Intra-articular Bevacizumab for Recurrent Hemarthroses at Target Joints With Chronic Hemophilic Synovitis
Status:
Terminated
Trial end date:
2020-06-30
Target enrollment:
Participant gender:
Summary
Primary Objective The efficacy of intra-articular bevacizumab injection for secondary
prevention of recurrent hemarthroses for hemophilia patients who has had target joints with
chronic synovitis. The safety profiles of intra-articular bevacizumab injection for
hemophilia patients.
Study Population Adult hemophilia patients who have had one or more target joints with
chronic synovitis and recurrent hemarthroses.
Investigational therapy: Intra-articular injection of Bevacizumab (20 or 40 mg/ 0.8 or 1.6
ml/ dose) every month (28 days) for up to 4 months, depending on the improvement of target
joint bleeding.
Study Design The estimated study period is between Jan 2014 and Dec 2015. Totally 10 joints
will be enrolled for this pilot study. Before enrollment, the joint(s) will be evaluated for
their severity both clinically (by 10-point Pain Score, range of motion for the target joint,
and World Federation of Hemophilia Score) and by MRI (using the compatible MRI scales
developed by International Prophylaxis Study Group [IPSG]). Intra-articular injection of
bevacizumab will be administered, after prophylactic factor supplementation, every month for
up to four injections. In the first four patients, 20mg of bevacizumab will be administered.
If there are no Gr 3 or Gr4 dose-limiting toxicities, bevacizumab dose will be escalated to
40mg in the other 6 patients. Before every procedure, the plasma and the synovial fluid
samples will be collected for VEGF quantification for the correlative biomarker study. After
completing the protocol treatment, the efficacy parameters as well as the safety profiles
will be evaluated.