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Biochempeg https://www.biochempeg.com
FDA Approves Besremi (ropeginterferon
alfa-2b-njft) for Treating Polycythemia Vera
On 12 November 2021, the US Food and Drug Administration (FDA) has approved
Besremi (ropeginterferon alfa-2b-njft), developed by Pharma Essentia, for the
treatment of polycythemia vera, a blood disorder that causes overproduction of red
blood cells. Besremi is the first FDA-approved drug for the treatment of
polycythemia vera that can be taken by patients regardless of treatment history, and it is
also the first interferon therapy specifically for polycythemia vera. Previously, Besremi has
been granted orphan drug designation by the FDA for this indication and was approved by
the European Medicines Agency (EMA) in 2019.
The approval follows an evaluation of the effectiveness and safety from a Phase 3 clinical
trial. Results showed that following 7.5 years of treatment with Besremi, 61% of
patients achieved complete hematological response and 80% of patients experienced a
hematological response. The most common treatment-related adverse reactions
(incidence >40%) were flu-like illness, arthralgia, fatigue, pruritus, nasopharyngitis and
musculoskeletal pain, and serious adverse reactions (incidence >4%) were urinary tract
infection, transient ischemic attack and depression.
Biochempeg https://www.biochempeg.com
Polycythemia vera is a rare, chronic, fatal blood cancer caused by a mutation in stem cells
in the patient's bone marrow, thus resulting in the overproduction of blood cells, white
blood cells, and platelets.. This can create health risks including blood clots, stroke, and
myocardial infarction. Most cases are caused by the JAK2 V617F mutation. If not well
controlled with treatment, the disease can progress to secondary myelofibrosis and
malignancies, including acute myeloid leukemia.
Besremi is an innovative mono-pegylated, long-acting proline interferon. Benefiting
from its unique PEGylation technology, Besremi has a long activity duration in patients
with polycythemia vera, enabling dosing every two weeks or longer until hematologic
parameters are stable and allowing flexible dosing to help meet individual patient needs.
After one year of treatment, patients in complete hematologic response and stability have
the option to undergo Besremi treatment with dosing every four weeks.
The technique of covalently attaching polyethylene glycols (PEGs) to specific molecules is
known as PEGylation and is now a well-established method in the field of targeted drug
Biochempeg https://www.biochempeg.com
delivery systems. PEGylation offers several distinct pharmacological advantages
over unmodified forms, including improved drug solubility, reduced dose frequency,
toxicity and renal clearance, extended circulating life, increased drug stability, enhanced
protection against proteolytic degradation, reduced immunogenicity and antigenicity, and
minimal loss of biological activity.
Significance of PEGylated therapeutics. Image source: reference [2]
PEG is biocompatible, lacks immunogenicity, antigenicity and toxicity, is soluble in water
and other organic solvents, is readily cleared from the body and has high mobility in
solution, making this the polymer of choice for bioconjugation. Biopharma PEG, as a
leading PEG derivatives supplier, provides high purity PEG derivatives for your
drug PEGylation.
[1] U.S. FDA Approves Besremi® (ropeginterferon alfa-2b-njft) as the Only Interferon for Adults With
Polycythemia Vera. Retrieved November 12, 2021,
from https://www.businesswire.com/news/home/20211112005909/en/
[2] Prajna Mishra, Bismita Nayak, R.K. Dey, PEGylation in anti-cancer therapy: An overview, Asian
Journal of Pharmaceutical Sciences, Volume 11, Issue 3, 2016, Pages 337-348, ISSN
1818-0876, https://doi.org/10.1016/j.ajps.2015.08.011.
Biochempeg https://www.biochempeg.com
Related Articles:
Long Acting PEGylated Interferon: Application of PEG
FDA Approved PEGylated Drugs Up To 2021
Advantages and Disadvantages of PEGylated Liposomes in Drug Delivery System
Potential Limitations of PEGylated Therapeutic Proteins
​ The Applications of PEGylation Reagents

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Fda approves besremi (ropeginterferon alfa 2b-njft) for treating polycythemia vera

  • 1. Biochempeg https://www.biochempeg.com FDA Approves Besremi (ropeginterferon alfa-2b-njft) for Treating Polycythemia Vera On 12 November 2021, the US Food and Drug Administration (FDA) has approved Besremi (ropeginterferon alfa-2b-njft), developed by Pharma Essentia, for the treatment of polycythemia vera, a blood disorder that causes overproduction of red blood cells. Besremi is the first FDA-approved drug for the treatment of polycythemia vera that can be taken by patients regardless of treatment history, and it is also the first interferon therapy specifically for polycythemia vera. Previously, Besremi has been granted orphan drug designation by the FDA for this indication and was approved by the European Medicines Agency (EMA) in 2019. The approval follows an evaluation of the effectiveness and safety from a Phase 3 clinical trial. Results showed that following 7.5 years of treatment with Besremi, 61% of patients achieved complete hematological response and 80% of patients experienced a hematological response. The most common treatment-related adverse reactions (incidence >40%) were flu-like illness, arthralgia, fatigue, pruritus, nasopharyngitis and musculoskeletal pain, and serious adverse reactions (incidence >4%) were urinary tract infection, transient ischemic attack and depression.
  • 2. Biochempeg https://www.biochempeg.com Polycythemia vera is a rare, chronic, fatal blood cancer caused by a mutation in stem cells in the patient's bone marrow, thus resulting in the overproduction of blood cells, white blood cells, and platelets.. This can create health risks including blood clots, stroke, and myocardial infarction. Most cases are caused by the JAK2 V617F mutation. If not well controlled with treatment, the disease can progress to secondary myelofibrosis and malignancies, including acute myeloid leukemia. Besremi is an innovative mono-pegylated, long-acting proline interferon. Benefiting from its unique PEGylation technology, Besremi has a long activity duration in patients with polycythemia vera, enabling dosing every two weeks or longer until hematologic parameters are stable and allowing flexible dosing to help meet individual patient needs. After one year of treatment, patients in complete hematologic response and stability have the option to undergo Besremi treatment with dosing every four weeks. The technique of covalently attaching polyethylene glycols (PEGs) to specific molecules is known as PEGylation and is now a well-established method in the field of targeted drug
  • 3. Biochempeg https://www.biochempeg.com delivery systems. PEGylation offers several distinct pharmacological advantages over unmodified forms, including improved drug solubility, reduced dose frequency, toxicity and renal clearance, extended circulating life, increased drug stability, enhanced protection against proteolytic degradation, reduced immunogenicity and antigenicity, and minimal loss of biological activity. Significance of PEGylated therapeutics. Image source: reference [2] PEG is biocompatible, lacks immunogenicity, antigenicity and toxicity, is soluble in water and other organic solvents, is readily cleared from the body and has high mobility in solution, making this the polymer of choice for bioconjugation. Biopharma PEG, as a leading PEG derivatives supplier, provides high purity PEG derivatives for your drug PEGylation. [1] U.S. FDA Approves Besremi® (ropeginterferon alfa-2b-njft) as the Only Interferon for Adults With Polycythemia Vera. Retrieved November 12, 2021, from https://www.businesswire.com/news/home/20211112005909/en/ [2] Prajna Mishra, Bismita Nayak, R.K. Dey, PEGylation in anti-cancer therapy: An overview, Asian Journal of Pharmaceutical Sciences, Volume 11, Issue 3, 2016, Pages 337-348, ISSN 1818-0876, https://doi.org/10.1016/j.ajps.2015.08.011.
  • 4. Biochempeg https://www.biochempeg.com Related Articles: Long Acting PEGylated Interferon: Application of PEG FDA Approved PEGylated Drugs Up To 2021 Advantages and Disadvantages of PEGylated Liposomes in Drug Delivery System Potential Limitations of PEGylated Therapeutic Proteins ​ The Applications of PEGylation Reagents