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A Prospective, Randomized, Double-Blind, Dose-Comparison Concurrent Control Study to Assess the Safety and Tolerability of GRF6019 Infusions in Subjects With Mild to Moderate Alzheimer's Disease

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Alkahest, Inc. · 2018

Dysbiosis Human Randomized controlled trial

Abstract

This study is evaluating the safety, tolerability, and feasibility of GRF6019, a plasma-derived product, administered as an intravenous (IV) infusion, to subjects with mild to moderate Alzheimer's disease.

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Source: ClinicalTrials.gov
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Fetched: 2026-10-26 MST

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APA

Anonymous. (2018). A Prospective, Randomized, Double-Blind, Dose-Comparison Concurrent Control Study to Assess the Safety and Tolerability of GRF6019 Infusions in Subjects With Mild to Moderate Alzheimer's Disease. <em>Alkahest, Inc.</em>. https://clinicaltrials.gov/study/NCT03520998

Vancouver

Anonymous. A Prospective, Randomized, Double-Blind, Dose-Comparison Concurrent Control Study to Assess the Safety and Tolerability of GRF6019 Infusions in Subjects With Mild to Moderate Alzheimer's Disease. Alkahest, Inc.. 2018.

BibTeX

@misc{anon2018AProsp, title = {A Prospective, Randomized, Double-Blind, Dose-Comparison Concurrent Control Study to Assess the Safety and Tolerability of GRF6019 Infusions in Subjects With Mild to Moderate Alzheimer's Disease}, author = {Anonymous}, journal = {Alkahest, Inc.}, year = {2018}, }