About this trial
Background. Pulmonary arterial hypertension (PAH) is a heterogeneous pathophysiological condition characterized by progressive pulmonary vascular narrowing that ultimately results in right-sided heart failure and eventually death or lung transplantation. The effectiveness of current pharmacological treatments is suboptimal and a large proportion of patients still had events or died despite receiving combination therapy. Vitamin D deficiency has been found to be much more frequent in PAH patients than in the general population or even compared to patients with other severe cardiovascular diseases. Moreover, vitamin D deficiency has a negative prognostic impact in PAH. Animal studies support that vitamin D deficiency worsens PAH.
Hypothesis. In patients with PAH and vitamin D deficiency, restoration of vitamin D status with calcifediol improves their symptomatology and prognosis.
Design: Multicenter clinical trial with the participation of 9 hospitals, placebo-controlled, randomized (1:1 ratio), in two parallel groups (without crossover), triple blind, and add-on on existing treatments (add-on). It will include at least 102 subjects (51 in the calcifediol group and 51 in the placebo group) followed for 24 weeks of treatment.
Inclusion criteria: Patients of both sexes (18-75 years) with hemodynamic diagnosis of PAH and severe vitamin D deficiency (25-OHvitD \<= 12 ng/ml) and without previous diagnosis of osteoporosis or osteomalacia.
Treatments: 1) Calcifediol Hydroferol® 0.266 mg once every 10 days for the first 12 weeks and once every two weeks for the following 12 weeks. 2) Placebo.
Main objective: A composite endpoint of clinical improvement without clinical worsening at week 24.
Expected outcome: Restoration of vitamin D status is an unexpensive measure, very easily implantable and that could improve the evolution of the disease as well as other aspects such as bone or immune health and that has few side effects.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Male and female patients aged 18 -75 years.
Patients with diagnosis of PAH of the following types according to 2022 ERS/ESC guidelines: idiopathic, hereditary, drug and toxin-induced PAH or associated to connective tissues disease.
Patients who are stable and treated with standard medications for PAH on monotherapy or with combinations of drugs, including calcium channel blockers, phosphodiesterase type 5 inhibitors (PDE5i), endothelin receptor antagonists (ERA), prostacyclin analogues or selexipag or with stable dose of diuretics who had no treatment modification for at least 6 weeks before randomization.
Patients with an intermediate-low and intermediate-high risk score according to 2022 ERS/ESC guidelines.
Disqualifiers
Participation in another interventional clinical study within 30 days before screening.
Previous randomisation to treatment during this study (no re-randomisation).
Pregnant women or breastfeeding women, or women with childbearing potential not using a effective contraception method throughout the study.
Patients with a medical disorder, condition, or history of such that would impair the patient's ability to participate in or complete this study, in the opinion of the investigator.
Trial design
Parallel
Treatments tested in this trial
Calcifediol Oral Capsule
DrugOne Hydroferol® soft capsule (0.266 mg) will be administered once weekly for the first 12 weeks and one capsule every two weeks for the next 12 weeks.
Placebo
DrugOne soft capsule will be administered once weekly for the first 12 weeks and one capsule every two weeks for the next 12 weeks.
Treatment groups
Trial outcomes
Primary outcomes
Clinical improvement without clinical worsening
Clinical improvement is defined as a change in at least two of the following variables: 1) increase in 6 minutes walking distance (6MWD) \>= 10% or more than 30 m, 2) change from intermediate-low or intermediate-high risk to low risk score or change from intermediate-high to intermediate-low risk according to 2022 ERS/ESC guidelines), 3) reduction in BNP or NT-proBNP \>= 30%, 4) increase in the TAPSE/SPAP ratio \>= 25%. Clinical worsening is defined as any of the following events: a) hospitalization related to PAH, b) therapeutic escalation, c) progression of symptoms, d) lung or cardiopulmonary transplantation, e) atrial septostomy and f) mortality related to PAH.
Secondary outcomes
6 minute walking distance
Difference from baseline (active vs placebo)
serum BNP or nt-pro-BNP
Difference from baseline (active vs placebo)
functional class (WHO/NYAS)
Difference from baseline (active vs placebo)
noninvasive risk score (NIRS) based on the three previous variables
Difference from baseline (active vs placebo)
Locations
Sponsors and contacts
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Parc de Salut Mar
Lead sponsor
Universidad Complutense de Madrid
Collaborator
Hospital Clinic of Barcelona
Collaborator
Hospital Vall d'Hebron
Collaborator
Hospital Universitario Marqués de Valdecilla
Collaborator
Hospital Universitario de Gran Canaria Doctor Negrín
Collaborator
Hospital Universitario La Fe
Collaborator
Hospital Universitario Doctor Peset
Collaborator
Hospital Universitario Ramon y Cajal
Collaborator
Hospitales Universitarios Virgen del Rocío
Collaborator
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