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Clinical Trials/NCT02772068
NCT02772068
Completed
Early Phase 1

Hemodynamic Response to Exercise in Heart Failure With Preserved Ejection Fraction (HFpEF) Patients After Upregulation of SERCA2a

Benjamin Levine1 site in 1 country26 target enrollmentSeptember 15, 2015

Overview

Phase
Early Phase 1
Intervention
Istaroxime
Conditions
Heart Failure, Congestive
Sponsor
Benjamin Levine
Enrollment
26
Locations
1
Primary Endpoint
Change in cardiac filling pressures (pulmonary capillary wedge pressure) during exercise with Istaroxime
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Heart failure with preserved ejection fraction or HFpEF, represents nearly 50% of all heart failure cases and is particularly common in the elderly. The disease has no current treatment options. Symptoms typically occur during exertion or exercise and is likely the result of increased cardiac and pulmonary congestion as a result of impaired diastolic function. Istaroxime is a novel activator of SERCA2a, an important regulator of calcium uptake within the myocyte. We will test the hypothesis that Istaroxime will improve diastolic function during exercise in HFpEF patients which in turn will reduce cardiac and pulmonary congestion.

Detailed Description

About half of all elderly patients with a diagnosis of congestive heart failure have apparently normal systolic function, so called "heart failure with a preserved ejection fraction" or HFpEF. To date, no effective therapy for HFpEF has been found, in part because of failure to discern key pathophysiologic pathways. An extensive amount of pre-clinical work has identified that altered sarcoplasmic reticulum (SR) Ca2+ uptake, storage, and release play a major role in the changes in cardiac relaxation associated with aging, especially regarding sequestration of Ca++ by the sarcoplasmic reticular Ca++-ATPase (SERCA2a), which causes cardiac muscle relaxation by reducing cytosolic Ca++. Istaroxime is a relatively new drug that augments lusitropic function by upregulating SERCA2a activity in the heart. Because of the clear importance of slowed relaxation in HFpEF, and the evidence that depressed SERCA2a activity contributes to the slowed relaxation with aging, the proposed study may be establish the "impairment of SERCA2a" hypothesis as a mechanism of impaired relaxation in HFpEF subjects.

Registry
clinicaltrials.gov
Start Date
September 15, 2015
End Date
December 1, 2018
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Benjamin Levine
Responsible Party
Sponsor Investigator
Principal Investigator

Benjamin Levine

Professor

University of Texas Southwestern Medical Center

Eligibility Criteria

Inclusion Criteria

  • age \> 60 years

Exclusion Criteria

  • Coronary Ischemia
  • No chronic medical problems
  • BMI \> 30 kg/m2
  • HFpEF Subjects
  • Inclusion Criteria:
  • age \> 60 years
  • signs and symptoms of heart failure
  • ejection fraction \> 50%
  • objective evidence of diastolic dysfunction
  • Exclusion Criteria:

Arms & Interventions

Healthy Senior Control

Fifteen healthy senior subjects will perform light exercise at a fixed heart rate of 100 beats per minute. Subjects will then be given either placebo infusion (normal saline) or Istaroxime infusion for one hour. Subjects will be blinded to which infusion they are receiving. Subjects will then repeat light exercise at a fixed heart rate of 100 beats per minute. Primary outcome is changes in cardiac filling pressures during exercise.

Intervention: Istaroxime

Healthy Senior Control

Fifteen healthy senior subjects will perform light exercise at a fixed heart rate of 100 beats per minute. Subjects will then be given either placebo infusion (normal saline) or Istaroxime infusion for one hour. Subjects will be blinded to which infusion they are receiving. Subjects will then repeat light exercise at a fixed heart rate of 100 beats per minute. Primary outcome is changes in cardiac filling pressures during exercise.

Intervention: Exercise

Heart failure patients

Fifteen HFpEF subjects will perform light exercise at a fixed heart rate of 100 beats per minute. Subjects will then be given either placebo infusion (normal saline) or Istaroxime infusion for one hour. Subjects will be blinded to which infusion they are receiving. Subjects will then repeat light exercise at a fixed heart rate of 100 beats per minute. Primary outcome is changes in cardiac filling pressures during exercise.

Intervention: Istaroxime

Heart failure patients

Fifteen HFpEF subjects will perform light exercise at a fixed heart rate of 100 beats per minute. Subjects will then be given either placebo infusion (normal saline) or Istaroxime infusion for one hour. Subjects will be blinded to which infusion they are receiving. Subjects will then repeat light exercise at a fixed heart rate of 100 beats per minute. Primary outcome is changes in cardiac filling pressures during exercise.

Intervention: Exercise

Outcomes

Primary Outcomes

Change in cardiac filling pressures (pulmonary capillary wedge pressure) during exercise with Istaroxime

Time Frame: Immediate; 90 minutes after infusion

Change in cardiac filling pressures (pulmonary capillary wedge pressure) during exercise with Istaroxime

Secondary Outcomes

  • Change in cardiac relaxation time (isovolumic relaxation time) during exercise with Istaroxime(90 minutes)

Study Sites (1)

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