Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03852901
Other study ID # 190060
Secondary ID 19-AG-0060
Status Completed
Phase Phase 1
First received
Last updated
Start date March 28, 2019
Est. completion date December 13, 2021

Study information

Verified date December 13, 2021
Source National Institutes of Health Clinical Center (CC)
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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 it does not have enough glucose for fuel. The brains of many people with age-related diseases like Alzheimer's do not use glucose well. Brain use of ketones might improve mental ability. We investigated how empagliflozin affects ketone levels, which could lead to ways to improve brain health as people age. Objectives: To study how taking empagliflozin affects systemic and brain metabolism including ketone levels in people without diabetes. Eligibility: Adults at least 55 years old without diabetes Design: After a screening Visit, eligible participants were admitted to the NIA Clinical Unit during Visits 1 (baseline), 2 (first dose) and 3 (last/14th dose). On each Visit, blood draws were performed and circulating metabolites and hormones were repeatedly measured over 34-hour periods. Using plasma from fasting state only, we isolated total and neuronal-origin extracellular vesicles to measure proteins of the IGF-1 and insulin signaling cascades. Furthermore, on each Visit, we performed magnetic resonance spectroscopy (MRS) to measure concentrations of a plethora of metabolites in the brain. Between Visits 2 and 3, participants were taking the drug at home. A continuous glucose monitoring device was placed to detect potential glucose fluctuations while at home. The study was concluded for participants after the end of Visit 3.


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 bodies and metabolites used for gluconeogenesis. We also hypothesized that empagliflozin would increase circulating glucagon and fatty acids, decrease circulating amino acids, upregulate IGF-1 and insulin cascades in plasma extracellular vesicles, and change MRS brain metabolism measures. Experimental Design and Methods: men and women (total n=21) were recruited for this pilot study. Each eligible participant had a screen visit (Visit 0) and three additional 2-day study visits (Visit 1-3). On Visits 1, 2 and 3, frequent blood sampling for beta-hydroxybutyrate butyrate (BHB), acetoacetate (AcAc), fatty and amino acids, glucagon, insulin and glucose levels will be carried out; these visits also included blood work for extracellular vesicle biomarkers and brain MRS. In addition, placement of a continuous glucose monitor (CGM) along with a 34-hour urine collection was carried out. On Visit 2 the participants wore the CGM until they returned for their next Visit. On Visit 3 the CGM was removed at the end of the study Visit. On Visit 1, no empagliflozin was administered. Participants returned in 13 +/- 2 days for Visit 2. Visit 2 was the same as Visit 1 except empagliflozin 25 mg was administered both mornings, at least 30 minutes before eating breakfast and participants continueed empagliflozin 25 mg once every morning, at least 30 minutes before eating breakfast, at home until they returned in 13 +/- 2 days for Visit 3. At the end of Visit 3, empagliflozin was stopped. Medical Relevance and Expected Outcome: Elevating ketone bodies may bolster neuronal health and delay onset and progression of cognitive impairment. The expected outcome of this study was an increase in circulating levels of ketones, glucagon and fatty acids, an increased expression of receptors and mediators of ketone metabolism in plasma exosomes, an upregulation of IGF-1/insulin cascades in exosomes, and a change in Magnetic Resonance Spectroscopy (MRS) brain metabolism measures, in subjects taking a sGLT2 inhibitor. We expected circulating amino acid levels to decrease, especially during the overnight hours. This study will aid in deciding whether this class of compound may be used in a larger study to improve cognitive function in patients with diagnosis consistent with declining cognitive function. We required that empagliflozin was taken for up to 2 weeks before returning for Visit 3, because we needed to fully understand the homeostatic adaptations that may occur in the metabolite response to empagliflozin due to prolonged (up to 2 weeks) sGLT2 inhibition. It is our goal in the future to use the information gathered in this pilot study to design a long-term study in people who actually suffer from mild cognitive impairment/Alzheimer's disease and therefore a Visit 2 (34-hour acute study) only, as outlined above, would not give us the full picture of the metabolic changes that might occur with prolonged use, especially in a non-diabetic population.


Recruitment information / eligibility

Status Completed
Enrollment 21
Est. completion date December 13, 2021
Est. primary completion date November 12, 2020
Accepts healthy volunteers No
Gender All
Age group 55 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
empagliflozin (Jardiance) 25 mg
Oral empagliflozin 25 mg/day x 14 days

Locations

Country Name City State
United States National Institute on Aging, Clinical Research Unit Baltimore Maryland

Sponsors (1)

Lead Sponsor Collaborator
National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Serum ß-hydroxybutyrate (BHB) Change in serum ß-hydroxybutyrate (BHB) after 14 days on empagliflozin, compared with baseline. 14 days
Secondary Change in Plasma Glucose Change in plasma glucose after 14 days on empagliflozin, compared with baseline. 14 days
Secondary Change in Serum Non-esterified Fatty Acids (NEFAs) Change in serum non-esterified fatty acids (NEFAs) after 14 days on empagliflozin, compared with baseline. 14 days
Secondary Change in Plasma Insulin Change in plasma insulin after 14 days on empagliflozin, compared with baseline. 14 days
Secondary Change in Serum Acetoacetate (AcAc) Change in serum Acetoacetate (AcAc) after 14 days on empagliflozin, compared with baseline. 14 days
Secondary Change in 1H MRS BHB Change in 1H MRS ß-hydroxybutyrate (BHB) after 14 days on empagliflozin, compared with baseline. 14 days
Secondary Change in 1H MRS Glutamate (Glu) Change in 1H MRS glutamate (Glu) after 14 days on empagliflozin, compared with baseline. 14 days
Secondary Change in 1H MRS Glutamine (Gln) Change in 1H MRS glutamine (Gln) after 14 days on empagliflozin, compared with baseline. 14 days
See also
  Status Clinical Trial Phase
Completed NCT05321602 - Study to Evaluate the PK Profiles of LY03010 in Patients With Schizophrenia or Schizoaffective Disorder Phase 1
Active, not recruiting NCT05284097 - Ad26.ZEBOV, MVA-BN-Filo Vaccination in Children and Adults Previously Vaccinated With Control in the EBOVAC-Salone Study Phase 2
Recruiting NCT05794503 - Postoperative Urinary Retention After Reversal of Neuromuscular Block by Neostigmine Versus Sugammadex Early Phase 1
Completed NCT03294473 - Centralized Reminder Recall - Flu RCT2 N/A
Withdrawn NCT03989635 - Mechanistic Study of Anti-inflammatory Effects of Fevipiprant in Patients With Eosinophilic Asthma. Phase 2
Terminated NCT04489420 - Natural Killer Cell (CYNK-001) IV Infusion or IT Administration in Adults With Recurrent GBM Phase 1
Completed NCT03841292 - Using Non-invasive Brain Stimulation (tDCS) With Varenicline for Treating Tobacco Dependence N/A
Suspended NCT03722186 - Safety, Tolerability and Pharmacokinetics/Pharmacodynamics (PK/PD) of SHR-1603 in Subjects With Advanced Malignancies Phase 1
Recruiting NCT04045301 - Omalizumab to Accelerate a Symptom-driven Multi-food OIT Phase 2
Completed NCT03838120 - Determination of Minimum Effective Volume of Local Anesthetic in Patients Undergoing Ultrasound-Guided Infraclavicular Approach for Brachial Plexus Blockade Phase 4
Completed NCT03964350 - Behavior Brain Responses Early Phase 1
Recruiting NCT03655847 - Acceptable Hemodynamic Changes in Dexmedetomidine for Single Intravenous Bolus Injection Phase 4
Active, not recruiting NCT04365101 - Natural Killer Cell (CYNK-001) Infusions in Adults With COVID-19 Phase 1/Phase 2
Active, not recruiting NCT04309084 - Natural Killer Cell (CYNK-001) Infusions in Adults With Multiple Myeloma Phase 1
Completed NCT03677336 - Oral Dydrogesterone (OD) Versus Micronized Vaginal Progesterone (MVP) for Luteal Phase Support (LPS) in IVF/ICSI Phase 4
Recruiting NCT04729478 - Comparison Between Natural Sleep Endoscopy and Drug-induced Sleep Endoscopy in Patients With Obstructive Sleep Apnea N/A
Completed NCT00280774 - Memantine for Corticosteroid-Induced Mood and Declarative Memory Changes Phase 4
Recruiting NCT04310592 - Natural Killer Cell (CYNK-001) Infusions in Adults With AML Phase 1
Completed NCT03718286 - Effects of Acute, Rapid Lowering of LDL Cholesterol With Alirocumab in Patients With STEMI Undergoing Primary PCI Phase 2
Not yet recruiting NCT06462196 - Natural History of Depression, Bipolar Disorder and Suicide Risk