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    <copyright>© 2026 MJH Life Sciences™ and The Center For Biosimilars. All rights reserved.</copyright>
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      <title><![CDATA[Rituximab Biosimilars Show Comparable 6-Month Outcomes in AAV]]></title>
      <link>https://www.centerforbiosimilars.com/view/rituximab-biosimilars-show-comparable-6-month-outcomes-in-aav</link>
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      <pubDate>Fri, 14 Aug 2026 18:26:18 +0000</pubDate>
      <description><![CDATA[Rituximab biosimilars showed no significant 6-month differences vs the originator in antineutrophil cytoplasmic antibody–associated vasculitis (AAV).]]></description>
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      <title><![CDATA[Adalimumab Biosimilar Sustains Efficacy After Switch in Saudi Cohort]]></title>
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      <pubDate>Tue, 11 Aug 2026 13:00:00 +0000</pubDate>
      <description><![CDATA[Saudi real-world study finds adalimumab biosimilar switching preserves efficacy and safety, with full response in patients with HS.]]></description>
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      <title><![CDATA[Analytical Characterization Supports Confidence in Monoclonal Antibody Biosimilars]]></title>
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      <pubDate>Thu, 06 Aug 2026 13:00:00 +0000</pubDate>
      <description><![CDATA[Analytical characterization supports monoclonal antibody biosimilar approvals and may reduce clinical testing needs, researchers found.]]></description>
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      <title><![CDATA[Biosimilar Denosumab Shows Cost-Effectiveness Over Bisphosphonates in PMO]]></title>
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      <pubDate>Tue, 04 Aug 2026 18:51:24 +0000</pubDate>
      <description><![CDATA[Biosimilar denosumab cleared a $150,000 per QALY cost-effectiveness threshold against bisphosphonates for high-risk PMO, but not always at $100,000.]]></description>
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      <title><![CDATA[Biosimilars Round Up: July 2026]]></title>
      <link>https://www.centerforbiosimilars.com/view/biosimilars-round-up-july-2026</link>
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      <pubDate>Tue, 04 Aug 2026 15:56:16 +0000</pubDate>
      <description><![CDATA[Congress advances biosimilar bills as new data emerge on romosozumab, tirzepatide, and ustekinumab biosimilar development.]]></description>
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      <title><![CDATA[Denosumab Biosimilar KN012 Matches Reference Drug in Phase 3 Osteoporosis Trial]]></title>
      <link>https://www.centerforbiosimilars.com/view/denosumab-biosimilar-kn012-matches-reference-drug-in-phase-3-osteoporosis-trial</link>
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      <pubDate>Thu, 30 Jul 2026 21:10:13 +0000</pubDate>
      <description><![CDATA[KN012 achieved BMD equivalence with US-approved denosumab in postmenopausal women in China. ]]></description>
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      <title><![CDATA[India's Anti-VEGF Biosimilars Cut Costs, Expand Access]]></title>
      <link>https://www.centerforbiosimilars.com/view/india-s-anti-vegf-biosimilars-cut-costs-expand-access</link>
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      <pubDate>Thu, 30 Jul 2026 20:00:00 +0000</pubDate>
      <description><![CDATA[Anti-VEGF biosimilars in India matched reference therapy, lowered costs, and improved treatment access and adherence for retinal diseases.]]></description>
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      <title><![CDATA[Eculizumab Biosimilar Shows Durable Benefit in Long-Term aHUS]]></title>
      <link>https://www.centerforbiosimilars.com/view/eculizumab-biosimilar-shows-durable-benefit-in-long-term-ahus</link>
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      <pubDate>Wed, 29 Jul 2026 16:46:01 +0000</pubDate>
      <description><![CDATA[A 50-patient study found sustained platelet recovery and low thrombotic microangiopathy rates through 52 weeks of biosimilar therapy, with favorable safety.]]></description>
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      <title><![CDATA[Biosimilar Bills Gain Steam in Congress, But Key Reforms Still Wait]]></title>
      <link>https://www.centerforbiosimilars.com/view/biosimilar-bills-gain-steam-in-congress-but-key-reforms-still-wait</link>
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      <pubDate>Thu, 23 Jul 2026 19:39:07 +0000</pubDate>
      <description><![CDATA[Congress fast-tracks biosimilar bills to cut drug and insulin costs, while patent, rebate, and reimbursement roadblocks still stall competition.]]></description>
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      <title><![CDATA[Aflibercept Biosimilar SB15 Shows Real-World Efficacy Across Retinal Diseases]]></title>
      <link>https://www.centerforbiosimilars.com/view/aflibercept-biosimilar-sb15-shows-real-world-efficacy-across-retinal-diseases</link>
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      <pubDate>Wed, 22 Jul 2026 20:14:23 +0000</pubDate>
      <description><![CDATA[Aflibercept biosimilar SB15 improved retinal anatomy while preserving vision in both treatment-naïve and switching patients with nAMD, RVO, and DME.]]></description>
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      <title><![CDATA[Biosimilar Ranibizumab Performs on Par With Innovator Drug Across Retinal Diseases]]></title>
      <link>https://www.centerforbiosimilars.com/view/biosimilar-ranibizumab-performs-on-par-with-innovator-drug-across-retinal-diseases</link>
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      <pubDate>Tue, 21 Jul 2026 13:40:01 +0000</pubDate>
      <description><![CDATA[Nearly 5000 eyes and nearly 21,000 injections show comparable vision, anatomical, and safety outcomes between biosimilar ranibizumab and the innovator drug.]]></description>
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      <title><![CDATA[Real-World Natalizumab Biosimilar Switch Reduced Treatment Satisfaction Despite Stable Outcomes]]></title>
      <link>https://www.centerforbiosimilars.com/view/real-world-natalizumab-biosimilar-switch-reduced-treatment-satisfaction-despite-stable-outcomes</link>
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      <pubDate>Mon, 20 Jul 2026 17:30:00 +0000</pubDate>
      <description><![CDATA[Real-world natalizumab biosimilar switching preserved relapsing-remitting MS outcomes but lowered treatment satisfaction, likely due to a nocebo effect.
]]></description>
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      <title><![CDATA[Romosozumab Biosimilar Matches Reference in Functional Testing Despite Disulfide Differences]]></title>
      <link>https://www.centerforbiosimilars.com/view/romosozumab-biosimilar-matches-reference-in-functional-testing-despite-disulfide-differences</link>
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      <pubDate>Thu, 16 Jul 2026 18:00:00 +0000</pubDate>
      <description><![CDATA[A romosozumab biosimilar showed comparable sclerostin binding and bone-signaling potency to the reference product despite disulfide isoform differences.
]]></description>
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      <title><![CDATA[FDA Accepts Sandoz Generic Tirzepatide Applications Amid Biosimilar Development Gap]]></title>
      <link>https://www.centerforbiosimilars.com/view/fda-accepts-sandoz-generic-tirzepatide-applications-amid-biosimilar-development-gap</link>
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      <pubDate>Mon, 13 Jul 2026 15:21:44 +0000</pubDate>
      <description><![CDATA[Sandoz moves toward US generic tirzepatide autoinjectors as FDA reviews ANDAs, signaling future GLP‑1 access amid patent and biosimilar gaps.]]></description>
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      <title><![CDATA[Anti-VEGF Biosimilars Match Reference Drug in Indian Retinal Disease Care]]></title>
      <link>https://www.centerforbiosimilars.com/view/anti-vegf-biosimilars-match-reference-drug-in-indian-retinal-disease-care</link>
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      <pubDate>Thu, 09 Jul 2026 14:44:42 +0000</pubDate>
      <description><![CDATA[Biosimilar anti-VEGF agents matched the reference ranibizumab in vision outcomes and safety across retinal diseases in India, at a lower cost.]]></description>
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      <title><![CDATA[Rituximab Biosimilar Reached 75% Remission, Matched Innovator in Membranous Nephropathy]]></title>
      <link>https://www.centerforbiosimilars.com/view/rituximab-biosimilar-reached-75-remission-matched-innovator-in-membranous-nephropathy</link>
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      <pubDate>Wed, 08 Jul 2026 15:36:21 +0000</pubDate>
      <description><![CDATA[Real-world data shows rituximab biosimilars for membranous nephropathy match remission rates, cut costs, and expand treatment options.]]></description>
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      <title><![CDATA[Biosimilar ABP 654 Maintains Efficacy, Safety After Repeated Switching From Ustekinumab]]></title>
      <link>https://www.centerforbiosimilars.com/view/biosimilar-abp-654-maintains-efficacy-safety-after-repeated-switching-from-ustekinumab</link>
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      <pubDate>Tue, 07 Jul 2026 11:00:00 +0000</pubDate>
      <description><![CDATA[Trial data show switching between ABP 654 and reference ustekinumab maintains similar psoriasis control, safety, and immunogenicity, supporting FDA interchangeability confidence.]]></description>
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      <title><![CDATA[Biosimilar Denosumab Matches Reference Drug for Bone Density in Chinese Women]]></title>
      <link>https://www.centerforbiosimilars.com/view/biosimilar-denosumab-matches-reference-drug-for-bone-density-in-chinese-women</link>
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      <pubDate>Mon, 06 Jul 2026 15:27:22 +0000</pubDate>
      <description><![CDATA[Phase 3 data show denosumab biosimilar KN012 matches Prolia for BMD gains and safety, potentially expanding affordable osteoporosis care.]]></description>
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      <title><![CDATA[Biosimilar Makers Push Forward on Regulatory and Commercial Fronts]]></title>
      <link>https://www.centerforbiosimilars.com/view/biosimilar-makers-push-forward-on-regulatory-and-commercial-fronts</link>
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      <pubDate>Thu, 02 Jul 2026 19:07:00 +0000</pubDate>
      <description><![CDATA[FDA expands Tofidence uses, Teva launches Eylea biosimilar in Europe, and Alvotech’s Entyvio rival enters FDA review—boosting access.]]></description>
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      <title><![CDATA[Positioning Biosimilar Ustekinumab Early Reduces Burden on Spain's National Health System]]></title>
      <link>https://www.centerforbiosimilars.com/view/positioning-biosimilar-ustekinumab-early-reduces-burden-on-spain-s-national-health-system</link>
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      <pubDate>Fri, 26 Jun 2026 14:48:23 +0000</pubDate>
      <description><![CDATA[Early use of ustekinumab biosimilars in Spain shows cost-effective Crohn disease care, boosting QALYs and cutting NHS spend—insights for Europe.]]></description>
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      <title><![CDATA[Global Biosimilar Rules Diverge Across WHO Regions, Limiting Patient Access]]></title>
      <link>https://www.centerforbiosimilars.com/view/global-biosimilar-rules-diverge-across-who-regions-limiting-patient-access</link>
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      <pubDate>Wed, 24 Jun 2026 13:42:34 +0000</pubDate>
      <description><![CDATA[Global review reveals uneven biosimilar rules on waivers, interchangeability, and safety tracking—barriers to cheaper biologics and approvals.]]></description>
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      <title><![CDATA[Low Biosimilar Awareness in MS Patients Points to Critical Gap in Nurse-Led Education]]></title>
      <link>https://www.centerforbiosimilars.com/view/low-biosimilar-awareness-in-ms-patients-points-to-critical-gap-in-nurse-led-education</link>
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      <pubDate>Thu, 18 Jun 2026 16:30:00 +0000</pubDate>
      <description><![CDATA[Italian study finds most MS patients start biosimilars unaware, exposing education gaps and highlighting MS nurses as key to boosting trust and uptake.]]></description>
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      <title><![CDATA[Biosimilar Expansion, Lower Costs Drive Shift in RA Treatment Guidelines]]></title>
      <link>https://www.centerforbiosimilars.com/view/biosimilar-expansion-lower-costs-drive-shift-in-ra-treatment-guidelines</link>
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      <pubDate>Thu, 18 Jun 2026 13:00:00 +0000</pubDate>
      <description><![CDATA[New EULAR guidelines speed RA treatment switches as rheumatoid arthritis biosimilars and cost savings push earlier biologics use.]]></description>
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      <title><![CDATA[FDA Approves Ranibizumab-hkdz as First Interchangeable, Available in Both Vials and Prefilled Syringes]]></title>
      <link>https://www.centerforbiosimilars.com/view/fda-approves-ranibizumab-hkdz-as-first-interchangeable-available-in-both-vials-and-prefilled-syringes</link>
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      <pubDate>Wed, 17 Jun 2026 20:15:51 +0000</pubDate>
      <description><![CDATA[The FDA has approved ranibizumab-hkdz (Ranluspec; Lupin Limited) as an interchangeable biosimilar for wet AMD, DME, DR, RVO, and mCNV.]]></description>
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      <title><![CDATA[Biosimilar Switching Maintained Disease Control in People With Ankylosing Spondylitis]]></title>
      <link>https://www.centerforbiosimilars.com/view/biosimilar-switching-maintained-disease-control-in-people-with-ankylosing-spondylitis</link>
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      <pubDate>Tue, 16 Jun 2026 19:37:07 +0000</pubDate>
      <description><![CDATA[Evidence shows biosimilars switching in ankylosing spondylitis maintains disease control with biologics, cuts costs, and highlights nocebo risks.]]></description>
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      <title><![CDATA[FDA Approves First Biosimilars Interchangeable With Simponi/Simponi Aria]]></title>
      <link>https://www.centerforbiosimilars.com/view/fda-approves-first-biosimilars-interchangeable-with-simponi-simponi-aria</link>
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      <pubDate>Wed, 10 Jun 2026 13:00:00 +0000</pubDate>
      <description><![CDATA[Immgolis and Immgolis Intri have the same indications as Simponi and Simponi Aria, treating patients with rheumatoid arthritis and ulcerative colitis. The biosimilars will be available in the fourth quarter of this year.]]></description>
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      <title><![CDATA[Biosimilar Adoption and Provider Performance in Medicare Value-Based Payment Models]]></title>
      <link>https://www.centerforbiosimilars.com/view/biosimilar-adoption-and-provider-performance-in-medicare-value-based-payment-models</link>
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      <pubDate>Tue, 09 Jun 2026 15:42:27 +0000</pubDate>
      <description><![CDATA[Evidence suggests that adoption of oncology biosimilars in Medicare value-based payment models has produced substantial cost savings and improved provider financial performance.]]></description>
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      <title><![CDATA[FDA Approves Immgolis and Immgolis Intri as First Biosimilars to Golimumab Reference Products for RA and UC]]></title>
      <link>https://www.centerforbiosimilars.com/view/fda-approves-immgolis-and-immgolis-intri-as-first-biosimilars-to-golimumab-reference-products-for-ra-and-uc</link>
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      <category>us</category>
      <pubDate>Mon, 08 Jun 2026 19:06:59 +0000</pubDate>
      <description><![CDATA[FDA approval clears interchangeable golimumab biosimilars for rheumatoid arthritis and ulcerative colitis, promising lower-cost TNF therapy.]]></description>
      <media:credit role="publishing company">The Center For Biosimilars</media:credit>
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    <item>
      <title><![CDATA[No Efficacy Loss After Multiple Ustekinumab Biosimilar Switches in Psoriasis]]></title>
      <link>https://www.centerforbiosimilars.com/view/no-efficacy-loss-after-multiple-ustekinumab-biosimilar-switches-in-psoriasis</link>
      <source url="https://www.centerforbiosimilars.com/rss">The Center For Biosimilars Articles</source>
      <category>us</category>
      <pubDate>Thu, 02 Apr 2026 16:36:01 +0000</pubDate>
      <description><![CDATA[Real-world study shows plaque psoriasis stays controlled after 2 ustekinumab biosimilar switches, with stable labs and no serious adverse events.]]></description>
      <media:credit role="publishing company">The Center For Biosimilars</media:credit>
      <guid>https://www.centerforbiosimilars.com/view/no-efficacy-loss-after-multiple-ustekinumab-biosimilar-switches-in-psoriasis</guid>
    </item>
    <item>
      <title><![CDATA[FDA Approves Teva Biosimilar for Denosumab in Osteoporosis]]></title>
      <link>https://www.centerforbiosimilars.com/view/fda-approves-teva-biosimilar-for-denosumab-in-osteoporosis</link>
      <source url="https://www.centerforbiosimilars.com/rss">The Center For Biosimilars Articles</source>
      <category>us</category>
      <pubDate>Tue, 31 Mar 2026 14:03:08 +0000</pubDate>
      <description><![CDATA[The FDA approved Teva’s biosimilar for denosumab, and the FDA and EMA accepted its asthma biosimilar application for review.]]></description>
      <media:credit role="publishing company">The Center For Biosimilars</media:credit>
      <guid>https://www.centerforbiosimilars.com/view/fda-approves-teva-biosimilar-for-denosumab-in-osteoporosis</guid>
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