Overview
Human interferon beta (166 residues), glycosylated, MW=22.5kD. It is produced by mammalian cells (Chinese Hamster Ovary cells) into which the human interferon beta gene has been introduced. The amino acid sequence is identical to that of natural human interferon beta.
Indication
For treatment of relapsing/remitting multiple sclerosis, also for condyloma acuminatum
Associated Conditions
- Relapsing Multiple Sclerosis (RMS)
Research Report
Interferon Beta-1a (DB00060): A Comprehensive Monograph on its Biotechnological Production, Pharmacology, Clinical Efficacy, and Safety Profile in the Management of Multiple Sclerosis
I. Executive Summary
Interferon beta-1a is a recombinant human glycoprotein that represents a foundational, first-generation disease-modifying therapy (DMT) for multiple sclerosis (MS). As a biotech drug produced in mammalian cells, its structure, including critical glycosylation, is identical to that of endogenous human interferon beta. This monograph provides a comprehensive analysis of its molecular characteristics, manufacturing processes, pharmacological profile, clinical development, and extensive safety record.
The primary mechanism of action for interferon beta-1a is immunomodulatory. By binding to Type I interferon receptors, it initiates a complex intracellular signaling cascade via the Jak/STAT pathway, leading to the transcriptional regulation of over 100 genes. The cumulative effect is a shift away from pro-inflammatory and toward anti-inflammatory processes, a reduction in the migration of inflammatory cells across the blood-brain barrier, and a dampening of the autoimmune response directed against the central nervous system. While the precise mechanisms remain incompletely elucidated, this activity translates into a clinically meaningful reduction in relapse rates and a slowing of disability accumulation in patients with relapsing forms of MS.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2025/05/31 | Phase 2 | Not yet recruiting | |||
2024/07/19 | Phase 2 | Recruiting | |||
2023/09/26 | N/A | Active, not recruiting | |||
2023/08/31 | Phase 2 | Recruiting | German Society for Pediatric Oncology and Hematology GPOH gGmbH | ||
2022/12/20 | N/A | Recruiting | |||
2022/03/28 | Phase 2 | Recruiting | |||
2021/08/27 | Not Applicable | Completed | |||
2021/02/01 | Phase 3 | Completed | |||
2020/12/01 | Phase 3 | UNKNOWN | |||
2020/08/19 | Phase 2 | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Biogen Inc. | 59627-002 | INTRAMUSCULAR | 30 ug in 0.5 mL | 11/22/2022 | |
EMD Serono, Inc. | 44087-3344 | SUBCUTANEOUS | 44 ug in 0.5 mL | 7/31/2023 | |
EMD Serono, Inc. | 44087-0022 | SUBCUTANEOUS | 22 ug in 0.5 mL | 7/31/2023 | |
EMD Serono, Inc. | 44087-0044 | SUBCUTANEOUS | 44 ug in 0.5 mL | 7/31/2023 | |
EMD Serono, Inc. | 44087-3322 | SUBCUTANEOUS | 22 ug in 0.5 mL | 7/31/2023 | |
Biogen Inc. | 59627-003 | INTRAMUSCULAR | 30 ug in 0.5 mL | 11/22/2022 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
Authorised | 3/13/1997 | ||
Authorised | 5/3/1998 |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
Rebif Solution for Injection in Cartridge 22mcg/0.5ml | SIN13974P | INJECTION, SOLUTION | 22mcg/0.5ml | 6/17/2011 | |
Rebif Solution for Injection in Cartridge 44mcg/0.5ml | SIN13975P | INJECTION, SOLUTION | 44mcg/0.5ml | 6/17/2011 |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
---|---|---|---|---|---|
No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
---|---|---|---|---|---|
AVONEX SOLUTION FOR INJECTION IN PRE-FILLED PEN 30MCG/0.5ML | N/A | N/A | N/A | 10/22/2013 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
REBIF 44 interferon beta-1a (rch) 132 microgram/1.5mL solution for injection multidose cartridge | 165746 | Medicine | A | 1/21/2010 | |
REBIF 22 interferon beta-1a (rch) 22 microgram/0.5mL injection pre-filled syringe | 133809 | Medicine | A | 12/5/2008 | |
AVONEX interferon beta-1a (rch) 30microgram/0.5mL injection pre-filled syringe | 95419 | Medicine | A | 5/4/2004 | |
REBIF 22 interferon beta-1a (rch) 66 microgram/1.5mL solution for injection multidose cartridge | 165745 | Medicine | A | 1/21/2010 | |
REBIF 44 interferon beta-1a (rch) 44 microgram/0.5mL injection pre-filled syringe autoinjector | 174479 | Medicine | A | 10/21/2010 | |
REBIF 44 interferon beta-1a (rch) 44 microgram/0.5mL injection pre-filled syringe | 133813 | Medicine | A | 12/5/2008 | |
AVONEX PEN | 180136 | Medicine | A | 11/22/2011 | |
REBIF 22 interferon beta-1a (rch) 22 microgram/0.5mL injection pre-filled syringe autoinjector | 174478 | Medicine | A | 10/21/2010 |
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