A PHASE 3 PROSPECTIVE RANDOMISED CLINICAL TRIAL OF VMX-C001 VS USUAL PHARMACOLOGICAL CARE IN PATIENTS RECEIVING A FXA DIRECT ORAL ANTICOAGULANT (FXA DOAC) WHO REQUIRE URGENT SURGERY OR OTHER INVASIVE PROCEDURE THAT IS ASSOCIATED WITH A HIGH RISK OF BLEEDING, WITH OR WITHOUT PLANNED ADMINISTRATION OF HEPARIN (EQUILIBRIX-S)

Registry ID

VMX-C001-06

Source registry

HEALTH_CANADA

Status

Ongoing

Phase

PHASE3

Study type

INTERVENTIONAL

Sponsor

VARMX B.V.

Start date

2026-07-02

Last update

2025-12-24

Conditions

• SURGERY

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