Last update 24 Jan 2026

RC-278

Overview

Basic Info

Drug Type
Antibody drug conjugate (ADC)
Synonyms
RC278
Target
CDCP1 x Top I
Action
inhibitors
Mechanism
CDCP1 inhibitors(CUB domain containing protein 1 inhibitors), TOP1 inhibitors(DNA topoisomerase I inhibitors)
Therapeutic Areas
Neoplasms
Active Indication
Locally Advanced Malignant Solid NeoplasmAdvanced Malignant Solid Neoplasm
Inactive Indication-
Originator Organization
RemeGen Co., Ltd.RemeGen Co., Ltd.
Active Organization
RemeGen Co., Ltd.RemeGen Co., Ltd.
Inactive Organization-
License Organization-
Drug Highest PhasePhase 1/2
First Approval Date-
Regulation-
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Structure/Sequence

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Related

1
Clinical Trials associated with RC-278
NCT07105215
/ RecruitingPhase 1/2
A Multicenter Phase I/II Clinical Study to Evaluate the Safety and Efficacy of RC278 for Injection in the Treatment of Locally Advanced Unresectable or Metastatic Malignant Solid Tumor
100 Clinical Results associated with RC-278
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100 Translational Medicine associated with RC-278
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100 Patents (Medical) associated with RC-278
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100 Deals associated with RC-278
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Locally Advanced Malignant Solid NeoplasmPhase 2
China
RemeGen Co., Ltd.RemeGen Co., Ltd.
11 Aug 2025
Advanced Malignant Solid NeoplasmIND Approval
China
RemeGen Co., Ltd.RemeGen Co., Ltd.
18 Jul 2025
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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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