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Published on: May 4, 2017
Evidence That Regulatory And Market Forces Are Driving Adoption Of Biosimilars
Janice Jhang1, Troyen A Brennan2
1Janice Jhang (janicejhang@g.harvard.edu), Harvard University, Cambridge, Massachusetts.
The US biosimilar market, initially disappointing, is now flourishing, offering opportunities to reduce biologic drug costs. Policy interventions can further accelerate biosimilar adoption and affordability.
Area of Science:
- Health Economics
- Pharmaceutical Policy
- Biotechnology
Background:
- The US biosimilar market has underperformed since its inception, raising concerns about its future.
- Biosimilars offer a critical pathway to manage rising biologic drug expenditures and enhance medication accessibility.
- Understanding market dynamics across different drug classes and financial stakeholders is crucial.
Purpose of the Study:
- To evaluate the evolution and current state of the US biosimilar market.
- To identify factors contributing to market performance and future viability.
- To examine policy and market dynamics through a case study.
Main Methods:
- Review of medication class distinctions and financial stakeholder involvement.
- Analysis of recent evidence on the post-approval biosimilar marketplace.
- Case study analysis of adalimumab biosimilar entry and market impact.
Main Results:
- Despite early challenges, the US biosimilar market is showing signs of maturation and growth.
- The introduction of biosimilars for adalimumab illustrates evolving market and policy trends.
- Evidence suggests a flourishing post-approval biosimilar landscape.
Conclusions:
- The US biosimilar market is evolving positively, with increasing signs of success.
- Policy makers can leverage regulatory and payment strategies to further boost biosimilar uptake.
- Accelerating biosimilar adoption is key to controlling healthcare costs and improving patient access to essential medicines.
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