HTA must consider health equity for progress

By HEOR Staff Writer

March 24, 2023

ICER has released a White Paper on Health Equity. This paper measures the impact of health technology assessment (HTA) on equity, and suggests approaches to leverage HTA to advance health equity for racial, ethnic, and socially disadvantaged groups.

When decision-makers evaluate data to inform pricing and insurance coverage, they must consider the implications for health equity. They have taken a close look at every step of our work to assess if we and other HTA groups can make improvements and will enhance the discussion on clinical trial diversity.

It is essential for HTA bodies to be aware of how to add equity into the methods of health technology assessment, and if that can be accomplished by utilizing innovative methods that are expansions of traditional cost-effectiveness analyses, through evidence-grounded deliberative approaches, or a combination of the two.

Reference url

Recent Posts

Belgium Fast Access Medicines
Belgium Fast Access Medicines Revolutionize Treatment for IgA Nephropathy

By João L. Carapinha

July 1, 2026

Belgium Fast Access Medicines has moved from policy to practice. Authorities have granted temporary reimbursement to Atrasentan, the first therapy approved under the new Early and Equitable Fast Access procedure, offering quicker hope to patients with IgA nephropathy while anchoring the country’s...
Retracted Trial Publication
Retracted Trial Publication Undermines Support for Avacopan in AAV Treatment

By João L. Carapinha

July 1, 2026

The Retracted Trial Publication of the ADVOCATE study has eliminated the central evidence that supported approval of Tavneos (avacopan) for severe active anti-neutrophil cytoplasmic autoantibody-associated vasculitis (AAV). At the request of two lead academic authors, the
regulatory validation taletrectinib
Advancing Regulatory Validation Taletrectinib for Enhanced NSCLC Treatment

By João L. Carapinha

June 30, 2026

The MHRA’s validation of Nuvation Bio’s marketing authorisation application marks an important regulatory validation taletrectinib for adults with advanced ROS1-positive non-small cell lung cancer. This milestone, achieved via the International Recognition Procedure in parallel with EMA review, f...