Bleeding Clinical Trial
Official title:
A Phase II, Double-blind, Parallel Group, Dose-selection Study to Compare Antifibrinolytic MDCO-2010 vs. Placebo and Tranexamic Acid in Reducing Blood Loss in Patients Undergoing Primary Cardiac Surgery
The objective of this study is to determine the dose response relationship regarding blood loss, PK, PD and clinical outcomes of MDCO-2010 in comparison to placebo and tranexamic acid in patients undergoing primary cardiac surgery with cardiopulmonary bypass. The aim of the study is to define minimally effective dose of MDCO-2010.
This was a two-stage, double-blind, randomized, parallel-group, multicenter Phase II
dose-selection study to compare antifibrinolytic MDCO-2010 vs tranexamic acid and placebo in
reducing blood loss.
This study was designed to examine a broad range of doses to fully characterize the
dose-response relationship between MDCO-2010 dose, plasma PK, PD, and clinical effects.
In Stage 1, 90 patients were to be enrolled into one of six treatment groups with 15
patients per group: four groups were to receive MDCO-2010, one group was to receive
tranexamic acid, and one group was to receive placebo. Stage 2 was to be an expansion of
Stage 1.
The study was terminated after 49 patients were enrolled into Stage 1.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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