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Soluble Guanylate Cyclase Stimulators
Combo Riociguat and Ambrisentan Therapy for Pulmonary Hypertension
Phase 4
Waitlist Available
Led By Naushad Hirani, MD
Research Sponsored by University of Calgary
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 and 12 months
Awards & highlights
Study Summary
To evaluate the safety and efficacy of first-line combination therapy using riociguat with ambrisentan in patients with Pulmonary Arterial Hypertension (PAH).
Eligible Conditions
- Pulmonary Hypertension
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4 and 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 and 12 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Pulmonary Vascular resistance
Secondary outcome measures
Clinical worsening
Dyspnea
Echocardiographic parameters
+7 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: Combo Riociguat and Ambrisentan TherapyExperimental Treatment1 Intervention
Riociguat Oral Product and Ambrisentan Oral Product to be given in combination to de novo (untreated) patients.
Find a Location
Who is running the clinical trial?
University of CalgaryLead Sponsor
792 Previous Clinical Trials
869,134 Total Patients Enrolled
BayerIndustry Sponsor
2,240 Previous Clinical Trials
25,332,757 Total Patients Enrolled
Naushad Hirani, MDPrincipal InvestigatorUniversity of Calgary
1 Previous Clinical Trials
12 Total Patients Enrolled
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