Ongoing clinical study

Comparative study of abelacimab and dalteparin (heparin) with regard to thromboembolism recurrence and bleeding complications in cancer patients with acute venous thromboembolism

MAGNOLIA is a multicenter study investigating the effect of abelacimab compared to dalteparin on venous thromboembolism or bleeding in patients with gastrointestinal or urogenital cancers.

Aim of the study

The study investigates whether abelacimab is non-inferior to dalteparin in preventing thromboembolism recurrence in patients with gastrointestinal/urogenital tumor disease and recent venous thromboembolism. A period of 6 months after study inclusion is examined.

Who can take part?

Adult patients with gastrointestinal/urogenital cancer that cannot be resected surgically, who have suffered an acute venous thromboembolism and require blood thinning with low-molecular-weight heparin.

Procedure

After inclusion in the study, randomization takes place in a 1:1 ratio into a study arm with blood thinning using abelacimab and a study arm with blood thinning using heparin. The duration of therapy is 6 months. During this period, it will be investigated whether the key study endpoints occur (thromboembolism recurrence, bleeding). The examination of the study endpoints is blinded.

Compensation

Original study name

A Multicenter, Randomized, Open-label, Blinded Endpoint Evaluation, Phase 3 Study Comparing the Effect of Abelacimab vs. Dalteparin on Venous Thromboembolism (VTE) Recurrence and Bleeding in Patients With GI/GU Associated VTE

BASEC number

2022-00896

Financial support from

This study is no longer seeking participants. For general questions and further information about the study, please contact us at the address provided.

Verwandte Krankheiten

Responsible Department