Post Marketing Observational Study on Safety of BALFAXAR vs. KCENTRA for Reversal of Vitamin K Antagonist Induced Anticoagulation in Adults Undergoing Urgent Surgery or Invasive Procedure

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorOctapharma

About this trial

Post marketing observational study on safety of BALFAXAR vs. KCENTRA for Reversal of Vitamin K Antagonist Induced Anticoagulation in Adults Undergoing Urgent Surgery or Invasive Procedure

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Subjects at least 18 years of age.

Subjects on VKA treatment.

Received 4F-PCC agent, BALFAXAR or Kcentra, for urgent reversal of within 48 hours prior to urgent surgery or invasive procedure.

Disqualifiers

History of TEE within 90 days before receipt of VKA reversal therapy.

Subjects treated with VKA reversal therapy and not undergoing urgent invasive procedure.

Trial population

Patients at least 18 years of age who are currently on Vitamin K Antagonist treatments and received BALFAXAR or Kcentra for urgent reversal of VKA therapy within 48 hours prior to urgent surgery or invasive procedure. Octapharma will not actively enroll any of the 3,574 projected subjects into the study. Subjects meeting the minimum inclusion and exclusion criteria during the course of routine practice will be added to the study on a monthly basis until the sample size required for the analysis is achieved in each group.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Balfaxar

    Drug

    BALFAXAR (prothrombin complex concentrate, human-lans) is a blood coagulation factor replacement product indicated for the urgent reversal of acquired coagulation factor deficiency induced by Vitamin K antagonist (VKA, e.g., warfarin) therapy in adult patients with need for an urgent surgery/invasive procedure

  • Kcentra

    Drug

    KCENTRA, Prothrombin Complex Concentrate (Human), is a blood coagulation factor replacement product indicated for the urgent reversal of acquired coagulation factor deficiency induced by Vitamin K antagonist (VKA, e.g., warfarin) therapy in adult patients with: * acute major bleeding or * need for an urgent surgery/invasive procedure

Treatment groups

3,574 Participants
are divided into 2 treatment groups
Group A: BALFAXAR® (500 IU)1 intervention
Group B: Kcentra® (500 IU)1 intervention

Trial outcomes

Primary outcomes

1

TEEs within 45 days following VKA reversal treatment

Proportion of subjects diagnosed with TEEs within 45 days following VKA reversal treatment with BALFAXAR compared to proportion of subjects diagnosed with TEEs within the same period following VKA reversal treatment with Kcentra.

Time frame
45 days

Secondary outcomes

1

TEEs within 7 and 14 days following VKA reversal treatment

Proportion of subjects diagnosed with TEEs within 7 and 14 days following VKA reversal treatment with BALFAXAR compared to proportion of subjects diagnosed with TEEs within the same period following VKA reversal treatment with Kcentra.

Time frame
14 days
2

Median Time to TEEs

Median time to TEE following administration of BALFAXAR compared to median time to TEE following administration of Kcentra

Time frame
45 days
3

All Cause Mortality

Proportion of subjects who die from any reason within 7, 14 and 45 days following VKA reversal treatment with BALFAXAR compared to proportion of subjects who die from any reason within the same time period following treatment with Kcentra.

Time frame
45 days
4

Median Time to All Cause Mortality

Median time to death following administration of BALFAXAR compared to median time to death following administration of Kcentra

Time frame
45 days

Other outcomes

Sponsors and contacts

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