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Last update 08 Nov 2025
Nivolumab biosimilar(Biocad)
Last update 08 Nov 2025
Overview
Basic Info
Drug Type Biosimilar, Monoclonal antibody |
Synonyms BCD 263, BCD-263, BCD263 |
Target |
Action inhibitors |
Mechanism PD-1 inhibitors(Programmed cell death protein 1 inhibitors) |
Therapeutic Areas |
Active Indication |
Inactive Indication- |
Originator Organization |
Active Organization |
Inactive Organization- |
License Organization- |
Drug Highest PhasePhase 3 |
First Approval Date- |
Regulation- |
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Structure/Sequence
Sequence Code 93681
Sequence Code 93684
Related
2
Clinical Trials associated with Nivolumab biosimilar(Biocad)NCT06640530
A Double-Blind, Randomized Clinical Study of the Efficacy and Safety of BCD-263 and Opdivo? as Monotherapy in Subjects With Advanced Melanoma of the Skin
NCT06112808
A Double-Blind, Randomized Clinical Study of the Pharmacokinetics and Safety of BCD-263 and Opdivo® as Monotherapy in Subjects With Advanced Melanoma of the Skin
100 Clinical Results associated with Nivolumab biosimilar(Biocad)
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100 Translational Medicine associated with Nivolumab biosimilar(Biocad)
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100 Patents (Medical) associated with Nivolumab biosimilar(Biocad)
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100 Deals associated with Nivolumab biosimilar(Biocad)
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External Link
| KEGG | Wiki | ATC | Drug Bank |
|---|---|---|---|
| - | - | - |
R&D Status
10 top R&D records. to view more data
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| Indication | Highest Phase | Country/Location | Organization | Date |
|---|---|---|---|---|
| Locally Advanced Melanoma | Phase 3 | Belarus | 21 Mar 2024 | |
| Locally Advanced Melanoma | Phase 3 | Pakistan | 21 Mar 2024 | |
| Locally Advanced Melanoma | Phase 3 | Russia | 21 Mar 2024 | |
| Melanoma, Cutaneous Malignant | Phase 3 | Belarus | 21 Mar 2024 | |
| Melanoma, Cutaneous Malignant | Phase 3 | Pakistan | 21 Mar 2024 | |
| Melanoma, Cutaneous Malignant | Phase 3 | Russia | 21 Mar 2024 |
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Clinical Result
Clinical Result
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Translational Medicine
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Deal
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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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Regulation
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