Last update 23 May 2026

Pertuzumab biosimilar (Biocad)

Overview

Basic Info

Drug Type
Biosimilar, Monoclonal antibody
Synonyms
BCD 178, BCD-178
Target
HER2
Action
antagonists
Mechanism
HER2 antagonists(Receptor tyrosine-protein kinase erbB-2 antagonists), ADCC(Antibody-dependent cell-mediated cytotoxicity (ADCC) effects)
Therapeutic Areas
NeoplasmsSkin and Musculoskeletal Diseases
Active Indication
HER2 Positive Breast Cancer
Inactive Indication-
Originator Organization
Biocad CJSCBiocad CJSC
Active Organization
Biocad CJSCBiocad CJSC
Inactive Organization-
License Organization-
Drug Highest PhasePhase 3
First Approval Date-
Regulation-
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Structure/Sequence

Related

2
Clinical Trials associated with Pertuzumab biosimilar (Biocad)
NCT05802225
/ Active, not recruitingPhase 3
A Double-Blind, Randomized Clinical Study of the Efficacy and Safety of BCD-178 and Perjeta? as Neoadjuvant Therapy of HER2-Positive Breast Cancer
NCT05738993
/ Unknown statusPhase 1
A Double-Blind, Comparative, Randomized Clinical Study of the Pharmacokinetics, Safety, and Immunogenicity of a Single Intravenous Infusion of BCD-178 or Perjeta® in Healthy Volunteers
100 Clinical Results associated with Pertuzumab biosimilar (Biocad)
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100 Translational Medicine associated with Pertuzumab biosimilar (Biocad)
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100 Patents (Medical) associated with Pertuzumab biosimilar (Biocad)
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100 Deals associated with Pertuzumab biosimilar (Biocad)
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
HER2 Positive Breast CancerPhase 3
Russia
Biocad CJSCBiocad CJSC
30 Jan 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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