Biosimilars

IGBA Kicks Off Global Biosimilars Week 2024

IGBA Kicks Off Global Biosimilars Week 2024

 
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Running from 11-14 November, the fifth annual Global Biosimilars Week awareness campaign has been launched by the IGBA, with the international off-patent association this year focusing on advancing access.

Meitheal Brings In Another Three US Biosimilars

Meitheal Brings In Another Three US Biosimilars

 
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Meitheal has announced a licensing agreement with parent company Hong Kong King-Friend to add another three biosimilars to its pipeline for the US market.

Coherus Looks To Put Udenyca Supply Issues In The Rearview Mirror

Coherus Looks To Put Udenyca Supply Issues In The Rearview Mirror

 
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Coherus BioSciences will have to weather the storm of supply interruptions for its sole biosimilar product, Udenyca, in the final quarter of 2024.

‘Imitation Is Flattery,’ Regeneron Tells Amgen As It Prepares To Compete On Eylea

‘Imitation Is Flattery,’ Regeneron Tells Amgen As It Prepares To Compete On Eylea

 
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In the first earnings call since Amgen confirmed launch of the first US biosimilar to Regeneron’s near $6bn Eylea brand, the originator spoke of its confidence in defending its brand, while also touching on how supply issues for repackaged Avastin had impacted its operations.


Alvotech And Advanz Claim A Global First With Golimumab Filing

Alvotech And Advanz Claim A Global First With Golimumab Filing

 
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Alvotech and Advanz have celebrated a worldwide first with the European Medicines Agency’s acceptance of an application for their partnered golimumab biosimilar rival to Simponi.

Amgen Sees Plenty Of Interest In US Eylea Biosimilar, Buoyed By Strong Supply Chain

Amgen Sees Plenty Of Interest In US Eylea Biosimilar, Buoyed By Strong Supply Chain

 
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All eyes are on Eylea, after Amgen said last week that it would launch the first US biosimilar in the face of ongoing litigation. The California-based player has spoken of its prospects in the wet-AMD space, including a desire to chart its own path amid supply shortages for Avastin.

Alvotech Petitions FDA To Deny Interchangeability For Rival Stelara Biosimilars

Alvotech Petitions FDA To Deny Interchangeability For Rival Stelara Biosimilars

 
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In a citizen petition to the FDA, Alvotech has called on the US agency to refrain from approving as interchangeable certain Stelara biosimilars that use a different cell line to its own ustekinumab product – including the Pyzchiva version set to be brought to market by Samsung Bioepis and Sandoz.

Roche, Chugai Weigh In As Tocilizumab Biosimilars Fail To Hit The Mark In Q3

Roche, Chugai Weigh In As Tocilizumab Biosimilars Fail To Hit The Mark In Q3

 
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While Roche admits that an acceleration of biosimilar competition to its blockbuster IL-6 inhibitor Actemra/RoActemra is anticipated in the final three months of the year, the Swiss originator has been surprised by the lack of challenge to its franchise so far.


Sandoz Says Amgen’s At-Risk Aflibercept Launch ‘Doesn’t Change Our Thinking’

Sandoz Says Amgen’s At-Risk Aflibercept Launch ‘Doesn’t Change Our Thinking’

 
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Sandoz has indicated that Amgen’s recently-announced at-risk US launch of a rival to Eylea doesn’t change its thinking around launch timing for its own FDA-approved aflibercept biosimilar.

Teva And Alvotech Add Indications For US Stelara Rival

Teva And Alvotech Add Indications For US Stelara Rival

 
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Alvotech and US marketing partner Teva have celebrated a further approval for their Selarsdi ustekinumab biosimilar rival to Stelara that encompasses a new presentation as well as a label expansion to include adults with Crohn’s disease and ulcerative colitis.

Roche Does Not Feel Eylea Biosimilars Will Change The Status Quo

Roche Does Not Feel Eylea Biosimilars Will Change The Status Quo

 
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Roche’s 2022-launched Vabysmo took no time at all to reach the coveted $1bn in sales, and the originator is continuing to feel optimistic about the newer-generation VEGF brand’s prospects, even as Amgen readies the launch of the first US biosimilar to Eylea.

Alvotech And Fuji File Third Biosimilar Application In Japan

Alvotech And Fuji File Third Biosimilar Application In Japan

 
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Only a month after filing their second biosimilar application with Japanese regulators, Alvotech and Fuji have submitted a further one for an undisclosed biosimilar as part of their local partnership.


Roche Changes Its Tune On 2025 Xolair Biosimilars Amid Celltrion’s First Filing

Roche Changes Its Tune On 2025 Xolair Biosimilars Amid Celltrion’s First Filing

 
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Biosimilar competition to Xolair, one of the largest monoclonal antibodies coming off patent in the middle of this decade, has been pushed back to an unknown date in the US, as Celltrion awaits news from the US FDA on its biosimilar application.

Amgen Will Launch First US Eylea Biosimilar At Risk

Amgen Will Launch First US Eylea Biosimilar At Risk

 
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A watershed moment is on the horizon for US biosimilars, with Amgen looking poised to debut competition to Eylea (aflibercept).

Stelara ‘At The End Of Its Life’ As Biosimilars Put Pressure On J&J

Stelara ‘At The End Of Its Life’ As Biosimilars Put Pressure On J&J

 

With marketed European biosimilar rivals already making a dent in Stelara’s sales performance, Johnson & Johnson mourns its blockbuster’s upcoming loss of exclusivity across the Atlantic Ocean.

Fresenius Offers First And Only Canadian Tocilizumab Biosimilar

Fresenius Offers First And Only Canadian Tocilizumab Biosimilar

 
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Fresenius Kabi has claimed another first for its Tyenne biosimilar rival to Actemra, becoming the debut challenger to the rheumatoid arthritis treatment to launch in Canada.


Accord Follows US Approval With EU Nod On Ustekinumab

Accord Follows US Approval With EU Nod On Ustekinumab

 
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Accord has received a nod from the EMA for its Stelara biosimilar, while Neuraxpharm has seen a buprenorphine hybrid film endorsed and Viatris has received a positive CHMP opinion for an eltrombopag generic.

Formycon Points To Positive Results For Keytruda Biosimilar

Formycon Points To Positive Results For Keytruda Biosimilar

 
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With clinical trials for its FYB206 proposed biosimilar to Keytruda (pembrolizumab) currently ongoing, Formycon has highlighted analytical studies that suggest its version is “structurally and functionally highly similar to the reference product.”

Richter And Bio-Thera Shake Hands On $100m+ European Ustekinumab Deal

Richter And Bio-Thera Shake Hands On $100m+ European Ustekinumab Deal

 
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Gedeon Richter and Bio-Thera Solutions have announced a European licensing deal worth potentially more than $100m for the Chinese biosimilar developer’s BAT2206 proposed rival to Stelara.

Dong-A Makes It Five: Accord Gears Up For US Launch After Ustekinumab Approval

Dong-A Makes It Five: Accord Gears Up For US Launch After Ustekinumab Approval

 
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Partners Dong-A ST and Meiji Seika Pharma have demonstrated their credentials in the US biosimilar market, bagging a US Food and Drug Administration approval for their biosimilar Stelara product that will be commercialized by Accord Healthcare.