Status:

COMPLETED

Sodium-glucose Co Transporter 2 (sGLT2) Inhibitor and Endogenous Ketone Production

Lead Sponsor:

National Institute on Aging (NIA)

Conditions:

Empaglifozin

Physiological Effects of Drugs

Eligibility:

All Genders

55+ years

Phase:

PHASE1

Brief Summary

Background: The drug empagliflozin treats diabetes. It lowers blood sugar by increasing glucose the kidneys excrete. This increases levels of ketones formed in the blood. The body makes ketones when ...

Detailed Description

Objective and Specific Aims: The objective of this proof-of-concept study was to demonstrate in non-diabetic men and women age \> 55 years that a sGLT2 inhibitor (empagliflozin) can increase ketone bo...

Eligibility Criteria

Inclusion

  • INCLUSION CRITERIA:
  • Age 55 years and older.
  • Healthy (see exclusion criteria below).
  • Able to understand the study risks and procedures, and consent to participate in the study.
  • Able to read and speak English.
  • EXCLUSION CRITERIA:
  • History of diabetes (requiring any medical treatment other than diet and exercise) or fasting plasma glucose \> 126 mg/dl or HbA1c\> 6.5 %.
  • History of hypoglycemia.
  • BMI \> 35 kg/m(2).
  • Creatinine clearance less than 60 ml/min as measured by GFR.
  • Glucosuria
  • History of anemia within the past 6 months or Hgb \<11.0 mg/dL for women and Hgb \<12.5 mg/dL for men.
  • Current steroid use or steroid use within 90 days of screening, excluding eye drops.
  • Currently taking loop diuretics (Lasix, for example).
  • Participant presently following a calorie restriction diet, low carb/high fat diet.
  • HIV virus infection
  • Hepatitis B infection, as evidenced by a positive HBsAG at screen visit.
  • Hepatitis C infection that has not been treated. (The screen blood work must show HCV RNA quantitative is not detectable).
  • Active infection/fever that may cause changes in glucose metabolism.
  • Known allergy to sGLT2 inhibitors in the past.
  • Thyroid dysfunction that is not controlled or treated. This will be determined by Free T3, T4, Free T4 or TSH not within MedStar Harbor Hospital laboratory normal ranges for this pilot study.
  • Adrenal dysfunction as determined by a cortisol level not within the normal range for MedStar Harbor Hospital Laboratory for this pilot study.
  • Kidney or liver disease, (GFR \< 60 mL/min/1.73 m(2) and/or liver enzymes not within normal ranges for MedStar Harbor Hospital Laboratory for this pilot study.
  • Severe gastrointestinal diseases such as Crohn s disease or ulcerative colitis requiring continuous treatment.
  • History of severe pulmonary disease such as chronic obstructive pulmonary disease (COPD) or asthma requiring continuous medication use.
  • Patients with known, or evidence of, peripheral vascular disease.
  • History of chronic urinary tract infections.
  • History of recurrent or recent dehydration in the past year.
  • History of recurrent or recent vaginal yeast infection.
  • Alcohol intake greater than 30 grams (drink more than 2 beers OR equivalent per day).
  • History of severe psychiatric conditions associated with behavioral problems or requiring chronic medical treatment.
  • Poor venous access.
  • Inability to walk 2,000 steps
  • Donation or loss of 400 mL or more of blood within 56 days prior to and subsequent to screening.
  • Participation in another study in the past 30 days, in which a study drug was administered.
  • Currently participating in another study unless the investigator feels it would not interfere with the study.
  • History of a medical condition or any other reason that, in the opinion of the investigator, will make participation in this study unsafe.
  • Blood work or urine tests that are not considered by the study physician to be in an acceptable range for the study.
  • Metal implants and devices incompatible with 3T Magnetic Resonance Imaging (MRI), or another contraindication to MRI.

Exclusion

    Key Trial Info

    Start Date :

    March 28 2019

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    December 13 2021

    Estimated Enrollment :

    21 Patients enrolled

    Trial Details

    Trial ID

    NCT03852901

    Start Date

    March 28 2019

    End Date

    December 13 2021

    Last Update

    August 2 2022

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    National Institute on Aging, Clinical Research Unit

    Baltimore, Maryland, United States, 21224