Condition (MeSH)
Pulmonary Arterial Hypertension
ClinicalTrials.gov lists 691 trials for Pulmonary Arterial Hypertension or a narrower condition beneath it. Actelion has the most among industry and government lead sponsors, with 59.
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Trials per phase (log scale)
1 more section with rows
691 of the 691 trials are tagged with Pulmonary Arterial Hypertension itself; the rest are tagged with a narrower condition beneath it.
When did Pulmonary Arterial Hypertension trials start? (25)
Shown in this order: most recent first, 1990 onwards. 2026 is partial: trials registered with a 2026 start date so far, not a full year. 2 trials are registered to start in 2027 or later, and not listed here.
Trials over time, by phase
- Phase 1
- Phase 1/2
- Phase 2
- Phase 2/3
- Phase 3
- Phase 4
- Not applicable
- Observational
Top of scale: 40
Trials registered with a start date in each year, 1990 onward, stacked by phase (complete years only; the current partial year is in the table's notes). The table below lists the same counts, most recent years first.
| Year | Trials started |
|---|---|
| 2026 (partial year) | 53 |
| 2025 | 31 |
| 2024 | 31 |
| 2023 | 37 |
| 2022 | 28 |
| 2021 | 39 |
| 2020 | 20 |
| 2019 | 40 |
| 2018 | 38 |
| 2017 | 37 |
Showing 10 of 25 earlier years.
Forecast of the full-year count, planned starts included, not rows of this table: about 61 trials starting in 2026 and about 43 in 2027, the average of the 24 months through September, counted as registered and carried forward, with about 0.7 times the starts already registered for the rest of 2026 added. The rows of this table count trials registered so far with a start date in the year, planned starts included; the forecast looks ahead to the count for the whole year, so it is not the same measure. In backtests on conditions of this size, forecasts made part-way through the year were typically off by about 15 percent and ran about 1 percent high against the count later registered; forecasts made before the year began were off by about 26 percent and ran about 20 percent low against the count later registered. The part-way figures are from forecasts that used a multiple fitted only on earlier years. These figures rest on a few years of history (target years from 2018 to 2025, varying by figure), place each condition as it is mapped today rather than as it was then, and score against a count for the newest year that was still being revised. Only condition series were scored.
Prediction, not a registry value: median of 36 months from start to primary completion across 51 trials still running at the 2026-10-09 snapshot; registered median of 27 months across 441 trials with a primary completion typed Actual. Source: ClinicalTrials.gov / AACT (CTTI), public domain.
What phase are Pulmonary Arterial Hypertension trials in? (9)
Shown in this order: phase order.
Show the trials by phase as a table
| Phase | Trials |
|---|---|
| Phase 1 | 75 |
| Phase 1/2 | 14 |
| Phase 2 | 116 |
| Phase 2/3 | 9 |
| Phase 3 | 104 |
| Phase 4 | 63 |
| Not applicable | 121 |
| Observational | 183 |
| Expanded access | 6 |
How many Pulmonary Arterial Hypertension trials are recruiting? (10)
Shown in this order: the order a trial moves through, from not yet recruiting to unknown.
| Status | Trials |
|---|---|
| Not yet recruiting | 41 |
| Recruiting | 78 |
| Enrolling by invitation | 4 |
| Active, not recruiting | 22 |
| Available | 1 |
Showing 5 of 10 statuses.
Status as registered on ClinicalTrials.gov. Each trial is counted once.
Which lead sponsors run the most Pulmonary Arterial Hypertension trials? (10)
Shown in this order: most trials first. Lead sponsors the registry classes as industry, NIH, US federal, other government or network. A hospital or university the registry files as government can appear here. Sponsors it classes as academic or other are shown on the full page, because that class cannot separate an institution from a named investigator.
| Sponsor | Trials |
|---|---|
| Actelion | 59 |
| United Therapeutics | 44 |
| Bayer | 19 |
| Pfizer's Upjohn has merged with Mylan to form Viatris Inc. | 13 |
| Bial - Portela C S.A. | 12 |
Showing 5 of 10 sponsors.
Which drugs are being tested for Pulmonary Arterial Hypertension? (9)
Shown in this order: most trials first. One row per drug, matched to a single molecule under all its names, ranked by number of trials.
| Drug | Trials |
|---|---|
| Treprostinil | 32 |
| SILDENAFIL | 26 |
| BOSENTAN | 21 |
| Ambrisentan | 18 |
| ILOPROST | 13 |
Showing 5 of 9 drugs.
Interventions as named in the registry (6)
Shown in this order: most trials first.
| Drug | Trials |
|---|---|
| Macitentan Dose 3 | 21 |
| Sotatercept Autoinjector | 17 |
| Tadalafil Pill | 13 |
| Riociguat Pill | 10 |
| BIA 5-1058 | 9 |
Showing 5 of 6 interventions.
These are the names sponsors entered on ClinicalTrials.gov that we have not matched to a single molecule. Some are drugs under a brand or code name; others are procedures, doses or arm labels.
Which serious adverse events do Pulmonary Arterial Hypertension trials report? (10)
Shown in this order: most subjects affected first. Subjects affected summed across trials, a cross-trial signal, not a rate.
| Adverse event | Subjects affected | Trials |
|---|---|---|
| Pneumonia | 646 | 66 |
| Right ventricular failure | 554 | 58 |
| Pulmonary arterial hypertension | 432 | 53 |
| PULMONARY ARTERIAL HYPERTENSION | 416 | 7 |
| Pulmonary hypertension | 381 | 35 |
Showing 5 of 10 adverse events.
Which publications cover Pulmonary Arterial Hypertension? (138)
Shown in this order: major-topic papers first, then newest, then most linked to trials.
| Publication | Journal | Year | Major topic |
|---|---|---|---|
| The Role of Genetics in Congenital Heart Disease-Associated Pulmonary Arterial Hypertension. | Pediatric cardiology | 2026 | Yes |
| A long-term follow-up study of sotatercept for treatment of pulmonary arterial hypertension: interim results of SOTERIA. | The European respiratory journal | 2025 | Yes |
| Sotatercept in Patients with Pulmonary Arterial Hypertension at High Risk for Death. | The New England journal of medicine | 2025 | Yes |
| Macitentan and Tadalafil Combination Therapy in Patients with Pulmonary Arterial Hypertension and Cardiovascular Comorbidities: Real-World Evidence from OPUS and OrPHeUS. | Advances in therapy | 2025 | Yes |
| Seralutinib for the Treatment of Pulmonary Arterial Hypertension in Adults: TORREY Open-Label Extension Study. | Advances in therapy | 2025 | Yes |
Showing 5 of 138 publications.
Prevalence (43)
Shown in this order: jurisdiction, then disease name. Orphanet observation for the mapped ORPHA concept; the mapping relation column says whether that concept is exactly this condition or broader or narrower.
| Orphanet disease | Type | Class | Geography | Jurisdiction | Mapping relation |
|---|---|---|---|---|---|
| Pulmonary arterial hypertension | Point prevalence | 1-9 / 100 000 | United Kingdom | GB | Exact |
| Pulmonary arterial hypertension | Annual incidence | 1-9 / 1 000 000 | United Kingdom | GB | Exact |
| Pulmonary arterial hypertension | Annual incidence | 1-9 / 1 000 000 | United Kingdom | GB | Unspecified |
| Pulmonary arterial hypertension | Annual incidence | 1-9 / 1 000 000 | United Kingdom | GB | Exact |
| Pulmonary arterial hypertension | Point prevalence | 1-9 / 100 000 | United Kingdom | GB | Unspecified |
Showing 5 of 43 prevalence observations.
Rare-disease identity (2)
Shown in this order: exact, broader, narrower, other.
| Orphanet disease | ORPHA code | Relation | Source |
|---|---|---|---|
| Pulmonary arterial hypertension | 182090 | Exact | Orphadata Science knowledge files, Product 1 |
| Pulmonary arterial hypertension | 182090 | Exact | Orphanet Rare Disease Ontology (ORDO) |
Not on this page
Not measured: delivery record.
Checked, with nothing recorded for this condition: sub-conditions in mesh.