Hemorrhagic Hereditary Telangiectasia Clinical Trial
Official title:
Efficacy and Safety of Bevacizumab for the Treatment Hemorrhagic Hereditary Telangiectasia (HHT) Associated With Severe Hepatic Vascular Malformations. Phase II Study.
The efficacy of anti-VEGF treatments such as Bevacizumab in cases of HHT can be considered
because of the molecular mechanisms implied in angiogenesis and HHT, as well as the
mechanisms of action of this type of treatment. Two articles that have recently reported
spectacular improvement thanks to Bevacizumab in patients with HHT complicated with severe
liver involvement and cardiac effects support us in this sense.
Up to now, the only treatment recommended in the severe hepatic forms of HHT is a liver
transplant, the disadvantages of which are both multiple and well known: long waiting lists,
surgical morbidity and mortality, immunosuppressive treatment for life. Furthermore,
treatment with Bevacizumab is not a contraindication, should the drug be ineffective, for a
subsequent liver transplant if necessary.
n/a
Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
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Completed |
NCT06039124 -
Subsequent Bevacizumab Treatment in Patients With HHT. Follow up BABH
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