Heart Failure With Preserved Ejection Fraction, Iron-deficiency
Conditions
Keywords
Heart Failure with Preserved Ejection Fraction, Iron Deficiency
Brief summary
The primary objective of this study is to determine if the correction of functional iron deficiency by administering a single dose of intravenous iron (ferric derimaltose or Monoferric®) in participants with heart failure with preserved ejection fraction (HFpEF) will improve exercise capacity as measured by the change in peak oxygen uptake (peak VO2) from baseline to 12 weeks.
Detailed description
A double-blind, prospective, randomized, placebo-controlled study to assess change in exercise capacity after iron repletion with a single dose of ferric derisomaltose (Monoferric®) IV compared to placebo in heart failure with preserved ejection fraction and with functional iron deficiency. Sixty-six HFpEF participants who have functional iron deficiency will be recruited. After undergoing other baseline measurements including cardiopulmonary exercise testing (CPET), echocardiogram, 6-minute walk tests, research biomarkers, and the Kansas City Cardiomyopathy Questionnaire (KCCQ) participants will be randomized (2:1) to either a single dose of ferric derisomaltose (Monoferric®)1000 mg/100 ml (n=44) or placebo (n=22). Given that the iron drug formulation is of brown color and the placebo is clear, unblinded staff members will be assigned to order, pick up and administer drug to the subject. The subject is blinded; therefore, the drug will be infused using a tented covering over the arm in which the IV has been placed. The tented covering will allow adequate viewing of the IV site, but outside of the view of the subject. All blinded staff will not be present during study drug infusion. Prior to infusion the subject will undergo vital signs; blood pressure, heart rate, and temperature. A peripheral intravenous catheter will be placed followed by an infusion of Monoferric 1000 mg (for subjects less than 50 kg, 20 mg/kg) as per current FDA-approved dosing or placebo over 20 minutes. Vital signs will be performed immediately after dosing and after 30 minutes. Subjects will remain in the clinic for observation for 30 minutes following infusion. Randomization will be stratified by sex and will be performed in permutated blocks of 4 to assure balanced group sizes. In order to allocate without bias, and in a manner blinded to both participants and investigators, we will use random number generation at the time of randomization. Participants will return for a CPET, echocardiogram, 6-minute walk test, KCCQ, ECG, complete metabolic panel, and blood draw for research biomarkers, cardiovascular exam, and assessment of adverse experiences.
Interventions
DRUGFerric Derisomaltose 1000 Mg in 100 mL INTRAVENOUS SOLUTION [Monoferric]
Ferric derisomaltose (Monoferric) 1000 mg X1 (for subject \<50 kg, 20 mg/kg
DRUGPlacebo
Normal saline
Sponsors
Massachusetts General Hospital
National Heart, Lung, and Blood Institute (NHLBI)
Pharmacosmos A/S
National Institutes of Health (NIH)
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Masking description
Unblinded staff (clinical research nurse and unblinded investigator) prepare and administer study drug to subject and document and follow safety events. The subject is blinded. A tented covering will allow adequate viewing of the IV site, but outside of the view of the subject. All blinded staff will not be present during study drug infusion.
Intervention model description
This is a double-blind, prospective, randomized, placebo-controlled study to assess exercise tolerance after iron repletion with a single dose of ferric derisomaltose (Monoferric®) IV compared to placebo in heart failure with preserved ejection fraction and with iron deficiency. Randomization will be stratified by sex and will be performed in permutated blocks of 4 to assure balanced group sizes
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Adult (≥18 years of age) able to provide informed consent. 2. Stable heart failure (NYHA II-IV) for at least 4 weeks 3. Heart Failure with Preserved left ventricular ejection fraction.(Left ventricular ejection fraction ≥ 50 % obtained within 6 months of informed consent. 4. NT-proBNP ≥ 125 pg/mL without ongoing atrial fibrillation/flutter. If ongoing atrial fibrillation/flutter at the time of sample collection, NT-proBNP must be ≥ 250 pg/mL OR patients must have a history of pulmonary capillary wedge pressure ≥ 15 mm Hg during rest or the slope of pulmonary capillary wedge pressure to cardiac output (PCWP/CO) ≥ 2.0 mmHg/L/min during upright exercise (Eisman et al., Circ Heart Fail. 2018 May;11(5):e004750.).OR subjects must have a heart failure hospitalization within the last 12 months prior to screening OR Chronic diastolic dysfunction on echocardiography as evidenced by: Left Atrial Enlargement (LAE): LA diameter ≥ 3.8cm in women, ≥ 4.0 cm in men or LA length ≥ 5.0 cm or LA area ≥ 20 cm2 OR LA volume ≥ 55mL or LA volume index ≥ 29ml/m2 or Left Ventricular Hypertrophy (LVH): septal thickness or posterior wall thickness ≥ 1.1 cm OR For patients in sinus rhythm: E/e' ratio ≥15 at septal annulus, or E/e' ratio ³13 at lateral annulus, or average E/e' ratio ³14. For patients in atrial fibrillation: E/e' ≥ 11 at the septal annulus. 5. Hemoglobin \>9.0 g/dL AND \<15.0 g/dL . 6. Serum ferritin \<100 ng/mL OR 100 to 300 ng/mL with TSAT \<20%, but NOT ferritin \< 15 ng/mL. 7. Demonstrate diminished exercise capacity: ≤ 75 % predicted peak VO2 as determined by a Cardiopulmonary Exercise Test (CPET) at the time of screening 8. Perform a maximal effort CPET by achieving a Respiratory Exchange Ratio (RER) of ≥ 1.05
Exclusion criteria
1. Current or planned intravenous iron supplementation. Iron-containing multivitamins (\<30 mgs /day) are permitted. 2. Known hypersensitivity reaction to any component of ferric derisomaltose (Monofer®) 3. History of acquired iron overload (e.g. hemochromatosis), or the recent receipt (within 3 months) of erythropoietin stimulating agent, IV iron therapy, or blood transfusion. 4. Documented active gastrointestinal bleeding 5. Anemia with known cause other than iron deficiency or chronic disease 6. Acute myocardial infarction, acute coronary syndrome, transient ischemic attack, or stroke within 3 months of enrollment. 7 Presence of any condition that precludes exercise testing such as: a. Claudication that limits exertion b. Uncontrolled bradyarrhythmia or tachyarrhythmia (according to Investigator judgment, pacemaker treatment is allowed as long as the same pacing mode/activity can be used at baseline and follow-up CPET) c. Clinically significant musculoskeletal disease or orthopedic conditions that limit the ability to perform the CPET (e.g., arthritis or injury in the foot, leg, knee or hip) d. Severe obesity (BMI \> 50.0 kg/m2) e. Any other non-heart failure condition that, in the opinion of the Investigator, that is the primary limitation to exercise. 8. Severe renal dysfunction (eGFR\< 20 ml/min/1.73m2) 9. Severe liver disease (ALT or AST \> 3x upper limit of normal, alkaline phosphatase or bilirubin \>2x upper limit of normal) 10. Active malignancy other than non-melanoma skin cancers 11. Female participant of child-bearing potential who is pregnant, lactating, or not willing to use adequate contraceptive precautions during the study and for up to 5 days after the last scheduled dose of study medication. 12\. Planned surgical procedure during the trial period 13. Inability to return for follow up visits
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The primary endpoint is the change in peak oxygen uptake (pVO₂, mL/kg/min) from baseline to Week 12 following a single dose of 1000mg of ferric derisomaltose or placebo. | Baseline to Week 12 | Peak VO2 measured by a maximal effort Cardiopulmonary Exercise Test (CPET) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Functional Capacity and Quality of Life Endpoint: New York Heart Association Classification (NYHA) | Baseline to Week 12 | Change in the proportion of participants with improvement of at least one New York Heart Association functional class 1 through 4. A lower score indicates a better outcome. |
| Target Engagement Endpoints: Transferrin Saturation | Baseline to Week 12 | Change in transferrin saturation measured in percent |
| Target Engagement Endpoints: Iron | Baseline to Week 12 | Change in Iron blood level measured in ug/dl |
| Target Engagement Endpoints: Ferritin | Baseline to Week 12 | Change in Ferritin measured in ug/L |
| Objectively Measured Functional Status Endpoint : Six-minute Walk Test | Baseline to Week 12 | Change in six-minute walk test measured by distance walked in meters |
| Functional Capacity and Quality of Life Endpoint : Kansas City Cardiomyopathy Questionnaire | Baseline to Week 12 | Change in Quality of Life as measured by the Kansas City Cardiomyopathy Questionnaire Overall Summary Score (KCCQ-OSS). Score range is 0-100 scale, where higher scores reflect better health status. |
| Objectively Measured Functional Status Endpoint : Oxygen uptake at the ventilatory anaerobic threshold | Baseline to Week 12 | Change in oxygen uptake at the ventilatory anaerobic threshold (VO₂ at VAT) |
Countries
United States
Contacts
PRINCIPAL_INVESTIGATORGreg Lewis, MD
Massachusetts General Hospital
Outcome results
None listed