Ignite Creation Date:
2024-05-06 @ 4:35 PM
Last Modification Date:
2024-10-26 @ 2:13 PM
Study NCT ID:
NCT05036135
Status:
TERMINATED
Last Update Posted:
2024-06-21
First Post:
2021-08-16
Brief Title:
A Study of AV-101 Dry Powder Inhaled Imatinib in Patients With Pulmonary Arterial Hypertension PAH
Sponsor:
Aerovate Therapeutics
Organization:
Aerovate Therapeutics
Study Overview
Official Title:
IMPAHCT A Phase 2b3 Randomized Double-Blind Placebo-Controlled 24-Week Dose Ranging and Confirmatory Study to Evaluate the Safety and Efficacy of AV-101 in Patients With Pulmonary Arterial Hypertension PAH
Status:
TERMINATED
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
The IMPAHCT study demonstrated that while inhaled imatinib was well tolerated it did not prove to be efficacious at any of the doses of AV-101 evaluated in the study
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
IMPAHCT
Brief Summary:
IMPAHCT Inhaled iMatinib Pulmonary Arterial Hypertension Clinical Trial is a Phase 2bPhase 3 study to evaluate the safety and efficacy of AV-101 dry powder inhaled imatinib in patients with Pulmonary Arterial Hypertension PAH The Phase 2b part of the study will assess three doses to establish an optimal dose for the Phase 3 part of the study The Phase 2b primary endpoint will be the placebo corrected change in pulmonary vascular resistance PVR The Phase 3 primary endpoint will be the placebo corrected change in 6-minute walk distance 6MWD after 24 weeks of treatment
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
True
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
True
Is an FDA AA801 Violation?:
None