Could a diabetes drug help detect Alzheimer's early?
NCT ID NCT03560960
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This early-phase study tests whether a single injection of pramlintide, a diabetes drug, can temporarily increase levels of Alzheimer's-related proteins in the blood, potentially revealing early signs of the disease. Researchers will measure changes in beta-amyloid and tau proteins before and after injection in 57 people with mild cognitive impairment, Alzheimer's, or normal cognition. The goal is to develop a simple, accessible blood test for early Alzheimer's detection.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Pramlintide (Symlin)
- What this could lead to
- If successful, this could lead to a simple blood test for early Alzheimer's detection, helping diagnose the disease before severe symptoms appear.
- What could go wrong
- This is a very early, small study (57 people) testing a biomarker, not a treatment. The approach may not reliably distinguish early Alzheimer's from other conditions.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
-
57 people
The number who actually took part.
- Started
-
Feb 2020
- Expected to finish
-
Nov 2026
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
60 to 90 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Current research subjects at the BU , Memory Center VA Boston Healthcare, or Indiana University Alzheimer Disease Center * A consensus diagnosis of probable Alzheimer's Disease (AD), amnestic mild cognitive impairment (MCI), or control * BMI of 20-35 * Probable AD subjects must be confirmed for positive AD pathology in the central nervous center (CNS0 * Probable AD subjects must have a designated research proxy signed before they became demented. Exclusion Criteria: * Diabetes mellitus * Gastroparesis * Use of insulin, pramlintide, other injectable anti-hyperglycemic agents, such as glucagon like peptide-1 (GLP-1), or oral anti-diabetic products * Unexplained hypoglycemia (glucose ≤ 60 mg/dL) or hyperglycemia (glucose ≥ 126 mg/dL) pre-injection * History of stroke * Seizures or use of anti-seizure medications * History of brain injury and loss of consciousness * Diagnosed cerebral amyloid angiopathy (CAA) * Infection within 1 month
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
BU Alzheimer Disease Center
Boston, Massachusetts, 02118, United States
-
Indiana University Alzheimer Disease Center
Indianapolis, Indiana, 46202, United States
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Memory Center VA Boston Healthcare
Jamaica Plain, Massachusetts, 02130, United States
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