Participants in the <scp>FDA</scp>'s Biomarker Qualification Program

The US FDA's Biomarker Qualification Program (BQP) aims to validate biomarkers for use in the therapeutic development process. Applicants to this program are not restricted to just pharmaceutical firms and a variety of incentives may underlie applicants' decision to participate. Of the 80 biomarker qualification programs that were initiated through February 2025, we find that academic organizations (70.0%) are the most common applicants, followed by pharmaceuticals-related industries (55%), government entities (51.25%), and pharmaceutical firms (50%), although much of this activity is in the context of multi-party consortia. With respect to stage of development, all phase-I-related biomarkers are developed in some form of partnership, while academic institutions alone and foundations devote slightly more attention to trial endpoints as a total share of BQP activities. These findings shed light on the incentives at play and the types of stakeholders that have been active in the development of these tools to date.

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Publication Details

Journal
Clinical Pharmacology & Therapeutics
Published
2025-04-09
DOI
https://doi.org/10.1002/cpt.3661
Citations
3
Primary Topic
Biosimilars and Bioanalytical Methods
Type
article
Field-Weighted Citation Impact
2.39

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article

Participants in the FDA's Biomarker Qualification Program

Ariel Dora Stern, Mahnum Shahzad
3 citations
Clinical Pharmacology & Therapeutics
Biosimilars and Bioanalytical Methods
2.39
article

Participants in the FDA's Biomarker Qualification Program

Ariel Dora Stern, Mahnum Shahzad
article en
3 citations

Abstract

The US FDA's Biomarker Qualification Program (BQP) aims to validate biomarkers for use in the therapeutic development process. Applicants to this program are not restricted to just pharmaceutical firms and a variety of incentives may underlie applicants' decision to participate. Of the 80 biomarker qualification programs that were initiated through February 2025, we find that academic organizations (70.0%) are the most common applicants, followed by pharmaceuticals-related industries (55%), government entities (51.25%), and pharmaceutical firms (50%), although much of this activity is in the context of multi-party consortia. With respect to stage of development, all phase-I-related biomarkers are developed in some form of partnership, while academic institutions alone and foundations devote slightly more attention to trial endpoints as a total share of BQP activities. These findings shed light on the incentives at play and the types of stakeholders that have been active in the development of these tools to date.

Clinical Pharmacology & TherapeuticsVol. 118(1)
Harvard University (US), Hasso Plattner Institute (DE), University of Potsdam (DE), Harvard Pilgrim Health Care (US)
Novo Nordisk Fonden
Partnerships for the goals
Openalex Percentile: Top 12%
Biosimilars and Bioanalytical Methods
2.39
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