ltd.
28 Apr 2025
squamous cell lung carcinomaPreclinical
China
Mabwell (Shanghai) Bioscience Co., Ltd.Mabwell (Shanghai) Bioscience Co., Ltd.
28 Apr 2025
Uterine Cervical CancerPreclinical
China
Mabwell (Shanghai) Bioscience Co., Ltd.Mabwell (Shanghai) Bioscience Co., Ltd.
28 Apr 2025
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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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