Bioeq’s Lucentis Biosimilar Is Given EU Go-Ahead

Launch Dates And Financial Terms Of A Marketing Deal With Teva Remain Under Wraps

Bioeq’s Ranivisio ranibizumab biosimilar has gained European Commission authorization for all innovator indications including wet AMD, the leading cause of blindness among over-65s.

Close-up of woman's eye, with light falling on retina
The Ranivisio ranibizumab biosimilar has been formally approved by the European Commission • Source: Shutterstock

Bioeq’s Ranivisio, a ranibizumab biosimilar based on branded original Lucentis, has gained an EU marketing authorization for several serious retinal diseases.

The authorization grants Ranivisio access to markets in all 27 EU member states plus Iceland, Norway, and Liechtenstein. The approval...

More from Biosimilars

Alvotech Focuses On Value Over Volume As Sales Continue To Grow

 
• By 

As Alvotech announced first-half results that outpaced expectations, the biosimilars developer’s management explained that the firm was targeting value and product margin over market share and volumes.

Henlius And Organon Sued In US Over Plans To Market Perjeta Biosimilar

 
• By 

Roche and its Genentech subsidiary have sued Shanghai Henlius Biotech and commercialization partner Organon in the US, alleging infringement of 24 patents covering Perjeta (pertuzumab). The litigation follows Roche’s recent disclosure that biosimilars to Perjeta could launch as soon as 2026.

Accord Takes On Ustekinumab Rivals In US With Steepest Discount Yet

 
• By 

Boasting the “lowest WAC price among branded biosimilars to Stelara”, Accord BioPharma has launched its Imuldosa version of ustekinumab in the US at a 92% discount to the blockbuster immunology brand.

Formycon’s Search For Keytruda Biosimilar Partner Is Key To Deliver FY2025 Guidance

 

With H1 revenues not even hitting double-digits, Formycon is bidding on partnerships and royalties to generate at least €46m over the next half-year to reach its revenue goal.

More from Products

Cingulate Installs Interim Leadership After CEO Put On Administrative Leave

 
• By 

Shortly after filing its lead candidate for ADHD through the FDA’s 505(b)(2) hybrid new drug application pathway, Cingulate has appointed interim leadership after placing chairman and CEO Shane Schaffer on administrative leave over legal matters unrelated to the company.

Henlius And Organon Sued In US Over Plans To Market Perjeta Biosimilar

 
• By 

Roche and its Genentech subsidiary have sued Shanghai Henlius Biotech and commercialization partner Organon in the US, alleging infringement of 24 patents covering Perjeta (pertuzumab). The litigation follows Roche’s recent disclosure that biosimilars to Perjeta could launch as soon as 2026.

Accord Takes On Ustekinumab Rivals In US With Steepest Discount Yet

 
• By 

Boasting the “lowest WAC price among branded biosimilars to Stelara”, Accord BioPharma has launched its Imuldosa version of ustekinumab in the US at a 92% discount to the blockbuster immunology brand.