Damoctocog alfa pegol
Damoctocog alfa pegol, sold under the brand name Jivi is a recombinant DNA-derived, Factor VIII concentrate medication used to treat hemophilia A.[1][2]
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Trade names | Jivi |
Other names | BAY94-9027, antihemophilic factor (recombinant), PEGylated-aucl |
AHFS/Drugs.com | Monograph |
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Routes of administration | Intravenous |
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Formula | C7445H11318N1984O2184S69 |
Molar mass | 165774.28 g·mol−1 |
The most common side effects include headache, cough, nausea and fever.[1]
Damoctocog alfa pegol (antihemophilic factor- recombinant pegylated-aucl) was approved for medical use in the United States in August 2018,[3] and in the European Union in November 2018.[2]
Medical uses
In the United States damoctocog alfa pegol is indicated for use in previously treated adults and adolescents (twelve years of age and older) with hemophilia A (congenital Factor VIII deficiency) for: (1) On-demand treatment and control of bleeding episodes ; (2) Perioperative management of bleeding; (3) Routine prophylaxis to reduce the frequency of bleeding episodes.[3]
In the European Union, damoctocog alfa pegol is indicated for the treatment and prophylaxis of bleeding in previously treated people twelve years of age and older with haemophilia A (congenital factor VIII deficiency).[2]
References
- "Jivi (antihemophilic factor- recombinant pegylated-aucl kit". DailyMed. 30 August 2018. Retrieved 1 October 2020.
- "Jivi EPAR". European Medicines Agency (EMA). Retrieved 1 October 2020. Text was copied from this source which is © European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
- "Jivi". U.S. Food and Drug Administration (FDA). 29 August 2018. STN: BL 125661. Retrieved 1 October 2020. This article incorporates text from this source, which is in the public domain.
External links
- "Damoctocog alfa pegol". Drug Information Portal. U.S. National Library of Medicine.
- Clinical trial number NCT01184820 for "Trial to Evaluate the Pharmacokinetics and Safety Profile of BAY94-9027 Following Single and Multiple Dose Administration" at ClinicalTrials.gov
- Clinical trial number NCT01580293 for "A Trial Investigating Safety and Efficacy of Treatment With BAY94-9027 in Severe Hemophilia A (PROTECT-VIII)" at ClinicalTrials.gov
- Clinical trial number NCT01775618 for "Safety and Efficacy of BAY94-9027 in Previously Treated Male Children With Haemophilia A" at ClinicalTrials.gov