drugset / Trial / NCT00709865

Study to Assess the Safety and Tolerability of IV Tonapofylline in Subjects With Acute Decompensated Heart Failure (ADHF) and Renal Insufficiency

NCT00709865 ↗

Phase 3 Completed 420 enrolled Biogen
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of the current study is to assess the safety and tolerability of intravenous tonapofylline.

Timeline

Start
2008-07-31
Primary completion
2009-10-30
Completion
2009-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Tonapofylline Small molecule 0.03 mg/kg —
Subject Tonapofylline Small molecule 0.15 mg/kg —
Subject Tonapofylline Small molecule 0.3 mg/kg —