Mangafodipir - an Intracellular Contrast Agent for Magnetic Resonance Imaging (MRI): Measuring Manganese Uptake Rate in Heart Failure Patients With Preserved Ejection Fraction (HFpEF) Patients.

The trial is an open-label, single centre, Phase 2A, Proof-of-Concept (PoC) trial in adult male and female patients without randomisation.

Overall, up to 42 participants will be enrolled in this trial:

• A run-in phase will include up to 6 participants (healthy volunteers and HFpEF patients regardless of aetiology (HCM, CA).
• The main phase of the trial will include 12 HFpEF with HCM, 12 HFpEF with CA and 12 healthy volunteers.

During a run-in phase up to 6 participants will be enrolled to standardise the trial procedures, especially mangafodipir-enhanced imaging.

The number and sequence of trial visits will be the same for participants of the run-in and the main phase.

All enrolled participants will undergo gadolinium-enhanced imaging at Visit 2. A gadolinium-based contrast agent (authorised AMP) will be injected i.v. and T1 mapping and Extracellular Volume (ECV) measurement will be done for approximately 60 minutes.

Mangafodipir-enhanced mapping will be done at Visit 3. After baseline T2 mapping, mangafodipir trisodium injection (IMP) will be administered i.v. and T1 mapping, Saturation Recovery T1 weighted imaging for measurement of the uptake rate, and T2 mapping, will be done for approximately 90 minutes.

Clinical safety data will be collected throughout the trial; the participants will be followed up by a phone call 24+6 hours after Visit 3 for evaluation of late-appearing AEs.

The analyses of the images will be done by an investigator of the study team, blinded to the clinical data.

Inclusion criteria

• Participants who have given their signed declaration of consent and data protection declaration.
• Males and females (postmenopausal or surgically sterile females) aged ≥ 18 years and ≤ 90 years
• HFpEF (= LVEF > 50%) with NYHA (New York Heart Association) class I, II and III and objective evidence of cardial structural and/or functional abnormalities consistent with the presence of left ventricular (LV) diastolic dysfunction/raised LV filling pressures, including raised natriuretic peptides.
• Patients with HCM or CA (according to current guidelines)
• Kidney functions eGFR (Estimated Glomerular Filtration Rate) > 30 mL/min/1.73 m2
• Healthy volunteers (cohort specific criteria): adults with no known pre-existing medical conditions.

Exclusion criteria

• Tachycardia (heart rate > 100, R-R interval < 600 ms)
• NYHA IV
• Previous coronary artery disease requiring intervention, including history of myocardial infarction including septal reduction therapies
• Severely reduced renal function, defined as eGFR < 30 mL/min/1.73 m2
• Severely reduced liver function (Child-Pugh class C), especially severe obstructive hepatobiliary disease
• Phaeochromocytoma
• Advanced cancer (with short/medium term prognosis)
• History of chest radiation therapy
• Diabetic patients
• Severe valvular disease
• Previous heart surgery
• Left ventricular assist device (LVAD)
• Severe pulmonary disease
• Hypersensitivity to any medicinal products containing gadolinium
• Hypersensitivity to the active substance of the IMP or to any of the excipients
• Contraindications to MRI, including implanted cardiac devices/pacemakers
• Participants not able to follow instructions necessary to conduct the MRI
• Women of childbearing potential
• Participation in other clinical studies with investigational drugs either concurrently or within the last 30 days
• Previous participation in this clinical trial
• History of ongoing drug abuse or alcoholism
• Legal incapacity and/or other circumstances rendering the patient unable to understand the nature, scope, and possible impact of the trial
• Investigator site staff and sponsor directly involved in the conduct of the study and their family members.