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Drug

Peginterferon alfa-2a

Established medicine
ClassInterferon alpha/beta receptor agonistResearchOngoing clinical research
Also known as PEG-IFN alfa-2A, Pegasys, Peginterferon Alfa-2a (E. coli), Pegylated Interfeaon alfa-2A+6 more

PEG-IFN alfa-2A, Pegasys, Peginterferon Alfa-2a (E. coli), Pegylated Interfeaon alfa-2A, Pegylated Interferon alpha 2a, Pegylated interferon alfa-2a, Pegylated interferon alpha-2a, Pegylated-interferon alfa 2a, Pegylated-interferon-alfa-2a, PEG-Interferon alfa-2A.

2
Protein targets
1
Regulatory events
Latest activity
beta

Recent clinical, regulatory, research and industry developments relating to this drug.

Effect of Low-dose Interferon-alfa2a on Peri-operative Immune Suppression

Clinical trial2025-08-01Primary completion · ClinicalTrials.gov

Approval: Pegasys (EMA)

Regulatory2002-06-20EMA

Profile

Identifiers & mechanism

Canonical identifiers, marketed brand names and mechanism, resolved across RxNorm, ChEMBL and ATC.

Canonical name
Peginterferon alfa-2a
Aliases & brands
PEG-IFN alfa-2APegasysPeginterferon Alfa-2a (E. coli)Pegylated Interfeaon alfa-2APegylated Interferon alpha 2aPegylated interferon alfa-2aPegylated interferon alpha-2aPegylated-interferon alfa 2aPegylated-interferon-alfa-2aPEG-Interferon alfa-2A
RxNorm CUI
120608
ChEMBL ID
CHEMBL1201560
ATC codes
L03AB11L03AB61
UNII
Q46947FE7K
Primary mechanism
Interferon alpha/beta receptor agonist
Regulatory jurisdictions
ema

Pharmacology & targets

2 targets

Known molecular targets and mechanisms supported by curated pharmacology databases.

AGONISTInterferon alpha/beta receptor agonist
AGONISTInterferon alpha/beta receptor agonist

Regulatory timeline

1 event

The complete regulatory record, grouped by authority — approvals, safety advisories and label changes. Each authority shows its most recent events; expand one to read its full history.

Earliest approval
2002-06-20
Latest approval
2002-06-20
Authorities
EMA
Total events
1
emaEuropean Medicines Agency· 1 event
2002-06-20Approval
Approval: Pegasys (EMA)
Indication: Polycythaemia veraPegasys is indicated as monotherapy in adults for the treatment of polycythaemia vera. Essential thrombocythaemiaPegasys is indicated as monotherapy inShow full indication

Polycythaemia veraPegasys is indicated as monotherapy in adults for the treatment of polycythaemia vera. Essential thrombocythaemiaPegasys is indicated as monotherapy in adults for the treatment of essential thrombocythaemia..Chronic hepatitis BAdult patientsPegasys is indicated for the treatment of hepatitis B envelope antigen (HBeAg)-positive or HBeAg-negative chronic hepatitis B (CHB) in adult patients with compensated liver disease and evidence of viral replication, increased alanine aminotransferase (ALT) and histologically verified liver inflammation and/or fibrosis (see sections 4.4 and 5.1).Paediatric patients 3 years of age and olderPegasys is indicated for the treatment of HBeAg-positive CHB in non-cirrhotic children and adolescents 3 years of age and older with evidence of viral replication and persistently elevated serum ALT levels. With respect to the decision to initiate treatment in paediatric patients see sections 4.2, 4.4 and 5.1.Chronic hepatitis CAdult patientsPegasys is indicated in combination with other medicinal products, for the treatment of chronic hepatitis C (CHC) in patients with compensated liver disease (see sections 4.2, 4.4 and 5.1). For hepatitis C virus (HCV) genotype specific activity, see sections 4.2 and 5.1.Paediatric patients 5 years of age and olderPegasys in combination with ribavirin is indicated for the treatment of CHC in treatment-naïve children and adolescents 5 years of age and older who are positive for serum HCV-RNA.When deciding to initiate treatment in childhood, it is important to consider growth inhibition induced by combination therapy. The reversibility of growth inhibition is uncertain. The decision to treat should be made on a case by case basis (see section 4.4).

Evidence ↗

Contains information from the European Medicines Agency (European Medicines Agency), © EMA, reused under CC BY 4.0.

Clinical trials

176 trials

The current development programme across all trial phases — status mix, phase distribution and the late-stage studies shaping the evidence base.

Development programme
CLINICALTRIALS.GOV · LIVE REGISTRY
176
registered trials across all phases
LATEST COMPLETION 2022
106
Late-stage (III+)
138
Completed
38
Discontinued
PHASE DISTRIBUTIONn = 176
Phase 113Phase 1 / 24Phase 253Phase 2 / 35Phase 348Phase 447Phase N / A6

Late-stage studies

Phase III+ trials still open or recently active — where late-stage evidence is being generated.

Recent completions

Trials that read out recently, adding to the completed evidence base.

References & data sources
  • RxNorm (U.S. National Library of Medicine) — drug identity
  • ChEMBL (EMBL-EBI) & UniProt — pharmacology and targets
  • ClinicalTrials.gov — clinical trials
  • Regulatory event sources are credited in the Regulatory Timeline above.