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Biosimilar

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February 10, 2021
3 min read
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Biosimilar uptake varies by drug class, practice type, hospital ownership status

Biosimilar uptake varies by drug class, practice type, hospital ownership status

Biosimilar use among Medicare fee-for-service beneficiaries seems to depend most on practice setting and hospital ownership status, with few patient or physician characteristics linked to usage, according to data in JAMA Network Open.

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December 26, 2020
1 min read
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Community Oncology Alliance elects 2021 president

Community Oncology Alliance elects 2021 president

Kashyap Patel, MD, has been elected president of Community Oncology Alliance, a nonprofit advocacy group that serves community oncology practices and their patients.

News
December 17, 2020
1 min read
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FDA approves Riabni, third biosimilar to Rituxan

The FDA approved rituximab-arrx for multiple indications.

News
October 09, 2020
3 min read
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Should prices of biosimilars be regulated in the US?

Should prices of biosimilars be regulated in the US?

Bringing down the prices of biosimilars in the United States will be a tricky balance. On one hand, you want to be able to make these drugs available to every patient who needs them. On the other hand, just lowering the prices artificially through legislation could stunt innovation and disincentivize companies from bringing these drugs to market.

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October 09, 2020
14 min read
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Greater uptake, education needed to realize cost-saving potential of biosimilars

Greater uptake, education needed to realize cost-saving potential of biosimilars

More than 5 years after the first FDA approval of a biosimilar, the U.S. health care system has yet to realize the full potential of these products to reduce drug costs and increase access to hematology/oncology treatments.

News
July 27, 2020
1 min read
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European Commission expands approved indications for subcutaneous infliximab biosimilar

European Commission expands approved indications for subcutaneous infliximab biosimilar

The European Commission has extended approval for Celltrion Healthcare’s subcutaneous infliximab biosimilar to treat adults with ankylosing spondylitis, Crohn’s disease, ulcerative colitis, psoriatic arthritis and psoriasis.

News
July 17, 2020
2 min read
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Biosimilar uptake still limited in the U.S.

Biosimilar uptake still limited in the U.S.

The European Medicines Agency approved the first biosimilar in Europe in 2006. It was almost 10 years before the United States followed. Despite potential savings for payers and patients, biosimilar uptake in the U.S. remains limited.

News
July 10, 2020
5 min read
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Bringing drug costs down a ‘peg’ or two

Bringing drug costs down a ‘peg’ or two

At our center, metrics obtained through our participation in CMS’s Oncology Care Model have allowed us to improve patient experience scores, reduce ED utilization and hospital admission, and impact several other measures of quality care.

News
July 09, 2020
1 min read
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FDA approves Hulio, sixth Humira biosimilar

FDA approves Hulio, sixth Humira biosimilar

The FDA has approved the sixth biosimilar to adalimumab, adalimumab-fkjp, for all eligible indications of the biologic product, according to a company press release.

News
July 02, 2020
2 min read
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Appeals court upholds Amgen victory in Enbrel fight; Sandoz eyes Supreme Court

Appeals court upholds Amgen victory in Enbrel fight; Sandoz eyes Supreme Court

A U.S. appeals court has ruled in favor of two patents for Amgen’s etanercept against the biosimilar etanercept-szzs from Novartis’ Sandoz, upholding a prior decision validating claims of patent infringement.

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