Value and Implementation of the Aggregate Safety Assessment Plan
- PMID: 37072647
- DOI: 10.1007/s40290-023-00470-2
Value and Implementation of the Aggregate Safety Assessment Plan
Abstract
Aggregate safety assessment involves evaluation of the totality of safety data to characterize the emerging safety profile of a product. The Drug Information Association-American Statistical Association Interdisciplinary Safety Evaluation scientific working group recently published an approach to developing an Aggregate Safety Assessment Plan (ASAP). Creation of an ASAP facilitates a consistent approach to safety data collection and analysis across studies and minimizes important missing data at the time of regulatory submission. A critical aspect of the ASAP is identification of the Safety Topics of Interest (STOI). The STOI, as defined in the ASAP, comprises adverse events (AEs), which have the potential to impact the benefit: risk profile of a product and typically require specialized data collection or analyses. While there are clear benefits to developing an ASAP for a drug development program, multiple concerns may be encountered with implementation. This article uses the examples of two STOIs to demonstrate the benefits and efficiencies gained with implementation of the ASAP in safety planning as well as in optimally characterizing the emerging safety profile of a product.
© 2023. The Author(s), under exclusive licence to Springer Nature Switzerland AG.
Similar articles
-
Aggregate Safety Assessment Planning for the Drug Development Life-Cycle.Ther Innov Regul Sci. 2021 Jul;55(4):717-732. doi: 10.1007/s43441-021-00271-2. Epub 2021 Mar 23. Ther Innov Regul Sci. 2021. PMID: 33755928
-
How Aggregate Safety Assessment Planning Supports Investigational New Drug Safety Reporting Decisions.Ther Innov Regul Sci. 2024 Jul;58(4):579-590. doi: 10.1007/s43441-024-00634-5. Epub 2024 Mar 30. Ther Innov Regul Sci. 2024. PMID: 38555342
-
Patient-Reported Outcome Measures in Safety Event Reporting: PROSPER Consortium guidance.Drug Saf. 2013 Dec;36(12):1129-49. doi: 10.1007/s40264-013-0113-z. Drug Saf. 2013. PMID: 24092596 Free PMC article.
-
A primer of drug safety surveillance: an industry perspective. Part III: Managing adverse-event data.J Pharm Technol. 1992 Nov-Dec;8(6):259-73. doi: 10.1177/875512259200800608. J Pharm Technol. 1992. PMID: 10122649 Review.
-
Postmarketing surveillance and other epidemiologic uses of drug prescription data in the United States.Ann Ist Super Sanita. 1991;27(2):235-7. Ann Ist Super Sanita. 1991. PMID: 1755576 Review.
References
-
- Hendrickson BA, Wang W, Ball G, Bennett D, Bhattacharyya A, Fries M, et al. Aggregate safety assessment planning for the drug development life-cycle. Ther Innov Regul Sci. 2021;55(4):717–32. https://doi.org/10.1007/s43441-021-00271-2 . - DOI - PubMed
-
- Gershon AA, Breuer J, Cohen JI, Cohrs RJ, Gershon MD, Gilden D, et al. Varicella zoster virus infection. Nat Rev Dis Primers. 2015;1:15016. https://doi.org/10.1038/nrdp.2015.16 . - DOI - PubMed - PMC
-
- Wareham DW, Breuer J. Herpes zoster. BMJ. 2007;334(7605):1211–5. https://doi.org/10.1136/bmj.39206.571042.AE . - DOI - PubMed - PMC
-
- Gondivkar S, Parikh V, Parikh R. Herpes zoster oticus: a rare clinical entity. Contemp Clin Dent. 2010;1(2):127–9. https://doi.org/10.4103/0976-237X.68588 . - DOI - PubMed - PMC
-
- Kawai K, Gebremeskel BG, Acosta CJ. Systematic review of incidence and complications of herpes zoster: towards a global perspective. BMJ Open. 2014;4(6):e004833. https://doi.org/10.1136/bmjopen-2014-004833 . - DOI - PubMed - PMC
MeSH terms
LinkOut - more resources
Full Text Sources