Thanks to those who have already contributed to this survey on current practices in preclinical ADA testing
If you would still like to be included, the poll is still open at this link: Current Practices in Preclinical ADA Testing – Fill in form
Best wishes,
Rob
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Robert Nelson
Scientific Officer, Executive Director
BioAgilytix Laboratories
[email protected]Disclaimer: Opinions expressed are solely my own and do not express the views or opinions of my employer or other entities to which I am affiliated.
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Original Message:
Sent: 02-25-2026 13:02
From: Robert Nelson
Subject: Current Practices in Preclinical ADA Testing
Hi all,
We've recently had several discussions within the community around streamlined approaches to preclinical ADA testing in GLP toxicology studies. In parallel, we've seen evolving thinking in this space, including the strategic approach proposed by the EBF (Laurén et al., 2021. A strategic approach to nonclinical immunogenicity assessment: a recommendation from the European Bioanalysis Forum, link here).
To better understand where the field currently stands, I've put together a short (~2 minute) poll to capture current industry practice.
The survey explores:
- Tiered vs streamlined ADA workflows (1-tier, 2-tier, 3-tier)
- Trigger-based vs routine testing approaches
- Key drivers influencing strategy selection
If you're willing to contribute, the survey can be accessed here: Current Practices in Preclinical ADA Testing – Fill in form
Responses will be treated confidentially, and only aggregated trends will be shared back with the community.
I'd be very interested in capturing a broad range of sponsor and CRO perspectives.
Thanks in advance for your input,
Rob
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Robert Nelson
Scientific Officer, Executive Director
BioAgilytix Laboratories
[email protected]
Disclaimer: Opinions expressed are solely my own and do not express the views or opinions of my employer or other entities to which I am affiliated.
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