Question

Question Posted 02/03/26:
Dear Team,
We would like to confirm whether adverse event (AE) data from the ADNI registry are available for research. We are conducting a feasibility study and we observed that AE information appears abbreviated in the dataset currently accessible to us. We noted that such data have been utilized previously, for example, in the following publication by Henley DB, et al. (2012) doi:10.1016/j.jalz.2011.05.2413. This study compared safety data from AD trials with patient-level data from ADNI and reported background rates of serious adverse events, including malignancies and cerebrovascular accidents. Our objective is to adopt a similar approach to contextualize safety findings in our ongoing research. Could you kindly confirm whether these AE data are currently accessible and, if so, advise on the process for requesting access?
Thank you very much for your time and support.
Response posted 02/04/26 by Paola Nasuti:
Thank you for responding to my query. Here is your response: Thank you for using our Ask the Expert feature! Your question has been answered below.

Answer: Yes, data from both the Adverse Events Log and Adverse Events/ Hospitalizations eCRFs are available to approved ADNI investigators.
I would really appreciate if you could explain the process to follow in order to become approved ADNI investigators. Or whether we could establish a collaboration with specific ADNI investigators.
Thank you very much



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