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        <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>
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        <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>
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        <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>
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        <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>
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        <title><![CDATA[Bone Health in Oncology: Closing Gaps, Reducing Costs, and Unlocking Biosimilar Value]]></title>
        <link>https://www.centerforbiosimilars.com/view/bone-health-in-oncology-closing-gaps-reducing-costs-and-unlocking-biosimilar-value</link>
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        <pubDate>Mon, 30 Mar 2026 17:26:51 +0000</pubDate>
        <description><![CDATA[]]></description>
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        <title><![CDATA[Biosimilar CT-P43 Matches Ustekinumab in Treating Moderate to Severe Plaque Psoriasis]]></title>
        <link>https://www.centerforbiosimilars.com/view/biosimilar-ct-p43-matches-ustekinumab-in-treating-moderate-to-severe-plaque-psoriasis</link>
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        <pubDate>Fri, 20 Mar 2026 23:15:44 +0000</pubDate>
        <description><![CDATA[A phase 3 clinical trial found that the ustekinumab biosimilar CT-P43 demonstrated equivalent efficacy, safety, and immunogenicity to reference ustekinumab in patients with moderate to severe plaque psoriasis.]]></description>
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        <title><![CDATA[Golimumab Biosimilar Matches Reference Drug in Year-Long RA Trial]]></title>
        <link>https://www.centerforbiosimilars.com/view/golimumab-biosimilar-matches-reference-drug-in-year-long-ra-trial</link>
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        <pubDate>Thu, 19 Mar 2026 15:15:59 +0000</pubDate>
        <description><![CDATA[One-year trial shows AVT05 golimumab biosimilar matches Simponi in rheumatoid arthritis, including switching, with comparable safety and immunogenicity outcomes.]]></description>
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        <title><![CDATA[Switching to Biosimilar Etanercept Shows No Impact on Efficacy, Safety Across 18 Trials]]></title>
        <link>https://www.centerforbiosimilars.com/view/switching-to-biosimilar-etanercept-shows-no-impact-on-efficacy-safety-across-18-trials</link>
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        <pubDate>Mon, 16 Mar 2026 17:00:29 +0000</pubDate>
        <description><![CDATA[Real-world evidence shows switching between etanercept products and etanercept biosimilars preserves efficacy and safety, easing concerns and highlighting nocebo challenges.]]></description>
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        <title><![CDATA[Gaps in Knowledge Persist Around Biosimilar Insulin Switching, Review Finds]]></title>
        <link>https://www.centerforbiosimilars.com/view/gaps-in-knowledge-persist-around-biosimilar-insulin-switching-review-finds</link>
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        <pubDate>Thu, 12 Mar 2026 17:45:29 +0000</pubDate>
        <description><![CDATA[Scoping review shows clinicians and patients still worry about biosimilar insulin switching, devices and safety—evidence gaps shape insulin product swaps.]]></description>
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        <title><![CDATA[Global Biosimilar Market Sees Structural Shifts, Regulatory Hurdles, and Pipeline Gains]]></title>
        <link>https://www.centerforbiosimilars.com/view/global-biosimilar-market-sees-structural-shifts-regulatory-hurdles-and-pipeline-gains</link>
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        <pubDate>Tue, 10 Mar 2026 19:37:56 +0000</pubDate>
        <description><![CDATA[Global biosimilar market shifts: Celltrion leads biosimilars in Asia, biosimilars in Europe expand, while Sandoz restructures and FDA hurdles loom.]]></description>
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        <title><![CDATA[FDA Issues Draft Guidance Aimed at Cutting Expenses for Biosimilar PK Studies]]></title>
        <link>https://www.centerforbiosimilars.com/view/fda-issues-draft-guidance-aimed-at-cutting-expenses-for-biosimilar-pk-studies</link>
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        <pubDate>Mon, 09 Mar 2026 20:30:05 +0000</pubDate>
        <description><![CDATA[Biologics eat 51% of drug spending despite being 5% of prescriptions, but the FDA's new draft guidance hopes more competition can close that gap.]]></description>
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        <title><![CDATA[Clinician Confidence in Ophthalmology Biosimilars Remains Low Across Europe]]></title>
        <link>https://www.centerforbiosimilars.com/view/clinician-confidence-in-ophthalmology-biosimilars-remains-low-across-europe</link>
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        <pubDate>Fri, 06 Mar 2026 19:38:40 +0000</pubDate>
        <description><![CDATA[A new analysis dives into why Europe’s eye clinics lag on biosimilars and how education, guidance, and smarter tenders could unlock €747 million in savings.]]></description>
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        <title><![CDATA[Biosimilars Development Roundup: Expanding Global Options Amidst Rising US Legal Hurdles]]></title>
        <link>https://www.centerforbiosimilars.com/view/biosimilars-development-roundup-expanding-global-treatment-options-amidst-rising-us-legal-hurdles</link>
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        <pubDate>Thu, 05 Mar 2026 20:37:12 +0000</pubDate>
        <description><![CDATA[CHMP backs a fifth teriparatide biosimilar as biosimilars in Europe grow, while US patent fights threaten new biologic competition.]]></description>
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        <title><![CDATA[Biosimilar-Backed Triplet Regimen Shows Feasibility in Heavily Pretreated Liver Cancer]]></title>
        <link>https://www.centerforbiosimilars.com/view/biosimilar-backed-triplet-regimen-shows-feasibility-in-heavily-pretreated-liver-cancer</link>
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        <pubDate>Fri, 27 Feb 2026 14:00:00 +0000</pubDate>
        <description><![CDATA[A phase 2 trial showed that combining targeted radiotherapy with PD-1 blockade and a bevacizumab biosimilar can elicit responses in advanced liver cancer.]]></description>
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        <title><![CDATA[Omalizumab Biosimilar Entry Linked to Expanded Patient Access, Reduced Spending]]></title>
        <link>https://www.centerforbiosimilars.com/view/omalizumab-biosimilar-entry-linked-to-expanded-patient-access-reduced-spending</link>
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        <pubDate>Thu, 26 Feb 2026 14:27:00 +0000</pubDate>
        <description><![CDATA[Budget impact analysis finds omalizumab biosimilars in Europe could cut payer costs by €641M in 5 years, expanding access and driving major omalizumab savings.]]></description>
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        <title><![CDATA[Postmenopausal Osteoporosis: Clinical Burden, Treatment Barriers, and the Evolving Role of Denosumab Biosimilars]]></title>
        <link>https://www.centerforbiosimilars.com/view/postmenopausal-osteoporosis-clinical-burden-treatment-barriers-and-the-evolving-role-of-denosumab-biosimilars</link>
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        <pubDate>Wed, 25 Feb 2026 15:44:02 +0000</pubDate>
        <description><![CDATA[]]></description>
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        <title><![CDATA[Cardinal Health Biosimilar Report: $56 Billion in Savings and the Road to Market Sustainability]]></title>
        <link>https://www.centerforbiosimilars.com/view/cardinal-health-biosimilar-report-56-billion-in-savings-and-the-road-to-market-sustainability</link>
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        <pubDate>Tue, 24 Feb 2026 14:00:00 +0000</pubDate>
        <description><![CDATA[Biosimilars save billions, but FDA’s new guidance, physician concerns, and Humira switchbacks reveal hurdles to a sustainable US market.]]></description>
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        <title><![CDATA[Biosimilar Trastuzumab Emtansine Shows Consistent PFS in HER2-Positive Breast Cancer]]></title>
        <link>https://www.centerforbiosimilars.com/view/biosimilar-trastuzumab-emtansine-shows-consistent-pfs-in-her2-positive-breast-cancer</link>
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        <pubDate>Fri, 20 Feb 2026 14:52:09 +0000</pubDate>
        <description><![CDATA[Real-world India data show trastuzumab emtansine biosimilars deliver meaningful PFS and manageable safety in heavily pretreated HER2+ metastatic breast cancer.]]></description>
        <media:credit role="publishing company">Center for Biosimilars</media:credit>
        <guid>https://www.centerforbiosimilars.com/rss/biosimilar-trastuzumab-emtansine-shows-consistent-pfs-in-her2-positive-breast-cancer</guid>
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        <title><![CDATA[FDA Approves Filkri, Accord BioPharma’s Short-Acting Filgrastim Biosimilar for Neutropenia]]></title>
        <link>https://www.centerforbiosimilars.com/view/fda-approves-filkri-accord-biopharma-s-short-acting-filgrastim-biosimilar-for-neutropenia</link>
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        <pubDate>Wed, 18 Feb 2026 19:25:00 +0000</pubDate>
        <description><![CDATA[FDA approval of Filkri expands Accord’s G-CSF biosimilar portfolio, offering a short-acting option for neutropenia in cancer care.]]></description>
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        <guid>https://www.centerforbiosimilars.com/rss/fda-approves-filkri-accord-biopharma-s-short-acting-filgrastim-biosimilar-for-neutropenia</guid>
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        <title><![CDATA[Danish Registry Analysis Finds Consistent Safety After Switching to Infliximab Biosimilar GP1111]]></title>
        <link>https://www.centerforbiosimilars.com/view/danish-registry-analysis-finds-consistent-safety-after-switching-to-infliximab-biosimilar-gp1111</link>
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        <pubDate>Tue, 03 Feb 2026 14:00:00 +0000</pubDate>
        <description><![CDATA[New Danish registry data confirm the safety of switching to infliximab biosimilars, showing low rates of serious adverse events in patients with inflammatory arthritis.]]></description>
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        <guid>https://www.centerforbiosimilars.com/rss/danish-registry-analysis-finds-consistent-safety-after-switching-to-infliximab-biosimilar-gp1111</guid>
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        <title><![CDATA[Q&A With Chelsee Jensen, PharmD: FDA Policy Shifts, Biosimilar Development Hurdles, and Market Access in 2026]]></title>
        <link>https://www.centerforbiosimilars.com/view/q-a-with-dr-chelsee-jensen-fda-policy-shifts-biosimilar-development-hurdles-and-market-access-in-2026</link>
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        <pubDate>Mon, 02 Feb 2026 17:45:00 +0000</pubDate>
        <description><![CDATA[Mayo Clinic’s Chelsee Jensen, PharmD, discusses FDA policy changes, biosimilar development hurdles, denosumab lessons, and payer access strategies.]]></description>
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        <title><![CDATA[Early Evidence Supports KM118 as a Biosimilar to Reference Pertuzumab]]></title>
        <link>https://www.centerforbiosimilars.com/view/early-evidence-supports-km118-as-a-biosimilar-to-reference-pertuzumab</link>
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        <pubDate>Wed, 28 Jan 2026 22:00:20 +0000</pubDate>
        <description><![CDATA[A new study confirms KM118, a proposed biosimilar to pertuzumab, shows pharmacokinetic similarity and safety, paving the way for affordable HER2-positive breast cancer treatments.]]></description>
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        <title><![CDATA[Milestone Approvals, Evolving PBM Models May Redefine the 2026 Biosimilar Landscape]]></title>
        <link>https://www.centerforbiosimilars.com/view/milestone-approvals-evolving-pbm-models-may-redefine-2026-biosimilar-landscape</link>
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        <pubDate>Tue, 27 Jan 2026 16:32:46 +0000</pubDate>
        <description><![CDATA[The US biosimilar market evolves with 90 approvals, significant price drops, and new PBM models enhancing access to cost-effective therapies.]]></description>
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        <title><![CDATA[FDA Draft Guidance on Biosimilars Is a Win for Patients; Now Congress Must Finish the Job]]></title>
        <link>https://www.centerforbiosimilars.com/view/fda-draft-guidance-on-biosimilars-is-a-win-for-patients-now-congress-must-finish-the-job</link>
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        <pubDate>Mon, 26 Jan 2026 22:07:22 +0000</pubDate>
        <description><![CDATA[]]></description>
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        <guid>https://www.centerforbiosimilars.com/rss/fda-draft-guidance-on-biosimilars-is-a-win-for-patients-now-congress-must-finish-the-job</guid>
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        <title><![CDATA[Biosimilar Competition Linked to Lower Out-of-Pocket Costs for Medicare Patients]]></title>
        <link>https://www.centerforbiosimilars.com/view/biosimilar-competition-linked-to-lower-out-of-pocket-costs-for-medicare-patients</link>
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        <pubDate>Wed, 21 Jan 2026 19:54:04 +0000</pubDate>
        <description><![CDATA[Biosimilar competition significantly reduces out-of-pocket costs for Medicare patients, enhancing affordability for biologic therapies and improving access.]]></description>
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        <title><![CDATA[Perceptions Still Play a Central Role in Biosimilar Insulin Switching]]></title>
        <link>https://www.centerforbiosimilars.com/view/perceptions-still-play-a-central-role-in-biosimilar-insulin-switching</link>
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        <pubDate>Tue, 20 Jan 2026 22:01:09 +0000</pubDate>
        <description><![CDATA[Explore the complexities of insulin biosimilars, their safety, and the impact on diabetes management in global health systems.]]></description>
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        <guid>https://www.centerforbiosimilars.com/rss/perceptions-still-play-a-central-role-in-biosimilar-insulin-switching</guid>
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        <title><![CDATA[Trial Data Support Equivalence of Denosumab Biosimilar in Postmenopausal Osteoporosis]]></title>
        <link>https://www.centerforbiosimilars.com/view/trial-data-support-equivalence-of-denosumab-biosimilar-in-postmenopausal-osteoporosis</link>
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        <pubDate>Fri, 16 Jan 2026 13:37:46 +0000</pubDate>
        <description><![CDATA[Denosumab biosimilars enhance treatment access for postmenopausal osteoporosis, demonstrating equivalent efficacy and safety to reference products in recent trials.]]></description>
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        <title><![CDATA[What Australia’s Experience Reveals About Biosimilar Adoption and Pricing]]></title>
        <link>https://www.centerforbiosimilars.com/view/what-australia-s-experience-reveals-about-biosimilar-adoption-and-pricing</link>
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        <pubDate>Thu, 15 Jan 2026 19:07:39 +0000</pubDate>
        <description><![CDATA[Australia's biosimilar adoption significantly reduces biologic medicine costs, enhancing access while maintaining utilization amid tighter health care budgets.]]></description>
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        <title><![CDATA[Eye on Pharma: Global Approvals, Launches, and Strategic Partnerships]]></title>
        <link>https://www.centerforbiosimilars.com/view/eye-on-pharma-global-approvals-launches-and-strategic-partnerships</link>
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        <pubDate>Mon, 12 Jan 2026 19:25:24 +0000</pubDate>
        <description><![CDATA[]]></description>
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        <title><![CDATA[Real-World Study Finds Stable Vision After Switch to Ranibizumab Biosimilar]]></title>
        <link>https://www.centerforbiosimilars.com/view/real-world-study-finds-stable-vision-after-switch-to-ranibizumab-biosimilar</link>
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        <pubDate>Wed, 07 Jan 2026 17:26:26 +0000</pubDate>
        <description><![CDATA[Switching from aflibercept to ranibizumab biosimilars maintains stability in nAMD treatment, offering a cost-effective solution for long-term management.]]></description>
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        <title><![CDATA[Evidence Supports Safe, Effective Switching to Etanercept Biosimilars]]></title>
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        <pubDate>Tue, 06 Jan 2026 19:33:57 +0000</pubDate>
        <description><![CDATA[Explore the safety and efficacy of switching to etanercept biosimilars, backed by clinical trials and real-world evidence for chronic inflammatory diseases.]]></description>
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        <title><![CDATA[FDA Approves Amneal Denosumab Biosimilars, Capping Year of Market Expansion]]></title>
        <link>https://www.centerforbiosimilars.com/view/fda-approves-amneal-denosumab-biosimilars-capping-year-of-market-expansion</link>
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        <pubDate>Tue, 06 Jan 2026 12:00:00 +0000</pubDate>
        <description><![CDATA[FDA approves new denosumab biosimilars, enhancing treatment options for osteoporosis and bone metastases while driving competition and cost savings.]]></description>
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