Positioning Imatinib for Pulmonary Arterial Hypertension
NCT04416750 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 17
Last updated 2023-10-10
Summary
Pulmonary Arterial Hypertension (PAH) is a rare condition in which a narrowing of blood vessels carrying blood through the lungs puts an increased work load on the heart; it has to work harder to pump blood through the lungs. While current treatments relieve some of the symptoms, they do not stop or reverse the disease in the affected blood vessels. Imatinib is a medicine licensed for some types of cancers. A published study has shown that imatinib can have beneficial effects on blood flow through the lungs and exercise capacity in patients with PAH, even when added to existing treatments. However, there have been concerns about its safety and tolerability. Imatinib continues to be prescribed occasionally on compassionate grounds, usually when other treatment options have been exhausted, and some patients feel better on the drug. To improve the investigator's understanding, the investigators of this study re-visits the use of Imatinib as a potential treatment for patients with PAH.
Conditions
Interventions
- DRUG
-
Imatinib Mesylate
Treatment with Imatinib
Sponsors & Collaborators
-
National Institute for Health Research, United Kingdom
collaborator OTHER_GOV - collaborator OTHER_GOV
- collaborator OTHER
-
University of Sheffield
collaborator OTHER -
Imperial College London
lead OTHER
Principal Investigators
-
Martin R Wilkins, MD, FRCP · Imperial College London
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-01-20
- Primary Completion
- 2024-07-01
- Completion
- 2024-07-01
Countries
- United Kingdom
Study Locations
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