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Cost Effectiveness

GLP-1s For Obesity: Maximalists, Skeptics And ‘No Sales Targets’

GLP-1s For Obesity: Maximalists, Skeptics And ‘No Sales Targets’

A high-profile panel that included a senior executive from F-Prime Capital, Novo Nordisk's India chief and a leading endocrinologist discussed, at a recent event, some of the big opportunities, challenges and transformational trends underway as obesity drugs take the world by storm.

EU Acknowledges Demand For Psychedelic Drug Development Progress: One Million Signatures Now Needed

EU Acknowledges Demand For Psychedelic Drug Development Progress: One Million Signatures Now Needed

The European Commission has registered a European citizens' initiative that explains how the EU can foster equitable, timely, affordable, safe and legal access to innovative psychedelic-assisted treatments. Work towards securing the one million signatures needed for the next step is starting soon.

Australia Considers New 'Bridging Fund' Among 50 Recommendations For HTA Reform

Australia Considers New 'Bridging Fund' Among 50 Recommendations For HTA Reform

Industry says it is ready to work with the government on the recommendations from a major review of Australia’s health technology assessment system that covers areas such as discount rate reductions and setting up a separate budgetary allocation to temporarily subsidize access to certain drugs.

Spain Consults On Plans To Regulate HTAs

Spain Consults On Plans To Regulate HTAs

New rules on health technology assessments in Spain make room for real-world evidence and early dialogue.

US FDA’s Marks Issues ‘Provocative’ Call For Target Gene Therapy Profile That Includes Costs

US FDA’s Marks Issues ‘Provocative’ Call For Target Gene Therapy Profile That Includes Costs

CBER Director Peter Marks said recent leaps in gene therapy science have not been matched by more affordable manufacturing technology and that the field needs to set a cost-effectiveness target. 

English HTA Finally Greenlights Conditional Funding for MSD’s Welireg

English HTA Finally Greenlights Conditional Funding for MSD’s Welireg

MSD welcomes the decision but says the drug should have gone through NICE’s Highly Specialized Technologies route that allows more flexibility regarding uncertainty around rare disease drugs.

England’s Cost Effectiveness Rejection Is Another Setback For Eisai And Biogen’s Leqembi

England’s Cost Effectiveness Rejection Is Another Setback For Eisai And Biogen’s Leqembi

Cost watchdog NICE has blocked Leqembi’s use, but a pricing deal could unlock access to the beta-amyloid targeting drug

Use AI In Health Technology Assessments Only When Valuable, England’s NICE Tells Pharma Firms

Use AI In Health Technology Assessments Only When Valuable, England’s NICE Tells Pharma Firms

Pharmaceutical companies should only use AI in evidence generation and reporting where there is “demonstrable value from doing so,” according to England’s health technology assessment body, NICE.

Leqembi's UK Rollercoaster: A Yes From MHRA, A No From NICE

Leqembi's UK Rollercoaster: A Yes From MHRA, A No From NICE

While the drug regulator has approved Eisai/Biogen’s early Alzheimer’s disease treatment, the health technology assessment institute is worried that its benefits are too small to justify its costs – a concern that Eisai has pledged to address.

England Lags Behind Eight European Countries On Innovative Drug Availability

England Lags Behind Eight European Countries On Innovative Drug Availability

In this third article of a series on new drug reimbursement recommendations by the HTA body NICE, the Pink Sheet finds that fewer innovative medicines are reimbursed in England than in eight other European nations.