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Completed Phase 2 Interventional Results available

A Randomized Study to Assess the Safety of GRF6019 Infusions in Subjects With Mild to Moderate Alzheimer's Disease

ClinicalTrials.gov ID: NCT03520998

Public ClinicalTrials.gov record NCT03520998. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 10, 2026, 3:42 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official 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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT03520998
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Alkahest, Inc.
Industry
Enrollment
47 participants

Conditions and interventions

Eligibility (public fields only)

Age range
60 Years to 90 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 15, 2018
Primary completion
May 23, 2019
Completion
May 23, 2019
Last update posted
Jan 28, 2021

2018 – 2019

United States locations

U.S. sites
10
U.S. states
5
U.S. cities
10
Facility City State ZIP Site status
Synergy East Lemon Grove California 91945
CNS Network Long Beach California 90806
Pacific Research Network San Diego California 92103
MD Clinical Hallandale Florida 33009
Miami Jewish Health Systems Miami Florida 33137
Behavioral Clinical Research North Miami Florida 33161
Bioclinica Research Orlando Florida 32806
Princeton Medical Institute Princeton New Jersey 08540
Serenity Inpatient DeSoto Texas 75115
PRA Health Sciences Salt Lake City Utah 84124

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03520998, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 28, 2021 · Synced Sep 10, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03520998 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →