The Impact of IV Iron on Exercise Capacity and Quality of Life in Pulmonary Hypertension (IRON-PH)

East Limburg Hospital

Status and phase

Enrolling

Phase 4

Conditions

Iron Deficiency

Pulmonary Hypertension

Treatments

Drug: Ferric Carboxymaltose (FCM)

Drug: Sodium Chloride (NaCl) 0.9 %

Study type

Interventional

Funder types

Other

Identifiers

NCT07359599

2025-522936-14-00 (EU Trial (CTIS) Number)

Z-2025090

Details and patient eligibility

About

Pulmonary hypertension (PH) is a condition characterized by elevated blood pressure in the pulmonary arteries. This leads to symptoms such as shortness of breath and a significantly reduced exercise capacity, resulting in a very poor quality of life. Currently, treatment options for PH are limited.

More than 60% of patients with PH develop iron deficiency. Studies have shown that this deficiency is associated with more severe symptoms, reduced exercise capacity, and even lower quality of life. Oral iron supplements are often ineffective in these patients due to impaired absorption in the intestines, caused by chronic low-grade inflammation-a common feature in PH.

Intravenous iron administration can rapidly correct the deficiency, but it remains unclear whether this also leads to clinical improvements such as enhanced exercise capacity, reduced shortness of breath, and improved quality of life. Moreover, the cost-effectiveness of this treatment is still unknown. The IRON-PH study aims to answer these questions.

As part of the IRON-PH study, 306 patients with pulmonary hypertension will be enrolled. Each patient will be randomized to receive either intravenous iron (ferric carboxymaltose) or intravenous placebo (NaCl 0.9%).

Enrollment

306 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

≥18 years of age
WHO functional class II - IV
Iron deficiency defined as TSAT <21% (no more than ≥3 months old at randomization)
PH defined by echocardiography and/or right heart catheterization (RHC) according to the following WHO groups:
- Group 1 PH:
  - Patients with a diagnosis of idiopathic PAH, hereditary PAH, drug induced PAH or PAH and associated with CTD or CHD (historical RHC available) on stable and optimized doses of PAH targeted therapies for at least 4 weeks before randomization.
  - Echocardiographic evidence of a high or intermediate probability for PH as per 2022 ESC PH guidelines.
- Group 2 PH and baseline LVEF > 50% on imaging modality within last 6 months before randomization and on stable doses of loop diuretics and HFpEF therapies for 4 weeks. Group 2 PH can be included based on echocardiography or RHC.:
  - Echocardiography (<6mo before randomization):
    - Presence of LVH or LA-enlargement
    - E/e' >15 (at rest or exercise)
    - TRVmax >2.8 m/s (at rest) or mPAP/CO>3 mHg/L/min (exercise) or echocardiographic evidence of high or intermediate probability for PH as per 2022 ESC PH guidelines.
  - RHC (<6mo before randomization)
    - mPAP > 20 mmHg
    - PCWP > 15 mmHg at rest or PCWP/CO-slope > 2mmHg/L/min or exercise PCWP>25mmHg, or PCWP 13-15 mmHg with elevation ≥18mmHg after 500 cc Fluid Challenge
- Group 4 PH:
  - Inoperable CTEPH
  - Persistent/recurrent CTEPH (> 1 year after endarterectomy or > 6 months after balloon pulmonary angioplasty) ineligible for balloon pulmonary angioplasty.
  - Echocardiographic evidence of a high or intermediate probability for PH as per 2022 ESC PH guidelines.

Exclusion criteria

Screening haemoglobin < 8 g/dl or >15 g/dl
Ferritin > 700 ng/mL
Known hypersensitivity reaction to any component of FCM
Group 1 PH associated with veno-occlusive diseases.
Primary diagnosis of group 3 PH
Primary diagnosis of group 5 PH
Treatment with oral or other IV iron therapies at screening.
Current or planned mechanical circulatory support or lung/heart transplantation.
Any planned surgery or procedure leading to expected significant blood loss (defined as more than 250 ml = equal to 125mg of iron).
Haemodialysis or peritoneal dialysis (current or planned within the next 24 weeks).
Inability to return for follow up visits within the necessary windows
Concurrently in a study with another investigational product.
Uncorrected moderate to severe aortic stenosis (AVA <1.5cm² and mean gradient >20 mmHg) or severe valvular regurgitation (except tricuspid regurgitation)
Impression by investigator that patient cannot perform a 6MWT
Active infection as judged by the investigator.
Pregnancy or desire to become pregnant during the study duration.