A Study of Andexanet Alfa in Patients Requiring Urgent Surgery or Procedure

Phase 3

Withdrawn

• Conditions: Urgent Surgery
• Interventions: Drug: Andexanet alfa; Drug: Usual Care

• Registration Number: NCT05926349
• Lead Sponsor: AstraZeneca

Brief Summary

The study will aim to find out if the drug andexanet alfa is safe and effective in preventing major bleeding during urgent surgery or invasive procedures. The study will compare the use of andexanet alfa to the usual care given at the study center.

Detailed Description

This study will be an open-label, randomised, controlled, prospective, multicenter study. The study will include patients requiring urgent surgery or procedure that needs to be performed within 15 hours of the last dose of blood-thinning drug (direct oral activated Factor X (FXa) inhibitor).

The study will comprise of the following periods:

* Screening, followed by surgery or procedure and study intervention.

* Follow-up period: there will be four follow-up visits over a duration of approximately 30 days.

* Follow-up visit for patients with positive anti-andexanet alfa antibody test: patients with a positive anti-andexanet alfa antibody response at day 30 will have a follow-up anti-andexanet alfa antibody test approximately 120 days post-surgery or procedure.

Patients will be randomised in the ratio of 1:1 to receive either andexanet alfa or usual care.

Study Timeline

• Study First Submitted: 2023-06-09
• Study First Submitted QC: 2023-06-21
• Study First Posted: 2023-07-03
• Study Start: 2024-08-02
• Status Verified: 2024-10
• Last Update Submitted: 2024-10-23
• Last Update Posted: 2024-10-26
• Primary Completion: 2027-01-05
• Study Completion: 2027-09-07

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: 800

Inclusion Criteria

• The patient requires, in the opinion of the Investigator, urgent surgery or procedure and requires reversal of direct oral FXa inhibition.
• The patient requires urgent surgery or procedure within 12 hours of informed consent.
• The patient requires urgent surgery or procedure that is expected to be associated with a high risk of bleeding or bleeding to occur into a critical organ.
• The patient has taken an oral FXa inhibitor (such as apixaban, rivaroxaban, or edoxaban) within 15 hours or more, prior to start of surgery or procedure.
• Female patients of childbearing potential must have a negative pregnancy test at Screening.
• Willingness to use highly effective methods of contraception (for male and female patients who are fertile).

Exclusion Criteria

• The patient requires surgeries or procedures that have a very low chance of causing significant, uncontrollable bleeding, such as small skin procedures, cataract surgery, and minor dental procedures.
• The patient has acute life-threatening bleeding at the time of Screening.
• The patient will undergo a surgery or procedure which will require the use of heparin.
• Patient who is not expected to live for more than three months due to other health problems or has specifically requested not to be resuscitated if their heart stops beating.
• Prior to screening, the patient had either experienced low platelet count due to heparin use with or without blood clots or had a genetic condition that affects blood clotting.
• Patient has acute decompensated heart failure, cardiogenic shock, sepsis, or septic shock at the time of Screening.
• Patient has history of heparin-induced thrombocytopenia (with or without thrombosis) or inherited coagulopathy (eg, anti-thrombin III deficiency, anti-phospholipid antibody syndrome, protein C/S deficiency, Factor V Leiden) at the time of Screening.
• Previously diagnosed with a bleeding disorder (eg, platelet function disorder, hemophilia, Von Willebrand disease, or coagulation factor deficiency).
• Prior known hypersensitivity to andexanet alfa.
• Use of andexanet alfa 30 days prior to Screening.
• Patient diagnosed with dementia.
• Any prohibited medication as determined in the study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Andexanet Alfa Group	Andexanet alfa	Patients will receive andexanet alfa as IV bolus followed by an infusion.
Usual Care Group	Usual Care	Patients will receive treatment based on the Investigator's discretion, according to regional, local/institutional guidelines or practices.

Primary Outcome Measures

Name	Time	Method
Number of patients achieving effective intraoperative hemostasis	From start to the end of surgery or procedure on Day 0	Intraoperative hemostasis will be assessed according to the categories as per 4-point hemostasis scale: Excellent - Normal hemostasis, Good - Mildly abnormal hemostasis (eg. slight oozing from surgical wounds), Moderate - Moderate abnormality in intraprocedural hemostasis (eg. controllable bleeding), Poor - Severe hemostatic abnormality (eg. severe refractory hemorrhage). Hemostasis will be considered to be effective if the intraoperative hemostasis category is 'excellent' or 'good', and ineffective if the intraoperative hemostasis category is 'moderate' or 'poor'.

Secondary Outcome Measures

Name	Time	Method
Change from Baseline in anti-FXa activity measured through blood samples	Baseline to two hours post start of surgery or procedure	The ability of andexanet alfa to sustainably reverse the anticoagulation effect of FXa inhibitors by reduction of anti-FXa activity when compared to usual care at two hours post start of surgery or procedure will be assessed.

Trial Locations

Locations (1)

Research Site; 🇬🇧 London, United Kingdom