Last update 08 May 2025

Human Fibrinogen(Guiyang Qianfeng Biological Product Liability)

Overview

Basic Info

Drug Type
Non-recombinant coagulation factor
Synonyms-
Target
Fibrinogen
Action
stimulants
Mechanism
Fibrinogen stimulants
Therapeutic Areas
Congenital DisordersHemic and Lymphatic DiseasesOther Diseases
Active Indication-
Inactive Indication
Acquired fibrinogen deficiencyAfibrinogenemia
Originator Organization
Guiyang Qianfeng Biological Product Liability Co. Ltd.
Active Organization-
Inactive Organization
Guiyang Qianfeng Biological Product Liability Co. Ltd.
License Organization-
Drug Highest PhasePendingPhase 3
First Approval Date-
Regulation-
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Related

2
Clinical Trials associated with Human Fibrinogen(Guiyang Qianfeng Biological Product Liability)
CTR20140641
/ CompletedPhase 3
人纤维蛋白原治疗白血病引起的获得性纤维蛋白原缺乏症的 疗效及安全性的多中心临床研究
[Translation] A multicenter clinical study on the efficacy and safety of human fibrinogen in the treatment of acquired fibrinogen deficiency caused by leukemia
CTR20140119
/ CompletedPhase 3
人纤维蛋白原（FCH）治疗原发性纤维蛋白原减少或缺乏症的疗效及安全性的多中心临床研究
[Translation] A multicenter clinical study on the efficacy and safety of human fibrinogen (FCH) in the treatment of primary fibrinogen deficiency or deficiency
100 Clinical Results associated with Human Fibrinogen(Guiyang Qianfeng Biological Product Liability)
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100 Translational Medicine associated with Human Fibrinogen(Guiyang Qianfeng Biological Product Liability)
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100 Patents (Medical) associated with Human Fibrinogen(Guiyang Qianfeng Biological Product Liability)
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100 Deals associated with Human Fibrinogen(Guiyang Qianfeng Biological Product Liability)
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
Acquired fibrinogen deficiencyPhase 3
China
Guiyang Qianfeng Biological Product Liability Co. Ltd.
17 Oct 2014
AfibrinogenemiaPhase 3
China
Guiyang Qianfeng Biological Product Liability Co. Ltd.
14 Jan 2014
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
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Deal

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Clinical Trial

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Approval

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Biosimilar

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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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