Peginterferon beta-1a
Peginterferon beta-1a, sold under the brand name Plegridy, is medication used to treat multiple sclerosis.[3][4]
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Trade names | Plegridy, Plegridy Pen |
Other names | BIIB-017 |
AHFS/Drugs.com | Monograph |
MedlinePlus | a614059 |
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Routes of administration | Subcutaneous injection |
Drug class | Antineoplastic agent |
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Chemical and physical data | |
Formula | C913H1417N246O256PS7 [C2H4O]n |
Molar mass | 44 000 g·mol−1 |
The most common side effects include headache, muscle pain, joint pain, influenza (flu)-like symptoms, pyrexia (fever), chills, asthenia (weakness), and erythema (reddening of the skin), pain or pruritus (itching) at the injection site.[3][4]
Peginterferon beta-1a was approved for medical use in the United States and in the European Union in 2014.[5][4]
Medical uses
In the United States peginterferon beta-1a is indicated for the treatment of relapsing forms of multiple sclerosis, to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults.[3]
In the European Union peginterferon beta-1a is indicated for the treatment of relapsing remitting multiple sclerosis in adults.[4]
References
- "Peginterferon beta-1a (Plegridy) Use During Pregnancy". Drugs.com. 22 July 2019. Retrieved 25 June 2020.
- "Prescription medicines: registration of new chemical entities in Australia, 2014". Therapeutic Goods Administration (TGA). 21 June 2022. Retrieved 10 April 2023.
- "Plegridy- peginterferon beta-1a kit Plegridy Pen- peginterferon beta-1a kit Plegridy- peginterferon beta-1a injection, solution". DailyMed. 30 March 2020. Retrieved 25 June 2020.
- "Plegridy EPAR". European Medicines Agency (EMA). Retrieved 24 June 2020. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
- "Drug Approval Package: Plegridy (peginterferon beta-1a) prefilled syringe and Plegridy Pen (peginterferon beta-1a) prefilled pen NDA #125499". U.S. Food and Drug Administration (FDA). 17 September 2014. Retrieved 25 June 2020.