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BioWorld - Sunday, March 22, 2026
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BioWorld, Regulatory
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CMS begins to tear down the wall to value-based Rx pricing

June 18, 2020
By Mari Serebrov
After 30 years of following the same rules to ensure Medicaid receives the lowest price available for prescription drugs, the U.S. Centers for Medicare & Medicaid Services (CMS) is starting to adapt those rules for the 21st century.
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Tazverik product image

Back for seconds, Epizyme served up FDA go-ahead for Tazverik in FL

June 18, 2020
By Randy Osborne
About six months after Epizyme Inc. won FDA clearance of Tazverik (tazemetostat) for epithelial sarcoma (ES), the firm scored accelerated approval in the larger indication of relapsed or refractory (r/r) follicular lymphoma (FL). Specifically, U.S. regulators cleared the methyltransferase inhibitor for adults whose tumors test positive for an EZH2 mutation who have received at least two prior systemic therapies and for those with no satisfactory alternative treatment options – language that “gives physicians a lot of flexibility to use their clinical judgement in how to best prescribe” the drug, CEO Robert Bazemore noted.
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Regulatory front for June 18, 2020

June 18, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory actions for June 18, 2020

June 18, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aligos, Beigene, Cynata, Dicerna, Epizyme, Hutchison, Linnaeus, Pear, Protagonist, TFF, Ultragenyx.
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Catching up with EMA, FDA grants Ilaris new Still's disease indication

June 17, 2020
By Michael Fitzhugh
Four years after the EMA first approved Novartis AG's Ilaris (canakinumab) for the treatment of adult-onset Still’s disease (AOSD), the FDA has followed suit, giving it a green light in the indication following a priority review. The rare rheumatic condition usually affects younger adults and can occur as infrequently as once, but also intermittently or chronically.
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FDA icons

Back to ‘normal’? FDA adcom meets, but questions loom over others

June 17, 2020
By Mari Serebrov
In a step toward what may become the new normal, at least for now, the Pediatric Oncology Subcommittee of the FDA’s Oncologic Drugs Advisory Committee is meeting virtually Wednesday and Thursday to review pediatric development plans for four cancer drugs.
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Regulatory front for June 17, 2020

June 17, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory actions for June 17, 2020

June 17, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aclaris, Curevac, Foundation Medicine, Hookipa, Ipsen, Kamada, Merck, Nanobiotix, Novartis, PTC, Reneuron, TG.
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Regulatory actions for June 16, 2020

June 16, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Akili, Arch, Edesa, Eli Lilly, Jazz, Valeo.
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Regulatory front for June 16, 2020

June 16, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Amgen, Esperion, Gilead, Lilly, Merck, Novartis.
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