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Phase 3 N=216 Randomized Treatment

Efficacy and Safety Study of BERIPLEX® P/N (Kcentra) Compared With Plasma in Patients With Acute Major Bleeding Caused by Anticoagulant Therapy

Blood Coagulation Disorders · Acute Major Bleeding

Enrolled (actual)
216
Serious AEs
27.4%
Results posted
Aug 2013
Primary outcome: Primary: Percentage of Participants Achieving Hemostatic Efficacy of Stopping an Ongoing Major Bleed — 72.4; 65.4 percentage of participants

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Beriplex® P/N (Kcentra) (Biological); Fresh frozen plasma (Biological)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
CSL Behring
Primary completion
Nov 2010

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants Achieving Hemostatic Efficacy of Stopping an Ongoing Major Bleed
72.4; 65.4
PRIMARY
Percentage of Participants Who Had a Rapid Decrease of the International Normalized Ratio (INR)
62.2; 9.6
SECONDARY
Percentage of Participants Who Had Hemostatic Efficacy for Visible or Non-visible Musculoskeletal Bleeding
73.5; 67.3
SECONDARY
Incremental in Vivo Recovery (IVR) (Response) of Factors II, VII, IX, and X, Protein C, and Protein S for Beriplex
2.00; 2.15; 1.29; 1.96; 2.04; 2.17
SECONDARY
Plasma Levels of Factors II, VII, IX, and X, Protein C, and Protein S
20.1; 22.3; 87.5; 31.9; 77.1; 58.1
SECONDARY
Percentage of Participants With INR Correction at Various Times After the Start of Infusion
4; 0; 69; 0; 71; 9
SECONDARY
Percentage of Participants With INR Correction at Various Times After Randomization
59; 2; 67; 2; 76; 10
SECONDARY
Transfusion of Red Blood Cells
1.4; 1.2
SECONDARY
Use of Other Blood Products and Hemostatic Agents
0.3; 0.3
SECONDARY
45-Day All-cause Mortality
9; 5
SECONDARY
Overall Treatment-emergent Adverse Events (TEAEs)
66; 71; 10; 23; 32; 26

Summary

The purpose of this study is to evaluate efficacy, safety and tolerance of BERIPLEX® P/N (Kcentra) compared with plasma in regard to rapid reversal of coagulopathy induced by coumarin derivatives in subjects who require immediate correction of INR (International Normalized Ratio)and to stop an acute major bleeding.

Eligibility Criteria

Inclusion Criteria

  • Male and female subjects ≥ 18 years
  • Subjects who have received oral vitamin K-antagonist therapy
  • Subjects who have acute major bleeding, defined as one of the following: life-threatening or potentially life-threatening, acute bleeding associated with a fall in hemoglobin (Hb) level ≥ 2g/dL, bleeding requiring blood product transfusion
  • INR ≥ 2 within 3 hours before start of study treatment
  • Informed consent has been obtained

Exclusion Criteria

  • Expected survival of less than 3 days, or expected surgery in less than 1 day
  • Acute trauma for which reversal of vitamin K antagonists alone would not be expected to control the acute bleeding event
  • Use of unfractionated or low molecular weight heparin use from 24 hours prior to enrollment or expected need within 24 hours after start of infusion
  • For patients with ICH: Glasgow coma score (GCS) 30cc as assessed by ABC/21; for subdural hematomas: maximum thickness ≥ 10 mm, midline shift ≥ 5 mm; for subarachnoid hemorrhage: any evidence of hydrocephalus; infratentorial ICH location; epidural hematomas; intraventricular extension of hemorrhage; modified Rankin score (mRS) of >3 prior to ICH
  • History of thrombotic event, myocardial infarction, disseminated intravascular coagulation, cerebral vascular accident, transient ischemic attack, unstable angina pectoris, or severe peripheral vascular disease within 3 months of enrollment
  • Known history of antiphospholipid antibody syndrome or lupus anticoagulant antibodies
  • Suspected or confirmed sepsis at time of enrollment
  • Administration of whole blood, plasma, plasma fractions or platelets within 2 weeks prior to inclusion into the study
  • Large blood vessel rupture (e.g. in advanced cancer patient)
  • Pre-existing progressive fatal disease with a life expectancy of less than 2 months
  • Known inhibitors to coagulation factors II, VII, IX, or X; or hereditary protein C or protein S deficiency; or heparin-induced, type II thrombocytopenia
  • Treatment with any other investigational medicinal product within 30 days prior to inclusion into the study
  • Presence or history of hypersensitivity to components of the study medication
  • Pregnant or breast-feeding women
  • Prior inclusion in this study or any other CSL Behring-sponsored Beriplex study
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00708435). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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