Recommendations for biomarker data collection in clinical trials by longevity biotechnology companies
Biomarkers of aging have the potential to transform geroscience clinical trials because of their broad applications in stratifying participants, prioritizing interventions, and monitoring responses to geroprotectors. As longevity biotechnology companies (LBCs) continue to plan and launch innovative clinical trials, standard practices in collecting data and applying biomarkers of aging will allow the field to support parallel and ongoing validation and benchmarking efforts for aging biomarkers. Moreover, defining best practices will ensure future reuse of valuable clinical data through pre-competitive alignment on shared tools. Here, we propose recommendations for such collections. We believe that wide adoption of these recommendations will allow LBCs to produce and leverage the highest quality data from their clinical trials, while also benefiting the geroscience field more broadly with minimal additional effort.
Authors
- James Peyer
- Jesse R. Poganik (ORCID: https://orcid.org/0000-0003-3098-8550)
- Nir Barzilai (ORCID: https://orcid.org/0000-0002-7787-6268)
- Nicola Boekstein (ORCID: https://orcid.org/0000-0003-3269-6498)
- Jim Mellon
- Kristen Fortney (ORCID: https://orcid.org/0000-0002-6008-2170)
- Risa Starr
- Chiara M. S. Herzog
- Mahdi Moqri
Institutions
- Brigham and Women's Hospital (US)
- Albert Einstein College of Medicine (US)
- Harvard University (US)
- King's College London (GB)
- Universität Innsbruck (AT)
- Anoka-Ramsey Community College (US)
- Longevity Biotech (United States) (US)
- Cambrian Innovation (United States) (US)
- Joint BioEnergy Institute (US)
- Stanford University (US)
Publication Details
- Journal
- npj Aging
- Published
- 2025-12-23
- DOI
- https://doi.org/10.1038/s41514-025-00313-1
- Primary Topic
- Genetics, Aging, and Longevity in Model Organisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00