drugset / Trial / NCT06169826

Histidine Oral Supplementation as a Therapeutic Modality for Alzheimer's Disease

NCT06169826

RandomizedParallel-groupTriple-blindTreatment

Summary

Oral supplementation of histidine in patients with cognitive dysfunction should increase brain anserine, carnosine and histamine levels which will result in improved cognition via numerous proven in vivo mechanisms including increasing blood flow, neurogenesis, angiogenesis, activation of histaminergic neural pathways and autophagy of beta-amyloid protein, which is pathognomonic for Alzheimer's disease. Randomized into one of 2 arms to receive Histidine or placebo to take for up to 3 months. Baseline evaluation and followup evaluation at 3 months postop.

Timeline

Start
2025-04
Primary completion
2026-04
Completion
2026-04

Drugs

EvaluationDrugModalityDoseRoute
Comparator HISTIDINE Small molecule 8 g Oral

Indications