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Japanese year-end approvals include Eliquis, Ryzodeg and Cimzia

 
• By Ian Haydock

Bristol-Myers Squibb's novel anticoagulant Eliquis (apixaban 2.5mg tablet) has been approved in Japan for the prevention of ischemic stroke and systemic embolism in patients with non-valvular atrial fibrillation, setting the stage for a market showdown with Bayer's Xarelto (rivaroxaban) and Boehringer Ingelheim's Prazaxa (dabigatran) in this setting.

Bristol-Myers Squibb's novel anticoagulant Eliquis (apixaban 2.5mg tablet) has been approved in Japan for the prevention of ischemic stroke and systemic embolism in patients with non-valvular atrial fibrillation, setting the stage for a market showdown with Bayer's Xarelto (rivaroxaban) and Boehringer Ingelheim's Prazaxa (dabigatran) in this setting.

The Japanese regulatory clearance for the BMS oral direct Factor Xa inhibitor comes hot on the heels of the EU...

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Viking Rapidly Advancing Oral And Injectable VK2735 For Obesity

 
• By Joseph Haas

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Obesity Beyond GLP-1s: Amylins – The Next Frontier

 
• By Aakash Babu

In this series of articles, we look at different mechanisms of actions beyond GLP-1s that could determine the obesity drug landscape in the coming years. First on our list – amylin receptor agonists, which analysts expect to grow into a $50bn market opportunity.

In Brief: Kezar Plots Lupus Revival For Zetomipzomib As FDA Lifts Hold On Hepatitis Trial

 
• By Manas Mishra

The go-ahead to resume a trial for its only drug candidate, zetomipzomib, in hepatitis could give Kezar a glimmer of hope of reviving another halted study in lupus nephritis.

Kailera Eyes Global Obesity Market With Hengrui’s Phase III Dual Agonist

 
• By Joseph Haas

With China’s Hengrui reporting successful Phase III data for its dual GLP-1/GIP agonist, licensee Kailera is readying plans to demonstrate better efficacy than current obesity drugs.

More from Therapeutic Category

GSK’s Blenrep US Setback Could Go From Bad To Worse

 
• By Sushmita Panda

With a US approval any time soon now looking unlikely, analysts are revising Blenrep’s peak sales guidance downwards.

Boehringer Ingelheim Expects Two Key Approvals In Second Half Of 2025

 
• By Andrew McConaghie

The privately held German pharma firm is hoping to bring a new generation of pulmonary fibrosis and cancer drugs to market but their commercial success is not yet a certainty.

More Pressure on Elevidys As The EU’s CHMP Says ‘No’

 
• By Alexandra Shimmings

Just days after Roche stopped shipments of the DMD gene therapy following safety concerns raised by two patient deaths, its EU approval application has hit a block.