Unlocking the Value of Biosimilars: Challenges and Solutions

By HEOR Staff Writer

August 10, 2023

The International Society for Pharmacoeconomics and Outcomes Research (ISPOR) has recently published a report highlighting the gaps and challenges in the value assessment of biosimilars.

The report brings to light the ongoing debate on how to accurately assess the value of biosimilars, especially when they request reimbursement for the same indication as the reference biologic. The report also touches upon the different regulatory requirements for biosimilars across various jurisdictions.

The aim of this review is to provide an overview of the existing challenges and propose potential approaches to address them. This could pave the way for improved methodologies in economic evaluation and better access to these therapies in different jurisdictions.

Assessing the value of a biosimilar, a biological product highly similar to an already approved biological product, can be done through either a price comparison or a full economic evaluation. The choice of method depends on factors such as the relative efficacy of the reference biologic and the biosimilar, indication extrapolation, and value assessment in biologic-naive and biologic-experienced patients. A price comparison is typically used when the two products differ significantly in terms of costs, but not effectiveness. However, a full economic evaluation is required when the reference biologic is not reimbursed, has not been appraised, or is not the standard of care. Some countries, such as Belgium, France, and the Netherlands, classify biosimilars as products with no added therapeutic value compared to the reference biologic. Therefore, they have implemented an abbreviated pricing and reimbursement pathway for biosimilars. The value assessment of a biosimilar is a dynamic process and may need to be revisited as new evidence emerges.

The ISPOR Special Interest Group on Biosimilars is committed to generating new insights in this field by interviewing experts at Health Technology Assessment (HTA) agencies worldwide.

For the full report follow the link below.

Reference url

Recent Posts

Enhertu Breast Cancer Treatment Gains FDA Approval in Neoadjuvant and Adjuvant Settings

By João L. Carapinha

May 18, 2026

Enhertu breast cancer treatment has secured FDA approval for neoadjuvant use in adults with HER2-positive Stage II or III disease before surgery, followed by taxane plus trastuzumab and pertuzumab, and for adjuvant therapy in patients with residual invasive disease after prior trastuzumab-based r...
Pharmaceutical Onshoring Agreements: Navigating Tariff Relief and National Security Policies
The US Bureau of Industry and Security published formal procedures enabling manufacturers of patented pharmaceutical products to apply for company-specific pharmaceutical onshoring agreements with the Department of Commerce. These agreements allow qualifying firms to secure a reduced Section 232 ...
NICE Approves Durvalumab for Gastric Cancer Treatment

By HEOR Staff Writer

May 15, 2026

NICE has issued final draft guidance recommending durvalumab, within its marketing authorisation, for use with 5-fluorouracil, leucovorin, oxaliplatin and docetaxel (FLOT) chemotherapy as neoadjuvant and adjuvant treatment, followed by durvalumab monotherapy as adjuvant treatment, in adults with ...