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Sandoz Reveals European Natalizumab Launch Amid GLP-1 Ambitions

European Commission Approval Last Year Promised H1 2024 Roll-Out For MS Treatment

 
• By Dean Rudge

Sandoz arrived in California for its first J.P. Morgan Annual Healthcare Conference as an independent company. As well as revealing its first natalizumab biosimilar launch, the firm spoke at length about how it will look to capitalize on the growing GLP-1 market in the years ahead.

Rocket takes off in the starry sky. Spaceship begins the mission. Space shuttle taking off on a Planet Mars.
• Source: Shutterstock

Sandoz’s Polpharma Biologics-partnered Tyruko (natalizumab) biosimilar to Tysabri has begun shipping in Norway following a successful tender bid for the multiple sclerosis treatment, the company has disclosed at the J.P. Morgan Annual Healthcare Conference currently taking place in San Francisco, California.

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More from Biosimilars

Sandoz Slims Down Pembrolizumab Trial As Regulators Streamline Requirements

 
• By Dave Wallace

As Sandoz continues development of its planned pembrolizumab biosimilar rival to Keytruda, the company has revealed plans to slim down its Phase III trial amid the latest moves from regulators towards streamlining clinical study requirements for biosimilar registration.

Amgen’s Aflibercept Starts Strong As Regeneron Counts Cost Of Eylea Competition

 
• By Dean Rudge

Amgen told investors during its 1 May first-quarter earnings call that its Pavblu biosimilar to Eylea 2mg had flown out of the gates, while Regeneron admitted “some difficult news related to our retinal franchise.”

BGMA Becomes Medicines UK

 
• By Dave Wallace

The UK generics and biosimilars industry will now be represented by Medicines UK, the new name for the former British Generic Manufacturers Association.

J&J Denied Injunction Over Private-Label Ustekinumab In US

 
• By Dave Wallace

Stelara originator J&J has been denied in its initial attempt to prevent Samsung Bioepis and ustekinumab biosimilar partner Sandoz from selling a private-label version of the product through a PBM in the US.

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J&J Denied Injunction Over Private-Label Ustekinumab In US

 
• By Dave Wallace

Stelara originator J&J has been denied in its initial attempt to prevent Samsung Bioepis and ustekinumab biosimilar partner Sandoz from selling a private-label version of the product through a PBM in the US.

UK Forxiga SPCs Wiped Out As Trio Succeed With Plausibility Attack

 
• By Dean Rudge

Generic competition to AstraZeneca’s blockbuster SGLT2 inhibitor Forxiga (dapagliflozin) treatment for diabetes may hit England and Wales earlier than 2028 after a pair of SPCs were invalidated following proceedings initiated by a trio of generics manufacturers.

What’s Next? Five Things To Look Out For In May

 
• By Dean Rudge

Generics Bulletin previews the most noteworthy and anticipated events for May 2025.