Tezosentan in Acute Heart Failure (VERITAS 1)
Multicenter, Double-blind, Randomized, Placebo-controlled, Parallel Group Study to Assess the Efficacy, Safety, and Tolerability of Tezosentan in Patients With Acute Heart Failure.
Sponsor: Idorsia Pharmaceuticals Ltd.
Listed as NCT00525707, this PHASE3 trial focuses on Acute Decompensation of Chronic Heart Failure and Acute Heart Failure and remains completed. Sponsored by Idorsia Pharmaceuticals Ltd., it has been updated 8 times since 2003, reflecting limited change activity. This study contributes longitudinal data to the cardiovascular research landscape.
Status Flow
Change History
8 versions recorded-
Sep 2025 — Present [monthly]
Completed PHASE3
-
Sep 2024 — Sep 2025 [monthly]
Completed PHASE3
-
Jul 2024 — Sep 2024 [monthly]
Completed PHASE3
-
Jan 2021 — Jul 2024 [monthly]
Completed PHASE3
-
Aug 2018 — Jan 2021 [monthly]
Completed PHASE3
▶ Show 3 earlier versions
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Jun 2018 — Aug 2018 [monthly]
Completed PHASE3
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Feb 2017 — Jun 2018 [monthly]
Completed PHASE3
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Jan 2017 — Feb 2017 [monthly]
Completed PHASE3
First recorded
Apr 2003
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Idorsia Pharmaceuticals Ltd.
For direct contact, visit the study record on ClinicalTrials.gov .
Study Locations
Aachen, Germany , Ashkelon, Israel , Athens, Greece , Bellevue, United States , Berlin, Germany , Birmingham, United States , Boulogne, France , Bydgoszcz, Poland , Danville, United States , Denver, United States and 24 more locations