Analysis of predictive value of animal repeated dose toxicity study results for clinical safety of US FDA-approved anticancer drugs between 2019 and 2023
- DOI
- 10.1016/j.yrtph.2026.106031
- Published
- 2026-03
- Container
- Regulatory Toxicology and Pharmacology
- Publisher
- Elsevier BV
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.yrtph.2026.106031,
title = {Analysis of predictive value of animal repeated dose toxicity study results for clinical safety of US FDA-approved anticancer drugs between 2019 and 2023},
author = {Gyeyoung Choi and Seungjin Bae and Kyung-Min Lim},
year = {2026},
journal = {Regulatory Toxicology and Pharmacology},
doi = {10.1016/j.yrtph.2026.106031},
url = {https://doi.org/10.1016/j.yrtph.2026.106031}
}RIS
TY - JOUR TI - Analysis of predictive value of animal repeated dose toxicity study results for clinical safety of US FDA-approved anticancer drugs between 2019 and 2023 AU - Gyeyoung Choi AU - Seungjin Bae AU - Kyung-Min Lim PY - 2026 JO - Regulatory Toxicology and Pharmacology DO - 10.1016/j.yrtph.2026.106031 UR - https://doi.org/10.1016/j.yrtph.2026.106031 ER -
APA
Choi, G., Bae, S., & Lim, K. (2026). Analysis of predictive value of animal repeated dose toxicity study results for clinical safety of US FDA-approved anticancer drugs between 2019 and 2023. Regulatory Toxicology and Pharmacology. https://doi.org/10.1016/j.yrtph.2026.106031
Source records
- crossref · retrieved 2026-09-26T09:51:59.546Z