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Interferon beta-1b

Interferon beta-1b is a recombinant form of the naturally occurring human cytokine interferon beta, produced using genetically engineered bacteria, and is primarily indicated for the treatment of relapsing forms of (MS), including , relapsing-remitting MS, and active secondary progressive MS, to reduce the frequency of clinical exacerbations and delay disability progression. Approved by the U.S. (FDA) in 1993 under the brand name Betaseron, it was the first disease-modifying therapy for MS and is marketed as Extavia since 2009, both administered as a subcutaneous injection every other day at a dose of 0.25 mg. The precise mechanism of action of interferon beta-1b in remains incompletely understood, but it is believed to exert immunomodulatory effects by binding to specific surface receptors, thereby inducing the expression of genes that promote pathways, suppress proinflammatory production, reduce T-cell activation and migration across the blood-brain barrier, and inhibit matrix metalloproteinases involved in demyelination. Clinical trials, such as the pivotal 1993 III , demonstrated that it reduces the annualized relapse rate by approximately 30% and decreases MRI activity, supporting its role in altering the disease course. Common side effects include flu-like symptoms (fever, chills, fatigue), injection-site reactions (pain, redness, swelling), and lymphopenia, while more serious risks encompass , , , pulmonary arterial hypertension, and increased infection susceptibility, necessitating regular monitoring of liver function, blood counts, and . As a biologic , beta-1b has been a of management for over three decades, though its use has evolved with the advent of oral and higher-efficacy alternatives, and it is contraindicated in patients with to human albumin or beta.

Pharmacology

Mechanism of action

Interferon beta-1b is a recombinant form of human beta, a belonging to the type I interferon family, produced in with a serine substitution at position 17 to enhance stability. It exerts its effects by binding to the heterodimeric (IFNAR) complex, composed of IFNAR1 and IFNAR2 subunits, on the surface of various cell types including immune cells and endothelial cells. This binding initiates a conformational change in the receptor, recruiting and activating Janus kinase 1 (JAK1) and tyrosine kinase 2 (TYK2). Upon receptor activation, the is engaged, where phosphorylated and STAT2 form a complex with interferon regulatory factor 9 (IRF9) to create interferon-stimulated gene factor 3 (ISGF3), which translocates to the and induces transcription of hundreds of s (ISGs). These ISGs encode proteins with antiviral, antiproliferative, and immunomodulatory functions, such as MxA (an antiviral ) and PKR (a that inhibits ). The pathway's activation leads to pleiotropic biological activities that modulate immune responses without directly targeting viral pathogens in the context of therapy. Key immunomodulatory effects of interferon beta-1b include enhancement of suppressor T-cell (Treg) activity, which promotes by inhibiting autoreactive T cells, and reduction of pro-inflammatory production, such as interferon-gamma (IFN-γ) and tumor necrosis factor-alpha (TNF-α), while promoting anti-inflammatory cytokines like interleukin-10 (IL-10). It also downregulates (MHC) class II expression on antigen-presenting cells, thereby decreasing to T cells and limiting pro-inflammatory activation. Additionally, interferon beta-1b upregulates MHC class I proteins on target cells, facilitating cytotoxic T-cell recognition and clearance of infected or abnormal cells while avoiding excessive inflammation. In the , interferon beta-1b inhibits blood-brain barrier () disruption by reducing the activity of matrix metalloproteinases (MMPs), particularly MMP-9, which degrade components and facilitate immune cell entry. This reduction restores the balance with tissue inhibitors of metalloproteinases (TIMPs), stabilizing the BBB integrity. Furthermore, it decreases the migration of activated T cells into the CNS by downregulating adhesion molecules on endothelial cells, such as vascular cell adhesion molecule-1 (VCAM-1), thereby limiting inflammatory infiltration.

Pharmacokinetics

Interferon beta-1b is administered by subcutaneous injection as the standard route. Following subcutaneous administration, the drug exhibits incomplete absorption, resulting in a bioavailability of approximately 50% based on studies with doses up to 0.5 mg. Peak serum concentrations are achieved within 1 to 8 hours post-injection, with mean peak levels around 40 IU/mL at higher doses in healthy volunteers; however, at the recommended therapeutic dose of 0.25 mg, serum concentrations are often low or undetectable due to rapid clearance and a short elimination half-life. The pharmacokinetics demonstrate a biphasic elimination profile, with an initial alpha phase half-life of approximately 0.25 to 0.5 hours and a terminal beta phase half-life of 2 to 3 hours, though values up to 5 hours have been reported in some intravenous and subcutaneous studies. The drug is primarily distributed to the , reflected in a steady-state ranging from 0.25 L/kg to 2.88 L/kg following intravenous administration. Interferon beta-1b does not significantly cross the blood-brain barrier but produces its therapeutic effects through systemic . Metabolism occurs via proteolytic degradation and , with clearance mediated mainly through hepatic and renal routes at rates of 9.4 to 28.9 mL/min/kg; there is no significant involvement of enzymes in its metabolism. Pharmacokinetics are not strictly dose-proportional at therapeutic levels, as serum levels remain low despite dose increases, and steady-state concentrations are not applicable given the every-other-day dosing schedule and lack of drug accumulation. shows interpatient variability influenced by factors such as injection site and body mass, leading to irregular profiles. In patients with hepatic impairment, use with caution and liver due to the risk of , though specific pharmacokinetic data in this population are limited. No major drug interactions have been identified that significantly alter the of interferon beta-1b.

Clinical applications

Indications

Interferon beta-1b is primarily indicated for the treatment of relapsing forms of () to reduce the frequency of clinical exacerbations and delay the progression of physical disability. This includes patients with relapsing-remitting (RRMS), where it serves as a disease-modifying therapy aimed at mitigating inflammatory activity and lesion development in the . It is also approved for the treatment of (), defined as a first demyelinating event suggestive of , particularly in patients with MRI features consistent with the disease, to delay the conversion to clinically definite . The () similarly authorizes its use in patients with a single severe demyelinating event requiring intravenous corticosteroids and at high risk of developing , after exclusion of alternative diagnoses. An extended indication covers secondary progressive MS (SPMS) with active disease, characterized by ongoing relapses, where interferon beta-1b has demonstrated efficacy in reducing rates and slowing progression. However, it is not indicated for primary progressive MS (PPMS), as clinical evidence does not support its use in this non-relapsing form. Likewise, interferon beta-1b lacks approval for non-MS conditions, and off-label applications, such as in certain viral infections, are not endorsed by the FDA or due to insufficient robust evidence. Patient selection typically focuses on individuals with early-stage relapsing , including or RRMS, who have no contraindications such as to the drug or decompensated , positioning it as a first-line disease-modifying in appropriate cases. Guidelines from organizations like the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) recommend its initiation in patients with active relapsing disease to optimize long-term outcomes.

Efficacy

Interferon beta-1b demonstrated efficacy in reducing rates in patients with relapsing-remitting (RRMS) in the pivotal randomized, double-blind, -controlled trial conducted by the IFNB . In this study involving 372 ambulatory patients with RRMS, the annual rate was 1.31 in the group compared to 0.90 in the group receiving 8 million international units (MIU) of interferon beta-1b every other day over 2 years, representing approximately 31% reduction (p=0.0001). Additionally, the treatment delayed the time to sustained progression in disability as measured by the (EDSS), with more patients in the high-dose group remaining exacerbation-free at 2 years (36 versus 18 in ; p=0.007). In (CIS) suggestive of , early initiation of interferon beta-1b reduced the risk of conversion to clinically definite (CDMS). The trial extension showed a 45% risk reduction in conversion to CDMS over 3 years compared to delayed treatment ( 0.55; 95% CI 0.41-0.74; p=0.0001). For established RRMS, meta-analyses of clinical trials confirm that interferon beta-1b achieves a 20-30% reduction in annualized rate (ARR), alongside decreased MRI lesion activity and slowed disability progression based on EDSS scores. In secondary progressive multiple sclerosis (SPMS), the European Betaferon trial demonstrated a modest delay in confirmed progression with interferon beta-1b. Among 718 patients, treatment delayed progression by 9-12 months over 2-3 years ( 0.65; 95% CI 0.52-0.83; p=0.0008), though no significant ARR reduction was observed in the subgroup with non-active SPMS. Long-term follow-up data from the original , extending up to 16 years, indicate sustained reduction in relapse frequency with early interferon beta-1b use but limited impact on ultimate accumulation. Comparative efficacy analyses show that interferon beta-1b has similar effects to other beta-interferons in reducing ARR by approximately 30% in RRMS but is inferior to newer oral disease-modifying therapies, such as or , which achieve greater ARR reductions (up to 50%). No head-to-head trials establish superiority among beta-interferons.

Administration and dosing

Interferon beta-1b is administered via subcutaneous injection every other day at a standard dose of 0.25 mg (250 mcg or 8 million international units), with the initial injection typically performed under healthcare provider supervision to ensure proper technique. To minimize flu-like symptoms, initiation involves a schedule over six weeks, starting at 0.0625 mg every other day and increasing incrementally as follows:
WeeksDose (mg)Volume (mL)% of Recommended Dose
1–20.06250.2525%
3–40.1250.5050%
5–60.18750.7575%
7+0.251.00100%
This regimen allows gradual adaptation while reaching the full therapeutic dose. Patients are trained for self-administration, rotating injection sites among the , buttocks, thighs, and upper arms to prevent skin reactions; aseptic technique is required, and needles or syringes should not be reused. The lyophilized powder is reconstituted with 1.2 mL of provided diluent (0.54% solution) by gentle swirling—avoiding shaking—and used immediately or stored refrigerated at 2–8°C for up to 3 hours; it remains stable for 3 hours at room temperature post-reconstitution if needed. Unreconstituted vials should be stored at 2–30°C, with excursions permitted, and protected from light; do not freeze. During initiation and ongoing therapy, regular monitoring includes blood tests for liver function, (including differential and platelets), and function at 1, 3, and 6 months, then periodically, to detect potential abnormalities early. No dose adjustments are typically required for renal impairment, though caution is advised in hepatic disease with close monitoring of due to risk of injury. Use during is not recommended, as indicate potential fetal harm at exposures ≥3 times the human dose, despite human observational data showing no increased risk of major birth defects; previous FDA classification was C.

Adverse effects

Common side effects

Interferon beta-1b therapy is commonly associated with flu-like symptoms, affecting approximately 57% of patients in controlled clinical trials, including fever, chills, fatigue, , , and , which typically occur within hours of injection and have a median duration of 7.5 days. These symptoms often diminish in incidence over time, decreasing to about 10% after prolonged treatment, and can be managed effectively with using analgesics or antipyretics such as acetaminophen or ibuprofen on injection days. Injection site reactions are reported in up to 78% of patients, manifesting as (42%), pain (16%), (4%), redness, swelling, or bruising, with rare instances of (4%). These local reactions are generally mild and decrease in frequency with continued use; proper injection technique and rotation of sites (, , hips, thighs) help minimize severity and prevent complications. Laboratory abnormalities frequently include (18% vs. 6% placebo), lymphopenia, and elevated liver enzymes such as (up to 12% with levels >5x baseline) and (4%), which are typically reversible upon dose reduction or discontinuation. Regular monitoring of complete blood counts and is recommended to detect these changes early. Other common adverse effects encompass asthenia (53%), headache (50%), myalgia (23%), rash (21%), menstrual disorders, hair thinning, and mild depression, often derived from post-marketing surveillance data. Dose titration, starting at lower doses and gradually increasing, can reduce the overall incidence of these effects while maintaining efficacy in multiple sclerosis patients.

Serious adverse effects

Interferon beta-1b can cause hepatic injury, manifesting as severe elevations in liver enzymes or acute , with elevations of SGPT greater than five times the upper limit of normal occurring in approximately 12% of patients compared to 4% on , and severe cases including reported in post-marketing surveillance. Such events, though infrequent (less than 1% for symptomatic severe injury), necessitate immediate discontinuation of the if , , or other signs of hepatic dysfunction appear, alongside regular monitoring of . Hematologic adverse effects include and severe , with reported in 13% of patients versus 5% on , and in 18% versus 6%. These occur in less than 5% as severe events requiring intervention, prompting recommendations for monthly monitoring, particularly in the initial treatment phase, to detect myelosuppression early. has been noted primarily in post-marketing reports. Neuropsychiatric reactions encompass severe , suicidal ideation, and , with or suicide attempts observed in clinical trials at rates leading to three suicides and eight attempts among treated patients compared to one suicide and four attempts on , equating to an approximate 1-5% incidence for severe mood disorders. Pre-treatment screening for mood disorders is advised, and patients should be monitored closely, with discontinuation considered if severe symptoms emerge; has been reported post-marketing. Hypersensitivity reactions such as or are rare, occurring sporadically in post-marketing data, while neutralizing development affects 30-45% of patients, potentially reducing efficacy but not typically linked to severe . Immediate discontinuation is required for anaphylactic events, with monitoring for allergic symptoms like dyspnea recommended. Other serious risks include seizures, particularly in patients with a history of epilepsy, temporally associated with treatment but without established causality; increased susceptibility to infections due to immunomodulatory effects; and a potential association with malignancy, though no causal link has been confirmed in studies. Patients with seizure history should report events promptly, and general infection vigilance is advised during administration. Post-marketing surveillance has identified very rare events such as and pulmonary arterial , with frequency unknown and no definitive causal relationship established, requiring symptom reporting for ophthalmologic or cardiopulmonary changes.

Contraindications and precautions

beta-1b is contraindicated in patients with a history of to natural or recombinant beta, human , or . It is also contraindicated in individuals with decompensated . Relative precautions are advised for patients with a history of severe or attempts, as the drug may exacerbate psychiatric symptoms; close monitoring is essential, and discontinuation should be considered if severe develops. Caution is recommended in those with active infections due to the potential for increasing infection risk, severe cardiac conditions such as congestive where worsening may occur, and during owing to teratogenic risks observed in animal studies—effective contraception is advised for women of childbearing potential. Drug interactions may include additive myelosuppression when combined with other immunosuppressants, such as corticosteroids, necessitating careful monitoring of blood counts. Increased is possible with concomitant use of hepatotoxic drugs, so should be assessed prior to initiation. Monitoring requirements encompass baseline and periodic evaluations of , complete blood counts, thyroid function, and neurologic status to detect potential complications early. Discontinuation is warranted for persistent severe laboratory abnormalities, such as significant elevations or , or for uncontrolled side effects like worsening or hepatic injury. Interferon beta-1b is not approved for use in children under 18 years, as and have not been established in this . In elderly patients, data are limited, and use requires caution due to higher risks, including cardiac and hepatic issues.

History and development

Discovery and early research

Interferons were first discovered in by Alick Isaacs and Jean Lindenmann, who identified them as soluble proteins produced by virus-infected cells that confer resistance to viral infection in neighboring cells, marking a foundational advance in understanding innate antiviral immunity. This discovery stemmed from studies on viral interference in chick embryo membranes, revealing interferons as non-antibody mediators of cellular protection against viruses. In the , research differentiated types of interferons, with beta-interferon (IFN-β) specifically identified as the form produced by human fibroblasts in response to viral stimuli, distinguishing it from the leukocyte-derived alpha-interferon. By the , preclinical investigations demonstrated that type I interferons, including IFN-β, could suppress exacerbations in animal models of (MS), such as experimental autoimmune (EAE), by modulating immune responses in myelin-reactive T cells. For instance, early studies showed that administration of type I interferons reduced disease severity in EAE through anti-inflammatory effects on . The recombinant production of human IFN-β advanced in 1980 when David V. Goeddel and colleagues at cloned the human IFN-β gene and expressed it in , enabling large-scale bacterial synthesis of the protein. This prokaryotic expression system yielded IFN-β-1b, a non-glycosylated variant differing from the naturally glycosylated form produced in eukaryotic cells. The development of IFN-β-1b specifically involved collaboration between Berlex Laboratories and , which focused on optimizing the recombinant protein for therapeutic potential. Preclinical studies of IFN-β-1b established its immunomodulatory properties, including reduced T-cell proliferation and enhanced suppressor T-cell activity , as well as antiviral efficacy against encephalomyocarditis virus . Toxicity profiles were characterized in and non-human primates, revealing dose-dependent flu-like symptoms and mild hepatic effects but overall tolerability at therapeutic levels. The rationale for exploring IFN-β-1b in arose from the hypothesis that the disease involves immune-mediated demyelination driven by a Th1-dominant response, with type I interferons promoting a shift toward Th2 cytokines to restore immune balance. This , supported by EAE observations, laid the groundwork for subsequent therapeutic evaluation.

Pivotal clinical trials

The pivotal clinical trials for interferon beta-1b (IFNB-1b) primarily focused on its efficacy and safety in relapsing-remitting (RRMS), secondary progressive (SPMS), and (CIS). The landmark IFNB Multiple Sclerosis Study Group trial, conducted from 1988 to 1993, enrolled 372 ambulatory patients with RRMS in a multicenter, randomized, double-blind, -controlled . Patients were assigned to receive , 1.6 million international units (MIU) of IFNB-1b, or 8 MIU (equivalent to 250 mcg) subcutaneously every other day for up to 5 years, with a mean follow-up of 2 years. The primary endpoint was the annual rate, assessed alongside secondary measures including (EDSS) progression and (MRI) evaluations of lesion activity and burden. In the 250 mcg dose group, IFNB-1b reduced the exacerbation rate by 29% compared to (1.31 vs. 1.85 exacerbations per year; p=0.023), with fewer moderate-to-severe exacerbations and a significant decrease in new or enlarging MRI lesions (p<0.001). Long-term follow-up of this cohort extended to 16 years in an open-label, involving 88% of original participants, confirming sustained safety with no new serious risks but showing no significant difference in EDSS progression between early treatment and groups, indicating plateaued long-term impact on disability. For SPMS, the 1998 multicenter trial randomized 718 patients to 250 mcg IFNB-1b or subcutaneously every other day for up to 3 years in a double-blind, -controlled design. The primary endpoint was time to sustained EDSS progression by at least 1 point (or 0.5 points if EDSS ≥6.0), confirmed after 6 months. IFNB-1b delayed progression ( 0.70; 95% CI 0.54-0.90; p=0.0058), with greater benefits in subgroups with active disease (recent s), including a 22% reduction in relapse rate and fewer active MRI lesions (p<0.0001), though no effect was observed in inactive SPMS. The BENEFIT trial (2006-2007 core phase) evaluated early treatment in , randomizing 468 patients with a first demyelinating event and at least two silent T2 lesions to immediate 250 mcg IFNB-1b every other day or (delayed treatment after conversion to clinically definite [CDMS] or 24 months), in a double-blind design with 3-year follow-up. Primary endpoints included time to CDMS (Poser criteria) and McDonald diagnosis, with secondary assessments of disability via EDSS and MRI outcomes. Early IFNB-1b reduced the risk of CDMS by 45% ( 0.55; 95% 0.38-0.80; p=0.0017) and McDonald by 36% ( 0.64; 95% 0.47-0.86; p=0.003), alongside fewer new MRI lesions. An open-label extension to 5 years (2009) and beyond (up to 11 years in 2016) sustained these benefits, with early treatment linked to lower EDSS progression and reduced . No major phase III trials for IFNB-1b have emerged since , though from registries like MSBase has validated trial findings on reduction and stabilization in diverse, long-term cohorts. These pivotal studies faced limitations, including high dropout rates (up to 48% over 5 years in extensions, often due to injection-site reactions and flu-like symptoms) that may bias efficacy estimates toward completers. Additionally, trial populations lacked ethnic and racial diversity, predominantly enrolling White patients from and , potentially limiting generalizability to global MS demographics.

Regulatory approvals

Interferon beta-1b received its initial regulatory approval from the U.S. (FDA) on July 23, 1993, under the brand name Betaseron, developed by (later Berlex Laboratories), for the treatment of relapsing-remitting (RRMS) in ambulatory patients to reduce the frequency of clinical exacerbations; it was the first disease-modifying therapy approved for . In Europe, the European Medicines Agency (EMA) granted marketing authorization for Betaferon on November 30, 1995, for the treatment of RRMS. This approval was expanded in January 2006 to include secondary progressive multiple sclerosis (SPMS) with active disease, based on evidence from clinical trials demonstrating reduced disability progression. Further expansion occurred in 2007 to cover clinically isolated syndrome (CIS) suggestive of multiple sclerosis, allowing early intervention to delay conversion to clinically definite MS. Approvals followed in other regions, including by in December 1994 for RRMS, by the in 1995 for RRMS, and by the Ministry of Health, Labour and Welfare in January 2007 for relapsing forms of MS. A pediatric investigation plan for interferon beta-1b was accepted by the in 2013, but as of 2025, it remains unapproved for pediatric use due to insufficient data on safety and efficacy in children under 18 years. Label expansions in the United States included updates in 1995 incorporating (MRI) data from pivotal trials, supporting its role in reducing the frequency and severity of MRI-detected lesions. Post-2000 label revisions by the FDA emphasized monitoring for neutralizing antibodies, which can develop in up to 30-50% of patients and may reduce clinical efficacy, recommending periodic testing to guide treatment decisions. In 2009, the FDA approved Extavia, a formulation of interferon beta-1b by Pharmaceuticals Corporation, on August 14, via an abbreviated pathway as a follow-on product to Betaseron, with identical indications for relapsing forms of including a first clinical . The marketing authorisation for Extavia was withdrawn in the on November 25, 2024, at the request of the marketing authorisation holder for commercial reasons. As of , no major new indications have been approved for interferon beta-1b globally, though product s continue to carry warnings for severe hepatic injury (including rare cases of hepatic failure) and (with monitoring advised due to risks of ), updates to which were incorporated in the based on post-marketing . It remains recommended in clinical guidelines, such as the American Academy of Neurology's 2018 practice guideline on disease-modifying therapies for adults with , as an option for reducing relapses in relapsing forms.

Formulations and availability

Commercial products

Interferon beta-1b is commercially available primarily under two branded products in the United States: Betaseron, manufactured by HealthCare Pharmaceuticals, and Extavia, manufactured by Pharmaceuticals. Betaseron is supplied as a lyophilized containing 0.3 mg of interferon beta-1b per single-dose , which is reconstituted with 1.2 mL of 0.54% to yield a 0.25 mg/mL solution for subcutaneous injection of 1 mL (0.25 mg dose) every other day. The formulation includes human and as stabilizers. It is packaged in kits consisting of 15 vials, along with corresponding diluent syringes, vial adapters, and needles, and is compatible with the BETACONNECT auto-injector device for easier self-administration. Unreconstituted Betaseron has a of up to 3 years when stored at (20°C to 25°C), with excursions permitted to 15°C to 30°C for up to 3 months; reconstituted solution must be used within 3 hours if refrigerated at 2°C to 8°C. Extavia offers a nearly identical to Betaseron and is approved by the FDA as a follow-on biologic demonstrating therapeutic equivalence. It is provided as 0.3 mg of lyophilized interferon beta-1b powder per single-dose , reconstituted similarly with 1.2 mL of 0.54% to produce a 0.25 mg/mL solution for the standard 0.25 mg dose. Packaging includes cartons of 15 blister units, each containing a , pre-filled , adapter with 27-gauge needle, and alcohol prep pads. packs are available to support the recommended initiation schedule, starting at 0.0625 mg and escalating over 6 weeks to minimize side effects. Like Betaseron, unreconstituted Extavia is stable for 3 years at 20°C to 25°C, with excursions to 15°C to 30°C allowed for up to 3 months, and reconstituted solution is usable within 3 hours under . Both products are supplied in single-use vials or kits to ensure sterility and ease of , with no major discontinued formulations reported as of 2025. The annual list price for either Betaseron or Extavia exceeds $70,000 USD as of 2025, though actual costs vary by insurance coverage. assistance programs, such as Bayer's BETAPLUS copay support and US Patient Assistance Foundation, as well as Novartis's offerings, provide financial including $0 copay options and free medication for eligible uninsured or underinsured patients.

Biosimilars and generics

Extavia, approved by the U.S. (FDA) in 2009, represents the first follow-on biologic to the original interferon beta-1b product Betaseron, demonstrating similarity in and through pharmacokinetic and pharmacodynamic studies. Other biosimilars have emerged primarily in select markets, such as Ziferon in for treatment and Ronbetal in , reflecting limited global approvals due to the inherent of biologic processes. No true small-molecule generics are possible for interferon beta-1b, as it is a complex recombinant protein requiring biological production methods. Regulatory pathways for include the FDA's 351(k) abbreviated licensure pathway, established under the 2010 Biologics Price Competition and Innovation Act, which mandates comparative analytical, nonclinical, and clinical studies to confirm similarity to the reference product. The () has followed a similar framework since 2006, emphasizing totality of evidence for biosimilar approval, including assessments. In competitive markets like and , biosimilars have reduced treatment costs by up to 30% compared to originators, enhancing access in low- and middle-income countries, though overall uptake remains constrained by the subcutaneous injection regimen and persistent high out-of-pocket expenses. Key challenges include potential differences in , with biosimilars requiring rigorous post-approval monitoring for neutralizing antibody formation that could impact efficacy. As of 2025, no new major biosimilars have received FDA or approval, with research and development efforts increasingly shifting toward next-generation disease-modifying therapies for . Research continues for biosimilars in emerging markets, such as South-East , though none meet FDA or standards as of 2025.