Bumetanide in Patients with Alzheimer's Disease (BumxAD): A Phase IIa Clinical Trial

This ongoing study is funded by the Stanford Knight Initiative for Brain Resilience and IRB approved. The inclusion criteria include mild cognitive impairment or mild dementia due to AD, AD medications are planned to remain stable throughout, willingness and ability to complete all aspects of the study including assessments, neuropsychological testing, and MRI. Exclusion criteria includes clinically significant abnormalities in screening laboratory tests, chronic liver disease, renal insufficiency, poorly managed hypertension and participants taking the following concomitant medications, based on the current Prescribing Information for bumetanide: lithium, drugs with ototoxic potential, drugs with nephrotoxic potential, probenecid, and indomethacin CONCLUSION: We present the clinical trial protocol and design for a phase II trial evaluating the effect of bumetanide in AD.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2025-12-01
DOI
https://doi.org/10.1002/alz70859_106859
Primary Topic
Dementia and Cognitive Impairment Research
Type
article
Field-Weighted Citation Impact
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article

Bumetanide in Patients with Alzheimer's Disease (BumxAD): A Phase IIa Clinical Trial

François Haddad, Irina A. Skylar-Scott, Kyan Younes, Maria Coburn et al.
Alzheimer s & Dementia
Dementia and Cognitive Impairment Research
article

Bumetanide in Patients with Alzheimer's Disease (BumxAD): A Phase IIa Clinical Trial

François Haddad, Irina A. Skylar-Scott, Kyan Younes, Maria Coburn, Niyatee Samudra, Michael D. Greicius, Ted N. Wilson, Tony Wyss‐Coray, Minhtrang Chu, Mina Kmiecik, Annie Zhou, Zihuai He, Sharon J Sha, Pragya Tripathi
article en

Abstract

This ongoing study is funded by the Stanford Knight Initiative for Brain Resilience and IRB approved. The inclusion criteria include mild cognitive impairment or mild dementia due to AD, AD medications are planned to remain stable throughout, willingness and ability to complete all aspects of the study including assessments, neuropsychological testing, and MRI. Exclusion criteria includes clinically significant abnormalities in screening laboratory tests, chronic liver disease, renal insufficiency, poorly managed hypertension and participants taking the following concomitant medications, based on the current Prescribing Information for bumetanide: lithium, drugs with ototoxic potential, drugs with nephrotoxic potential, probenecid, and indomethacin CONCLUSION: We present the clinical trial protocol and design for a phase II trial evaluating the effect of bumetanide in AD.

Alzheimer s & DementiaVol. 21(S5)
Palo Alto University (US), Neurosciences Institute (US), Stanford University (US)
Openalex Percentile: Top 32%
Dementia and Cognitive Impairment Research
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