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‘The Right Call:’ Australia’s PBAC Addresses ‘Unprecedented’ Backlog With Extra Meeting

‘The Right Call:’ Australia’s PBAC Addresses ‘Unprecedented’ Backlog With Extra Meeting

The government’s decision for the Pharmaceutical Benefits Advisory Committee to hold an extra meeting in 2025 has been welcomed by Medicines Australia, which says that Australians already wait on average 466 days from the time a medicine is approved to when it is subsidized.

Australian Industry Strikes Deal On Deferred PBS Submissions, Challenges Govt's Capacity Claim

Australian Industry Strikes Deal On Deferred PBS Submissions, Challenges Govt's Capacity Claim

Medicines Australia has expressed skepticism over the Pharmaceutical Benefits Advisory Committee’s claim that in March 2025 it will only be able to assess 32 submissions from companies that want to get their drugs subsidized under the Pharmaceutical Benefits Scheme.

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

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.

Nordic Medtech Experts Urge More Collaboration On Health Technology Assessments

Nordic Medtech Experts Urge More Collaboration On Health Technology Assessments

European cross-country HTA collaborations have much to learn from each other to keep prices from rising unfairly, Nordic health technology assessment experts say, adding that talks on collaboration are also ongoing with HTA bodies outside the continent.

Cross-Country HTA Collaboration To Focus On Health Economics & RWE

Cross-Country HTA Collaboration To Focus On Health Economics & RWE

European cross-country HTA collaborations have much to learn from each other to keep drug prices from rising unfairly, Nordic health technology assessment experts say, adding that talks on collaboration are also ongoing with HTA bodies outside the continent.

Despite Landing Biggest PBM Formularies, Celltrion’s Zymfentra Not Listed By US Insurers

Despite Landing Biggest PBM Formularies, Celltrion’s Zymfentra Not Listed By US Insurers

Celltrion gave updates on several business aspects and reassured its shareholders that the delayed insurance listing for Zymfentra will not affect its set annual sales goal.

New Pharma Research Law Fails To Make Germany More Competitive Says EUCOPE Head

New Pharma Research Law Fails To Make Germany More Competitive Says EUCOPE Head

Germany’s Medical Research Act clears its final legal hurdle after federal council sign off.

Drug Repurposing Firm Every Cure Bags $60m Investment

Drug Repurposing Firm Every Cure Bags $60m Investment

Backed by AI and former FDA official Janet Woodcock, Every Cure is set to identify approved drugs for patients who don’t have treatment options around the world.

New German Research Law Fails To Stop Companies From Opting Out Of The Market

New German Research Law Fails To Stop Companies From Opting Out Of The Market

Germany’s Medical Research Act has cleared its final legal hurdle after the federal council signed it off.

EU Authority Mulls Paying For  Late-Stage Research As A Pull Incentive For Neglected Disease Drugs

EU Authority Mulls Paying For Late-Stage Research As A Pull Incentive For Neglected Disease Drugs

It is time for a much greater focus on pull incentives to ensure viable market conditions for medicines for neglected diseases that are traditionally regarded as unprofitable.