Interferon Beta

drug
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Also known as AvonexExtaviaHuman interferon betaInterf b 1aInterf b 1bInterfb1aInterferon beta naturalInterferon-betaRebif

Summary

Interferon Beta (CHEMBL2108510) is a phase-3 clinical-stage protein (ATC L03AB02) targeting IFNAR1; indicated across 14 conditions including neoplasm and intermediate uveitis.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Protein
  • ATC class: L03AB02
  • Targets: 1 (IFNAR1)
  • Indications: 14 conditions
  • Clinical trials: 62

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2108510
NameInterferon Beta
TypeProtein
Max phase3
ATCL03AB02

Also known as: Avonex, Extavia, Human interferon beta, Interf b 1a, Interf b 1b, Interfb1a, Interferon beta, Interferon beta natural, Interferon-beta, Rebif, INTERFERON-BETA, INTERFERON BETA

Targets

Targets

Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).

GeneTargetActionpAffinityCancer dependencyUniProt
IFNAR1interferon α/β receptor 1Agonist7.80.1%P17181
Interferon-α/β receptorAgonist

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

Aggregated over 1 target gene(s): IFNAR1.

Top Reactome pathways

16 total, by targets touching each:

PathwayTargetsGenes
Cytokine Signaling in Immune system1IFNAR1
Disease1IFNAR1
Immune System1IFNAR1
Infectious disease1IFNAR1
Interferon alpha/beta signaling1IFNAR1
Regulation of IFNA/IFNB signaling1IFNAR1
Interferon Signaling1IFNAR1
Potential therapeutics for SARS1IFNAR1
SARS-CoV Infections1IFNAR1
SARS-CoV-2 Infection1IFNAR1
SARS-CoV-2 activates/modulates innate and adaptive immune responses1IFNAR1
SARS-CoV-2-host interactions1IFNAR1
Respiratory Syncytial Virus Infection Pathway1IFNAR1
Viral Infection Pathways1IFNAR1
Evasion by RSV of host interferon responses1IFNAR1
RSV-host interactions1IFNAR1

Dominant GO biological processes

GO termTargets
cell surface receptor signaling pathway via JAK-STAT1
response to virus1
response to lipopolysaccharide1
cellular response to interferon-alpha1
cellular response to interferon-beta1
type I interferon-mediated signaling pathway1
cellular response to virus1
positive regulation of cellular respiration1
regulation of transcription by RNA polymerase II1
positive regulation of metabolic process1
cytokine-mediated signaling pathway1
regulation of receptor signaling pathway via JAK-STAT1
positive regulation of protein localization to nucleus1

Indications & clinical

Indications

14 indications (1 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
neoplasm4MONDO:0005070EFO:0000616
intermediate uveitis3MONDO:0006806EFO:1000986
multiple sclerosis3MONDO:0005301MONDO:0005301
severe acute respiratory syndrome3MONDO:0005091EFO:0000694
melanoma2MONDO:0005105EFO:0000756
cutaneous neuroendocrine carcinoma1MONDO:0019210EFO:1001471
glioblastoma1MONDO:0018177EFO:0000519
oligoastrocytoma1MONDO:0016702EFO:0000630
anaplastic astrocytoma1MONDO:0016684EFO:0002499
chronic progressive multiple sclerosis1MONDO:0005284EFO:0003840
relapsing-remitting multiple sclerosis1MONDO:0005314EFO:0003929
gliosarcoma1MONDO:0016681EFO:1001465

2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 62.

Phase distribution

PhaseTrials
Not specified15
PHASE414
PHASE214
PHASE19
PHASE38
PHASE1/PHASE21
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00037102PHASE4COMPLETEDCombination Therapy With Avonex and BiMonthly High Dose Intravenous Methotrexate in Multiple Sclerosis
NCT00037115PHASE4WITHDRAWNInduction Therapy With a Single High Dose Bolus of Intravenous Methotrexate With Leucovorin Rescue, Prior to Initiation of AVONEX® Treatment, in Patients Presenting With a First Acute Demyelinating Event.
NCT00101959PHASE4WITHDRAWNImplementation Study of Treatment Optimization Recommendations on Relapsing-Remitting Multiple Sclerosis (RR MS) Subjects
NCT00146068PHASE4COMPLETEDEARLY IFNB-1a and Simvastatin Combination Therapy in Clinically Isolated Syndrome Suggestive of Multiple Sclerosis
NCT00179478PHASE4COMPLETEDLong Term Study of Avonex Therapy Following a First Attack of Multiple Sclerosis
NCT00202995PHASE4TERMINATEDRandomized Study Designed to Look at Disease Progression Using 2 Currently FDA Approved Drugs for the Treatment of RRMS
NCT00246324PHASE4COMPLETEDSafety and Efficacy Study of Doxycycline in Combination With Interferon-B-1a to Treat Multiple Sclerosis
NCT00317941PHASE4COMPLETEDSafety Study in Relapsing-remitting Multiple Sclerosis (RRMS) Patients Receiving Betaferon or Rebif
NCT00771043PHASE4WITHDRAWNA Proof-of-Concept Study to Correlate Retinal Nerve Fiber Layer Changes in Patients With Multiple Sclerosis Treated With Natalizumab or Interferon Beta 1-a
NCT01085318PHASE4COMPLETEDRebif Advanced Magnetic Resonance Imaging (MRI) and Immunology Pilot Trial
NCT01333501PHASE4COMPLETEDFingolimod Versus Interferon Beta 1b in Cognitive Symptoms
NCT02019550PHASE4COMPLETEDRebif® Rebidose® Versus Rebiject II® Ease-of-Use
NCT02234869PHASE4WITHDRAWNTransition to Peginterferon Beta-1a (BIIB017) From Subcutaneous Interferon Therapy
NCT02254304PHASE4COMPLETEDEffectiveness of Rebif® in Clinically Isolated Syndrome and Relapsing Multiple Sclerosis Using RebiSmart™
NCT00211887PHASE3COMPLETEDCombination Therapy in Patients With Relapsing-Remitting Multiple Sclerosis (MS)CombiRx
NCT00344253PHASE3COMPLETEDRandomized, Controlled Trial to Test the Efficacy of Interferon Beta in the Treatment of Intermediate Uveitis
NCT00428584PHASE3COMPLETEDRNF and Betaseron® Tolerability Study
NCT00473213PHASE3COMPLETEDOptimizing IFN Beta - 1B Dose
NCT01181115PHASE3COMPLETEDAvonex Safety and Tolerability in Chinese Subjects With Relapsing Multiple Sclerosis (MS)
NCT01252355PHASE3TERMINATEDEfficacy and Safety of Teriflunomide in Patients With Relapsing Multiple Sclerosis and Treated With Interferon-beta
NCT02937285PHASE3COMPLETEDNational Multicenter, Controlled, Single-blind Study With Two Parallel Groups Evaluating the Safety and Efficacy of Sequential Treatment With Mitoxantrone and Interferon Versus Interferon Alone in Patients With Strong Risk of Progression in the Initial Phase of Multiple Sclerosis
NCT04324463PHASE3COMPLETEDAnti-Coronavirus Therapies to Prevent Progression of Coronavirus Disease 2019 (COVID-19) Trial
NCT06510426PHASE2RECRUITINGEarly Interferon-beta Treatment for West-Nile Virus Infection
NCT00048347PHASE2COMPLETEDInterferon-beta1a (AVONEX) Treatment of Ulcerative Colitis
NCT00151801PHASE2UNKNOWNSafety and Tolerability of Interferon-Beta-1a and Estroprogestins Association in MS Patients
NCT00217295PHASE2UNKNOWNA Safety Study of Combination Treatment With Avonex and Placebo-Controlled Dosing of Topamax in Relapsing-Remitting Multiple Sclerosis
NCT00235989PHASE2COMPLETEDExtension of Prior Study Evaluating Safety and Tolerability of Two Doses of Betaseron® to Treat Relapsing-remitting Multiple Sclerosis
NCT00436826PHASE2COMPLETEDA Phase 2 Study of Cladribine Add-on to Interferon-beta (IFN-beta) Therapy in Multiple Sclerosis (MS) Subjects With Active Disease (ONWARD)
NCT00676715PHASE2COMPLETEDA Study of the Efficacy and Safety of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis
NCT00789685PHASE1/PHASE2COMPLETEDSafety, Tolerability and Preliminary Efficacy of FP-1201 in ALI and ARDS. Phase I/II
NCT00942591PHASE2COMPLETEDAtorvastatin 40 mg in Patients With Relapsing-Remitting Multiple Sclerosis Treated With Interferon-Beta-1b
NCT01071083PHASE2COMPLETEDTreatment Interruption of Natalizumab
NCT01126177PHASE2COMPLETEDComparing Efficacy and Safety of Inhaled SNG001 to Placebo
NCT01171209PHASE2COMPLETEDREsPonse to Interferon-Alpha in InterfeRon-β Neutralizing Antibody Positive Multiple Sclerosis Patients
NCT01198132PHASE2COMPLETEDA Multicentre Study of the Efficacy and Safety of Supplementary Treatment With Cholecalciferol in Patients With Relapsing Multiple Sclerosis Treated With Subcutaneous Interferon Beta-1a 44 µg 3 Times Weekly
NCT01714089PHASE2WITHDRAWNProof of Concept Study Evaluating RNS60 in the Treatment of Relapsing Remitting Multiple Sclerosis
NCT01864148PHASE2COMPLETEDStudy to Assess the Efficacy, Safety, Tolerability, and Pharmacokinetics of BIIB033 in Participants With Relapsing Forms of Multiple Sclerosis When Used Concurrently With Avonex
NCT00031083PHASE1COMPLETEDDose Escalation Study to Determine the Safety of IFN-Beta Gene Transfer in the Treatment of Grade III & Grade IV Gliomas
NCT00299962PHASE1COMPLETEDGene Therapy for Pleural Malignancies
NCT01119677PHASE1COMPLETEDA Study of Avonex to Determine the Effects of Dose Titration on the Incidence of Flu Like Symptoms in Healthy Volunteers

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).