Key Insights

Highlights

Success Rate

80% trial completion

Clinical Risk Assessment

Based on trial outcomes

High Risk

Score: 62/100

Termination Rate

4.7%

2 terminated out of 43 trials

Success Rate

80.0%

-6.5% vs benchmark

Late-Stage Pipeline

9%

4 trials in Phase 3/4

Results Transparency

0%

0 of 8 completed with results

Key Signals

80% success

Data Visualizations

Phase Distribution

27Total
Not Applicable (10)
P 1 (7)
P 2 (6)
P 3 (3)
P 4 (1)

Trial Status

Recruiting16
Not Yet Recruiting15
Completed8
Terminated2
Unknown1
Withdrawn1

Trial Success Rate

80.0%

Benchmark: 86.5%

Based on 8 completed trials

Clinical Trials (43)

Showing 20 of 20 trials
NCT07570615Not Yet RecruitingPrimary

Development and Validation of a Chinese Quality of Life Scale for Pulmonary Arterial Hypertension

NCT05967299Phase 1RecruitingPrimary

Study of Intravenous ZMA001 in Healthy Subjects

NCT07318597Phase 2RecruitingPrimary

Study of REGN13335 in Adult Participants With Pulmonary Arterial Hypertension (PAH)

NCT07175038Phase 2RecruitingPrimary

A Study of ROC-101 in Patients With Pulmonary Arterial Hypertension (PAH) and Pulmonary Hypertension Associated With Interstitial Lung Disease (ILD-PH) (ROCSTAR STUDY)

NCT06872112Phase 1RecruitingPrimary

A Study Evaluating the Safety and Tolerability of Artesunate in Patients With Pulmonary Arterial Hypertension

NCT07487441Not Yet RecruitingPrimary

Reverse Remodeling of the Pulmonary Vasculature: a Longitudinal, Investigational Study of the Effects of Sotatercept.

NCT07120789Not ApplicableRecruitingPrimary

Validation of a Patient Knowledge Questionnaire for Pulmonary Hypertension

NCT07457762Not ApplicableRecruitingPrimary

AIRDROP: Can we Improve Adherence to Inhaled Treatment for Pulmonary Arterial Hypertension?

NCT07453030Not Yet RecruitingPrimary

Long-Term Outcomes of Selexipag in Schistosomiasis-Associated Pulmonary Arterial Hypertension

NCT07356375Not Yet RecruitingPrimary

Patient-Reported Outcomes and Adherence After Transition From Inhaled Iloprost to Oral Selexipag in Pulmonary Arterial Hypertension

NCT07172334Not Yet RecruitingPrimary

What is the Role of the Exposome in Pulmonary Hypertension

NCT07368088Phase 1Not Yet RecruitingPrimary

PNEUMOSTEM® for Improving Respiratory Outcomes in Very Premature Infants Diagnosed With Early Pulmonary Arterial Hypertension

NCT07357974Phase 1Not Yet RecruitingPrimary

Impact of Sotatercept on Pulmonary Artery and Right Ventricle Remodeling Imaging Assessed With 68Ga-FAPI PET/CT in Patients With PAH

NCT07314814Not Yet Recruiting

Genetic Hallmarks of Patients With Congenital Portosystemic Shunts and Portopulmonary Hypertension

NCT07266012CompletedPrimary

Incorporating the Venous Excess Ultrasound Score (VExUS Score) Into Contemporary Haemodynamic Risk Assessment in Pulmonary Arterial Hypertension: The INVEXUS-PAH Study

NCT07266519Phase 2Not Yet RecruitingPrimary

SIRIUS - Initial Combination Therapy With an Endothelin Receptor Antagonist, a Phosphodiesterase-5 Inhibitor and Sotatercept in Patients With Newly Diagnosed Pulmonary Arterial Hypertension

NCT07245680Phase 3Not Yet RecruitingPrimary

COMMODITIES Trial: Initial Dual Oral Therapy vs Monotherapy in PAH With Cardiovascular Comorbidities

NCT07207525Not Yet RecruitingPrimary

Information Sources in Pulmonary Hypertension

NCT07013149Recruiting

The Impact of ERA Switching on Risk Stratification in Pulmonary Arterial Hypertension

NCT06998329RecruitingPrimary

PulmonAry hyperteNsion DiagnOsis: a National cohoRt reseArch

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