CompletedPhase 2

Efficacy of Nintedanib Per os as a Treatment for Epistaxis in HHT Disease.

France61 participantsStarted 2020-06-22

Plain-language summary

The recognized manifestations of HHT are all due to abnormalities in vascular structure. Epistaxis are spontaneous, very variable, may occur as often as several times every day, and are recurrent in 90% of patients and associated with chronic and severe anemia in 2-10%. They also significantly reduce quality of life. Blood transfusions are sometimes required in 10-30% of patients. Previous studies showed that antiangiogenic treatments such as anti-VEGF treatment (bevacizumab) administered intravenously was efficient on epistaxis and dramatically reduced nosebleeds. Tyrosine kinase inhibitors are anti-angiogenic molecules which are available orally and could therefore overcome the difficulties encountered with bevacizumab. The investigator hypothesized that nintedanib, acting by indirect inhibition of the VEGF receptor should allow a reduction of epistaxis in HHT patient. Nintedanib has been used in one HHT patient following the diagnosis of Insterstitial Pulmonary Fibrosis (published case report in 2017, Kovacs et al) with encouraging results. The aim is to evaluate efficacy of nintedanib for the treatment of epistaxis in HHT patients

Who can participate

Age range18 Years

SexALL

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Inclusion Criteria: * Age \> 18 years old * Patients who have given their free informed and signed consent * Patients affiliated to a social security scheme or similar * Patients monitored for clinically confirmed HHT and/or with molecular biology confirmation * Patient with an Epistaxis Severity Score (ESS) \> 4 Exclusion Criteria: * Pregnant woman or woman of child bearing potential * Woman who are breast feeding. * Patient who is protected adults under the terms of the law (French Public Health Code). * Participation in another interventional clinical trial which may interfere with the proposed trial * Active infection. * (AST, ALT \> 1,5 fold upper limit of normal (ULN) and/or Bilirubin \> 1,5 fold upper limit of normal (ULN). * Severe renal impairment * Presence of non-treated pulmonary arteriovenous malformations accessible to a treatment on CT scan within 5 years. * Patients with hemoptysis or hematuria within 12 weeks prior to inclusion. * Patients with active gastro-intestinal (GI) bleeding or GI ulcers within 12 months prior to inclusion. * Presence of cerebral arteriovenous malformation. * Patients who require full-dose therapeutic anticoagulation (e.g. vitamin K antagonist or heparin, dabigatran) or high dose antiplatelet therapy, , patients under anticoagulation with rivaroxaban, apixaban and epixaban. * Patients with P-glycoprotein (P-gp) substrates/inducers/inhibitors (e.g.: ketoconazole, erythromycin, cyclosporine, rifampicin, carbamazepine, phenytoin, and …

What they're measuring

Epistaxis duration assessed on epistaxis grids completed by the patients.

Timeframe: 12 weeks

Trial details

NCT IDNCT03954782

SponsorHospices Civils de Lyon

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-02-24