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CompletedNCT03887741Updated Dec 31, 2024

Plasmapheresis Versus Plasma Infusion from Young APOE3 Homozygotes Into MCI APOE4 Homozygotes to Slow Disease Progression

A Phase 1 interventional study of Plasmapheresis and Plasma infusion in Mild Cognitive Impairment, sponsored by Mayo Clinic. Completed at 1 site in United States. Open to participants aged 50 Years to 75 Years. Per ClinicalTrials.gov, last updated 2024-12-31.

Sponsored by Mayo Clinic · Phase 1, Interventional, and Treatment

From the registry’s dates

  • Primary completion was Feb 2024, 2 years 7 months ago, and no results have been posted to the registry.
Phase
Phase 1
Study type
Interventional
Enrollment
3
Allocation
Non-randomized
Ages
50 Years to 75 Years
Sex
All
01

Study summary

Determine safety of plasma infusion or exchange in APOE 44 patients.

02

Conditions studied

  • Mild Cognitive Impairment
03

In context

Disease Progression

544 studies on the registry are indexed under Disease Progression; 144 are open to participants now.

This study's enrollment of 3 is below the median of 87 across 266 interventional studies indexed under Disease Progression.

Browse Disease Progression studies →

Lead sponsor

Mayo Clinic is the lead sponsor of 3,218 studies on the registry; 670 are open to participants now.

Of its 445 completed or terminated interventional studies of FDA-regulated products, 313 (70%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
50 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patient age 50 to 75.
  • APOE 44 homozygote.
  • Meets the Petersen criteria for MCI (41).
  • Clinical Dementia Rating (CDR) of 0.5 and Mini Mental Status Examination (MMSE) of 24 to 30 inclusive.
  • Has an informant who the investigator judges has sufficient patient contact to provide accurate information.
  • Stable depression and or anxiety.
  • Stable psychoactive medication for 6 weeks.

Exclusion criteria

Exclusion criteria

  • History of severe reaction to plasma or plasma derived products which include but not limited to severe allergic reaction, anaphylactic reaction and transfusion related acute lung injury (TRALI).
  • Patients who do not want to receive blood transfusion for religious or cultural reasons such as Jehovah Witness Faith.
  • Has a medical condition that would interfere with participation such as congestive heart failure (New York Heart Association Class III or IV), unstable angina, moderate to severe renal impairment, liver failure, and poorly controlled diabetes.
  • History of autoimmune disease considered clinically significant or requiring chronic steroid or immune suppression medication.
  • History of being HIV +.
  • History of +VE test result indicating active hepatitis C or B (defined as both hepatitis B surface antigen and hepatitis core antibody +VE).
  • Uncontrolled hypertension as defined by systolic/diastolic BP three times more than 165/100.
  • No venous access for plasma exchange therapy.
  • Any neurological condition that could be contributing to cognitive decline such as Lewy body disease, front temporal dementia, strokes or other cerebrovascular disease, head trauma, substance abuse, multiple sclerosis, Vitamin B12 deficiency, thyroid deficiency.
  • Epileptic seizures within 10 years of screening.
  • Cancer diagnosis (other than non-melanoma skin cancer) in the last 5 years.
  • More than 1 subcortical stroke or more than 1 cortical stroke.
  • Unable to have an MRI.
  • MRI showing acute or subacute hemorrhage, evidence of normal pressure hydrocephalus, hemispheric infarcts, glioma or other brain tumor that could contribute to cognitive decline.
  • Unstable psychiatric condition.
  • On another experimental treatment study or has been on one in the last 3 months.
  • If a patient consents to lumbar puncture (LP), they will be excluded from LP if any contraindication to having an LP is present. Examples are platelet count\<100,000, spine deformity or contraindication to come off blood thinner for the LP. Patients may still participate in the rest of the study without having and LP.
  • Any unspecified reason that the investigator finds the patient unsuitable to take part.
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
3 participants (actual)

Study arms

  • Experimental
    Plasmapheresis

    3 patients will have monthly plasmapheresis for 6 months and followed for a total of 12 months

    Biological: Plasmapheresis

  • Experimental
    Plasma infusion

    3 patients will have biweekly plasma infusion for 6 months and followed for 12 months

    Biological: Plasma infusion

  • No intervention
    Control group

    3 patients will be followed for 12 months

Interventions

  • BiologicalPlasmapheresis

    Patient will have monthly plasma exchange with young ApoE 33 plasma. Each exchange will be 1.5 volume of patient's plasma

  • BiologicalPlasma infusion

    Infuse every two weeks with ApoE33 young plasma (1unit) for 6 months

06

What researchers measure

Primary outcomes

  1. Adverse events

    Number of adverse events reported

    Time frame: One year

07

Study locations

1 site
  • Mayo Clinic in Florida
    Jacksonville, Florida 32224, United States
08

References and documents

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 31, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03887741
Lead sponsor
Mayo Clinic
Responsible party
Neill R. Graff-Radford, M.D. (Principal Investigator, Mayo Clinic) — Principal investigator
First posted
Mar 25, 2019
Start date
Sep 15, 2021
Primary completion
Feb 16, 2024
Completion
Feb 16, 2024
Last update
Dec 31, 2024

Study contacts

Neill R Graff-Radford
principal investigator · Mayo Clinic

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2024. You cannot join it, but the record below documents what was studied.

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