Last update 02 Apr 2025

Filgrastim biosimilar(CuraTeQ)

Overview

Basic Info

Drug Type
Biosimilar, Colony-stimulating factors
Synonyms
Filgrastim Biosimilar (Curateq Biologics Pvt Ltd.), 非格司亭 生物类似药（Curateq Biologics Pvt Ltd.）, BP 13
+ [3]
Target
CSF-3R
Action
agonists
Mechanism
CSF-3R agonists(Colony stimulating factor 3 receptor agonists)
Therapeutic Areas
Hemic and Lymphatic Diseases
Active Indication
Neutropenia
Inactive Indication-
Originator Organization
Curateq Biologics Pvt Ltd.
Active Organization
Curateq Biologics Pvt Ltd.
Inactive Organization-
Drug Highest PhaseApproved
First Approval Date
European Union (12 Feb 2025),
Neutropenia
Regulation-
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Structure/Sequence

Related

2
Clinical Trials associated with Filgrastim biosimilar(CuraTeQ)
CTRI/2024/09/073942
/ Not yet recruitingPhase 1
A randomized, phase 1, double-blind, single-period, two-treatment, parallel, Multiple dose, balanced, comparative pharmacokinetic, pharmacodynamic, safety and immunogenicity assessment of BP13 (Filgrastim) 300 mcg/0.5 ml PFS with US Licensed - NEUPOGEN® (filgrastim) 300 mcg/0.5 mL in a single-dose prefilled syringe in healthy adult male Subjects - NIL
ACTRN12620001341910
/ CompletedPhase 1
A Double-Blind, Randomized, Parallel, Controlled, Study to Compare Pharmacokinetics and Pharmacodynamics of BP13 (filgrastim) with EU-approved Neupogen® in Healthy Male Adult Subjects
100 Clinical Results associated with Filgrastim biosimilar(CuraTeQ)
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100 Translational Medicine associated with Filgrastim biosimilar(CuraTeQ)
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100 Patents (Medical) associated with Filgrastim biosimilar(CuraTeQ)
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100 Deals associated with Filgrastim biosimilar(CuraTeQ)
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External Link

KEGGWikiATCDrug Bank
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L03AA02
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R&D Status

10 top approved records.
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IndicationCountry/LocationOrganizationDate
Neutropenia
European Union
Curateq Biologics Pvt Ltd.
12 Feb 2025
Neutropenia
Iceland
Curateq Biologics Pvt Ltd.
12 Feb 2025
Neutropenia
Liechtenstein
Curateq Biologics Pvt Ltd.
12 Feb 2025
Neutropenia
Norway
Curateq Biologics Pvt Ltd.
12 Feb 2025
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
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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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