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. 2016 Dec;25(142):381–389. doi: 10.1183/16000617.0084-2016

TABLE 1.

Potential pulmonary arterial hypertension (PAH) therapies currently in development

Therapy Clinical trial identifier Clinical trial design Primary end-points Treatment duration Status (October 2016)
Therapies targeting inflammation and immunity
 Ubenimex NCT02664558 Phase II, multicentre, randomised, double-blind, placebo-controlled trial in PAH patients Change in PVR 24 weeks Recruiting [17]
NCT02736149 Phase II, open-label, multicentre, extension study in PAH patients Frequency of adverse events ∼1 year Not yet recruiting [18]
 Rituximab NCT01086540 Phase II, randomised, double-blind, placebo-controlled trial in PAH-SSc patients Change in PVR 24 weeks Recruiting [19]
 Tocilizumab NCT02676947 Phase II, open-label trial in PAH patients Incidence and severity of adverse events; change in PVR 6 months Recruiting [20]
Therapies targeting mitochondrial dysfunction
 Bardoxolone methyl NCT02036970 Phase II, double-blind, randomised, interventional trial in pulmonary hypertension Group I, II or V patients Change in 6MWD 16 weeks Preliminary results published [21]
NCT02657356 Phase III, double-blind, early interventional trial in PAH-CTD patients Change in 6MWD 24 weeks Recruiting [22]
 GS-4997 NCT02234141 Phase II, dose-ranging, randomised, double-blind, placebo-controlled trial in PAH patients Change in PVR 24 weeks Ongoing, not recruiting [23]
Therapies targeting BMPR2 signalling
 Tacrolimus NCT01647945 Phase II, double-blind, randomised trial in PAH patients Frequency of adverse events 16 weeks Terminated due to limited funding/slow patient recruitment; follow-up multicentre phase IIb efficacy trial planned [24]
Therapies targeting iron deficiency
 Ferinject (ferric carboxymaltose) NCT01447628 Phase II, double-blind, randomised, interventional trial in IPAH, HPAH and anorexigen-associated PAH patients Change in PVR and exercise capacity 24 weeks Recruiting [25]
NCT01847352 Single-blind, nonrandomised, interventional, trial in healthy volunteers who met iron-deficient or iron-replete criteria Change in PASP following i.v. iron infusion 1 week Completed: April 2014 [26, 27]
 Ferrous sulfate (oral dietary  iron supplement) NCT01446848 Interventional, open-label study in IPAH patients with iron deficiency Change in zinc protoporphyrin level; change in serum ferritin level 12 weeks Completed: August 2014 [28]
Pulmonary artery denervation
 Pulmonary arterial denervation procedure chiCTR-ONC-12002085 Phase II, observational, unblinded, nonrandomised study in PAH and PAH-CTD patients Change in PASP and 6MWD 24 weeks Completed: April 2014 [29]
NCT02525926 Single-blind, randomised, interventional efficacy study in PAH patients Mean pulmonary artery pressure 26 weeks Recruiting [30]

PVR: pulmonary vascular resistance (as measured by right heart catheterisation); PAH-SSc: PAH associated with systemic sclerosis; 6MWD: 6-min walk distance; PAH-CTD: PAH associated with connective tissue disease; BMPR2: bone morphogenetic protein receptor type 2; IPAH: idiopathic PAH; HPAH: heritable PAH; PASP: pulmonary artery systolic pressure.