Key result
Half-dose apixaban successfully treats VTE without recurrence or bleeding in extreme obesity on cobicistat.
Why the study?
Current guidelines recommend a 50% dose reduction of apixaban for patients receiving strong CYP3A4/P-gp inhibitors regardless of body habitus, but evidence supporting this adjustment in patients with severe obesity (BMI >40 kg/m 2 ) is limited.
Does a 50% dose reduction of apixaban prevent recurrence of thromboembolism without bleeding complications in a patient with severe obesity (BMI >50 kg/m2) receiving a strong CYP3A4/P-gp inhibitor (cobicistat)?
Case Report (n=1)
No
Does a 50% dose reduction of apixaban prevent recurrence of thromboembolism without bleeding complications in a patient with severe obesity (BMI >50 kg/m2) receiving a strong CYP3A4/P-gp inhibitor (cobicistat)?
This case report suggests that guideline-recommended 50% dose reduction of apixaban for concomitant strong CYP3A4/P-gp inhibitor use may be effective and safe even in patients with extreme obesity (BMI >80 kg/m2) treated for venous thromboembolism.
May support reduced-dose apixaban in extreme obesity with cobicistat; hypothesis-generating and should not change practice.
Background/Objective: Current guidelines recommend a 50% dose reduction of apixaban for patients receiving strong CYP3A4/P-glycoprotein (P-gp) inhibitors regardless of body habitus. However, evidence supporting this dose adjustment in patients with severe obesity (BMI >40 kg/m 2 ) is limited. This report describes the use of dose-reduced apixaban for the treatment of venous thromboembolism in a patient with a BMI >50 kg/m 2 receiving a strong CYP3A4/P-gp inhibitor. Summary: A 38-year-old female with a BMI of 81.71 kg/m 2 and a history of HIV on a cobicistat-containing antiretroviral regimen was diagnosed with a left femoral deep vein thromboembolism. She was initially treated with warfarin and enoxaparin bridge therapy but was transitioned to apixaban prior to discharge. Apixaban was initiated at a 50% dose reduction due to the concomitant use of cobicistat, a strong CYP3A4/P-gp inhibitor. The patient successfully completed therapy without recurrence of thromboembolism or bleeding complications. Conclusion: This case demonstrates the successful use of dose-reduced apixaban in a patient with a BMI >50 kg/m 2 receiving a CYP3A4/P-gp inhibitor for the treatment of venous thromboembolism and adds to available literature on apixaban dosing in patients with obesity.
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Womble et al. (2026) conducted a case report in Venous thromboembolism (left femoral deep vein thromboembolism) and severe obesity (n=1). Apixaban was evaluated on Recurrence of thromboembolism or bleeding complications. Apixaban at a 50% dose reduction resulted in successful treatment without VTE recurrence or bleeding in a patient with a BMI of 81.71 kg/m2 taking cobicistat.
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