Prostacyclin Pathway Therapy for Pulmonary Arterial Hypertension
(WATERLOO Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
Pulmonary arterial hypertension (PAH) is a rare lung disease that leads to elevated blood pressure in the lungs and strain on the right side of the heart. For many years, treatments for PAH have included drugs that target the prostacyclin pathway using intravenous, subcutaneous, oral, and inhaled drugs. These drugs help widen the blood vessels in the lungs so the heart does not have to work as hard. However, these medicines can cause side effects such as jaw pain, flushing, diarrhea, and nausea, and the pump therapy can be very hard to manage day-to-day.
A newer medicine called sotatercept works in a different way. It helps fix some of the root causes of PAH. Early reports suggest that some people do very well on sotatercept and may not need to keep taking their prostacyclin therapy. However, investigators do not yet know if it is safe to stop prostacyclin therapies or how to do so. This study, called WATERLOO, is designed to find out whether slowly stopping prostacyclin therapy while the participant is doing well on sotatercept is safe. Investigators will compare people who stop their prostacyclin therapy to people who keep taking it. This study is being done at PAH expert centres in Canada and Europe.
Who Is on the Research Team?
Dr. Jason Weatherald, MD, MSc, FRCPC
Principal Investigator
University of Alberta
Are You a Good Fit for This Trial?
This trial is for people with pulmonary arterial hypertension (PAH) who are already taking both prostacyclin pathway therapy and sotatercept, and are doing well on these treatments. Participants should be stable enough to consider stopping their prostacyclin medication under medical supervision.Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Trial Overview
The study tests if it is safe for PAH patients doing well on sotatercept to gradually stop their prostacyclin therapy, compared to those who continue it. Participants will either discontinue or keep using their current prostacyclin drugs while staying on sotatercept.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Active Control
Dose de-escalation and discontinuation of parenteral prostacyclins analogues or selexipag
The control group will continue prostacyclin pathway therapies as per their authorized indications, with no change in dosage.
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Alberta
Lead Sponsor
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