Report reveals fall in biomarker approval volumes
Amplion Research's latest report looks at approval trends for biomarker-based IVD tests in the US.
There has been a decline in the number of approvals of new biomarker-based in vitro diagnostic (IVD) tests, according to a new report by Amplion Research.
The research firm's latest publication, entitled 'Approval Trends for Biomarker-Based IVD Tests: Realizing the Promise of Personalized Medicine', reveals that annual approvals have fallen over the last five years, despite widespread interest in biomarker-based testing.
Amplion Research gives a number of contributing factors for the trend, such as the lengthy and ever-growing FDA review periods for these tests.
In addition, the validation process for biomarkers for commercial use is long and costly, while some tests are not reviewed by the FDA as they are marketed as services.
John Audette, president of Amplion Research, observed: "The FDA has difficult and often competing mandates in maintaining public safety while facilitating advancements in healthcare.
"Without further analysis it is impossible to say conclusively what role FDA review periods are having on biomarker-based test approval rates, but ensuring that FDA has adequate resources may indeed be a key factor in advancing personalised medicine."
Related News
-
News Swiss pharma industry warns US tariffs could harm global patient care
The Swiss pharmaceutical sector has raised alarms over new US tariffs on medicines, warning of disrupted supply chains, increased costs, and delayed innovation, all of which could jeopardise patient access to essential treatments worldwide.
-
News Women in Pharma: CPHI India – India’s Pharmaceutical Industry and Gender Inclusion Challenges
India’s pharmaceutical industry has emerged as a significant player in the global market, valued at USD 50 billion in FY 2023-2024, according to Frost & Sullivan’s analysis. This sector encompasses a diverse portfolio, including drugs, vacc... -
News Biogen acquires Apellis Pharmaceuticals to boost immunology and rare disease profile
Biogen Inc. has announced its acquisition of Apellis Pharmaceuticals, Inc., a move that is set to significantly enhance its growth portfolio in immunology and rare diseases. The agreement, valued at approximately US$5.6 billion, will see Biogen purchas... -
News Gilead Sciences acquires Ouro Medicines for over US$2 billion
Gilead Sciences confirms a deal to take over Ouro Medicines, adding to a portfolio of therapies for autoimmune diseases.
-
News Women in Pharma: Advancing Women's Health
Discover the latest innovations in technologies and therapeutics that are revolutionising women's health in our latest CPHI Online Women in Pharma infographic.
-
News CPHI Pharma Awards 2026: Recognising Excellence in an Evolving Industry
Submissions now open — deadline May 16
-
News Dr Reddy's to launch generic semaglutide in India
Dr Reddy’s Laboratories, one of India’s leading pharmaceutical companies, is preparing to launch a generic version of semaglutide, branded as Obeda, in March. Obeda is expected to provide a more affordable alternative to Ozempic a... -
News Frontier Biotech and GSK Forge RNA Therapy Partnership
Frontier Biotechnologies and GSK have entered a global licensing agreement to advance small interfering RNA (siRNA) therapeutics. This collaboration grants GSK exclusive rights to develop and commercialise two promising siRNA candidates, marking a mile...