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Impact of Metformin on Immunity

The University of Texas System (UT) logo

The University of Texas System (UT)

Status and phase

Completed
Phase 1

Conditions

Aging
Vaccine Response Impaired

Treatments

Drug: Metformin
Drug: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT03713801
20180171H

Details and patient eligibility

About

To determine whether metformin (MET) can improve the immune response to the pneumococcal conjugate vaccine (PCV-13) in older adults.

Full description

The objective of this study is to determine whether metformin (MET) can improve the immune response to the pneumococcal conjugate vaccine (PCV-13) in older adults, and if this effect is mediated by the gut microbiota.

The proposed research projects will provide the necessary pilot data for future, more definitive, studies that will evaluate the impact of immunomodulatory therapies, such as MET therapy, on the aging immune system. The specific aims are:

Aim 1. Compare PCV13 vaccine response in elderly adults (≥63 years of age) treated with MET vs. placebo. For this study, 50 elderly volunteers will be enrolled and randomly assigned to receive MET or placebo. The hypothesis that MET can improve vaccine responsiveness by measuring serotype-specific IgG concentrations before and 30 days after PCV13 administration will be tested.

Aim 2. Determine whether the frequencies of immunophenotypes differ between elderly adults treated with MET vs. placebo. The mechanisms of MET's effect on the immune system by comparing immunophenotypes of MET and placebo groups between baseline and prior to PCV13 and between baseline and 30 days after PCV13 administration will be explored.

Enrollment

18 patients

Sex

All

Ages

63 to 90 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Age 63 to 89 years of age
  2. No history of pneumococcal vaccinations
  3. Able to take oral medications
  4. Able to provide informed consent
  5. Not currently taking metformin

Exclusion criteria

  1. Previous vaccination with any pneumococcal vaccine
  2. Metformin within the last 6 months
  3. Contraindication for PCV13
  4. History of severe adverse reaction associated with any vaccine component
  5. Residence in long-term care facility
  6. Diagnosis of diabetes (diagnosis of pre-diabetes okay)
  7. Chronic renal disease (or eGFR <50 mL/min) or renal failure (defined as receipt of renal dialysis or transplant) or nephrotic syndrome
  8. History of adverse reaction or contraindications associated with metformin
  9. Recent history or plan for radiocontrast
  10. Self-reported dementia or severe cognitive impairment
  11. Receipt of blood products within 6 months before enrollment
  12. History of heart disease (New York Heart Classification greater than class II; more than non-specific ST-T wave changes on the ECG)
  13. History of chronic obstructive pulmonary disease
  14. Poorly controlled blood pressure (systolic BP>160, diastolic BP>90 mmHg)
  15. History of an immunodeficiency
  16. Use of use of investigational products, antibiotics, probiotics, or systemic immunosuppressive therapy (systemic steroids) within 1 month of study start; patients who are taking these medications chronically, with no expected discontinuation during the study period would not be considered ineligible.
  17. Treatment with anticoagulants (warfarin)
  18. Donated blood within the last 2 months
  19. Subject is considered unsuitable for the study in the opinion of the investigator for any other reason

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

18 participants in 2 patient groups, including a placebo group

Metformin
Experimental group
Description:
Dosage is increased over the first 3 weeks up to three 500 mg tablets a day at 3 weeks, then continued on 3 tablets daily for a further 9 weeks.
Treatment:
Drug: Metformin
Placebo
Placebo Comparator group
Description:
Placebo tablet dosage is increased over the first 3 weeks up to three tablets a day at 3 weeks, then continued on 3 tablets daily for a further 9 weeks.
Treatment:
Drug: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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