A Study Comparing Abelacimab to Apixaban in the Treatment of Cancer-associated VTE

Eligibility Criteria

• * Male or female subjects ≥18 years old or other legal maturity age according to the country of residence
• * Confirmed diagnosis of cancer (by histology, adequate imaging modality), other than basal-cell or squamous-cell carcinoma of the skin alone with one of the following:
• * Active cancer, defined as either locally active, regionally invasive, or metastatic cancer at the time of randomization and/or
• * Currently receiving or having received anticancer therapy (radiotherapy, chemotherapy, hormonal therapy, any kind of targeted therapy or any other anticancer therapy) in the last 6 months.
• * Confirmed symptomatic or incidental proximal lower limb deep vein thrombosis (DVT) (i.e., popliteal, femoral, iliac, and/or inferior vena cava \[IVC\] thrombosis) and/or a confirmed symptomatic pulmonary embolism (PE), or an incidental PE in a segmental, or larger pulmonary artery.
• * Anticoagulation therapy with a therapeutic dose of DOAC for at least 6 months is indicated
• * Able to provide written informed consent
• * Thrombectomy, insertion of a caval filter or use of a fibrinolytic agent to treat the current (index) DVT and/or PE
• * More than 120 hours of pre-treatment with therapeutic doses of UFH, LMWH, fondaparinux, DOAC, or other anticoagulants
• * An indication to continue treatment with therapeutic doses of an anticoagulant other than that VTE treatment prior to randomization (e.g., atrial fibrillation \[AF\], mechanical heart valve, prior VTE)
• * Platelet count \<50,000/mm3 at the screening visit
• * PE leading to hemodynamic instability (blood pressure \[BP\] \<90 mmHg or shock)
• * Acute ischemic or hemorrhagic stroke or intracranial hemorrhage within the 4 weeks preceding screening
• * Brain trauma or a cerebral or spinal cord surgery or spinal procedures such as lumbar puncture or epidural/spinal anesthesia within 4 weeks of screening
• * Need for aspirin in a dosage of \>100 mg/day or any other antiplatelet agent alone or in combination with aspirin
• * Primary brain cancer or untreated intracranial metastases at baseline
• * Acute myeloid or lymphoid leukemia
• * Bleeding requiring medical attention at the time of randomization or in the preceding 4 weeks
• * Planned brain, spinal cord, cardiac, vascular, major thoracic and/or major abdominal surgery in the 4 weeks following randomization
• * Eastern Cooperative Oncology Group (ECOG) performance status of 3 or 4 at screening
• * Life expectancy \<3 months at randomization
• * Calculated creatinine clearance (CrCl) \<30 mL/min (Cockcroft-Gault equation) at the screening visit
• * Hemoglobin \<8 g/dL at the screening visit
• * Acute hepatitis, chronic active hepatitis, liver cirrhosis; or an alanine aminotransferase (ALT) ≥3 x and/or bilirubin ≥2 x upper limit of normal (ULN) at the screening visit in absence of clinical explanation
• * Uncontrolled hypertension (systolic BP\>180 mm Hg or diastolic BP \>100 mm Hg despite antihypertensive treatment)
• * Women of child-bearing potential (WOCBP) who are unwilling or unable to use highly effective contraceptive measures during the study from screening up to 3 days after last treatment of apixaban or 100 days after administration of abelacimab (See Section 5.3.6. for highly effective contraceptive measures)
• * Sexually active males with sexual partners of childbearing potential must agree to use a condom or other reliable contraceptive measure up to 3 days after last treatment of apixaban or 100 days after administration of abelacimab
• * Pregnant or breast-feeding women
• * Patients known to be receiving strong dual inducers or inhibitors of both CYP3A4 and P gp
• * History of hypersensitivity to any of the study drugs (including apixaban) or excipients, to drugs of similar chemical classes, or any contraindication listed in the label for apixaban
• * Subjects with any condition that in the Investigator's judgement would place the subject at increased risk of harm if he/she participated in the study
• * Use of other investigational (not registered) drugs within 5 half-lives prior to enrollment or until the expected pharmacodynamic(s) (PD) effect has returned to baseline, whichever is longer. Participation in academic non-interventional studies or interventional studies, comprising testing different strategies or different combinations of registered drugs is permitted